Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51705 |
| ensemblid | ENSG00000164035.10 |
| hgncid | 16041 |
| symbol | EMCN |
| name | endomucin |
| refseq_nuc | NM_016242.4 |
| refseq_prot | NP_057326.2 |
| ensembl_nuc | ENST00000296420.9 |
| ensembl_prot | ENSP00000296420.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 100395341 |
| end | 100518022 |
| strand | - |
| ver | v1.2 |
| region | chr4:100395341-100518022 |
| region5000 | chr4:100390341-100523022 |
| regionname0 | EMCN_chr4_100395341_100518022 |
| regionname5000 | EMCN_chr4_100390341_100523022 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 261 | 166 | 63 | 40 | 31 | 7 | 23 | 20 | EMCN_chr4_100390341_100523022 | EMCN | MELLQ others(256): Show |
chr4 | 100390341 | 100523022 |
| a0002 | 0/0 | 260 | 89 | 18 | 24 | 35 | 0 | 12 | 26 | EMCN_chr4_100390341_100523022 | EMCN | MELLQ others(255): Show |
chr4 | 100390341 | 100523022 |
| a0003 | 0/0 | 261 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | MELLQ others(256): Show |
chr4 | 100390341 | 100523022 |
| a0004 | 0/0 | 261 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | MELLQ others(256): Show |
chr4 | 100390341 | 100523022 |
| a0005 | 0/0 | 261 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | MELLQ others(256): Show |
chr4 | 100390341 | 100523022 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 783 | 163 | 60 | 40 | 31 | 7 | 23 | EMCN_chr4_100390341_100523022 | EMCN | ATGGA others(778): Show |
chr4 | 100390341 | 100523022 | ||
| a0001c0004 | 0/0 | 783 | 2 | 2 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ATGGA others(778): Show |
chr4 | 100390341 | 100523022 | ||
| a0001c0008 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ATGGA others(778): Show |
chr4 | 100390341 | 100523022 | ||
| a0002c0002 | 0/0 | 780 | 88 | 17 | 24 | 35 | 0 | 12 | EMCN_chr4_100390341_100523022 | EMCN | ATGGA others(775): Show |
chr4 | 100390341 | 100523022 | ||
| a0002c0006 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ATGGA others(775): Show |
chr4 | 100390341 | 100523022 | ||
| a0003c0003 | 0/0 | 783 | 4 | 3 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ATGGA others(778): Show |
chr4 | 100390341 | 100523022 | ||
| a0004c0005 | 0/0 | 783 | 2 | 0 | 1 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ATGGA others(778): Show |
chr4 | 100390341 | 100523022 | ||
| a0005c0007 | 0/0 | 783 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | ATGGA others(778): Show |
chr4 | 100390341 | 100523022 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3968 | 7 | 0 | 0 | 6 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3963): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0002 | 0/0 | 3967 | 65 | 8 | 24 | 15 | 6 | 12 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3962): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0003 | 1/0 | 3966 | 18 | 6 | 5 | 5 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3961): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0004 | 0/0 | 3968 | 10 | 9 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3963): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0005 | 0/0 | 3967 | 14 | 13 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3962): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0006 | 0/0 | 3966 | 12 | 2 | 2 | 3 | 0 | 5 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3961): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0007 | 0/0 | 3965 | 4 | 3 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3960): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0008 | 0/0 | 3965 | 5 | 4 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3960): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0009 | 0/0 | 3966 | 4 | 4 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3961): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0011 | 0/0 | 3968 | 4 | 4 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3963): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0012 | 0/0 | 3968 | 3 | 0 | 2 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3963): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0013 | 0/1 | 3967 | 3 | 0 | 1 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3962): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0015 | 0/0 | 3969 | 2 | 2 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3964): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0018 | 0/0 | 3966 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3961): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0019 | 0/0 | 3966 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3961): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0020 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3962): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0023 | 0/0 | 3968 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3963): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0027 | 0/0 | 3968 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3963): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0028 | 0/0 | 3968 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3963): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0029 | 0/0 | 3966 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3961): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0030 | 0/0 | 3966 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3961): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0032 | 0/0 | 3967 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3962): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0033 | 0/0 | 3967 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3962): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0034 | 0/0 | 3965 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3960): Show |
chr4 | 100390341 | 100523022 |
| a0001c0001t0038 | 0/0 | 3966 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3961): Show |
chr4 | 100390341 | 100523022 |
| a0001c0004t0004 | 0/0 | 3968 | 2 | 2 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3963): Show |
chr4 | 100390341 | 100523022 |
| a0001c0008t0005 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3962): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0001 | 0/0 | 3965 | 61 | 7 | 18 | 27 | 0 | 9 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3960): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0003 | 0/0 | 3963 | 3 | 0 | 1 | 2 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3958): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0004 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3960): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0006 | 0/0 | 3963 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3958): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0007 | 0/0 | 3962 | 6 | 4 | 2 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3957): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0009 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3958): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0010 | 0/0 | 3966 | 4 | 0 | 2 | 1 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3961): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0014 | 0/0 | 3965 | 2 | 0 | 0 | 2 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3960): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0016 | 0/0 | 3966 | 2 | 2 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3961): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0021 | 0/0 | 3965 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3960): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0022 | 0/0 | 3966 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3961): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0024 | 0/0 | 3965 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3960): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0025 | 0/0 | 3965 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3960): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0026 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3960): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0031 | 0/0 | 3965 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3960): Show |
chr4 | 100390341 | 100523022 |
| a0002c0002t0037 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3958): Show |
chr4 | 100390341 | 100523022 |
| a0002c0006t0004 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3960): Show |
chr4 | 100390341 | 100523022 |
| a0003c0003t0002 | 0/0 | 3967 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3962): Show |
chr4 | 100390341 | 100523022 |
| a0003c0003t0004 | 0/0 | 3968 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3963): Show |
chr4 | 100390341 | 100523022 |
| a0003c0003t0035 | 0/0 | 3966 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3961): Show |
chr4 | 100390341 | 100523022 |
| a0003c0003t0036 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3960): Show |
chr4 | 100390341 | 100523022 |
| a0004c0005t0017 | 0/0 | 3966 | 2 | 0 | 1 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3961): Show |
chr4 | 100390341 | 100523022 |
| a0005c0007t0002 | 0/0 | 3967 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | ACATT others(3962): Show |
chr4 | 100390341 | 100523022 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0214 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0008g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0011g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0011g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0011g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0012g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0012g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0012g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0013g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0013g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0013g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0015g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0015g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0018g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0019g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0020g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0023g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0027g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0028g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0029g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0030g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0032g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0033g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0034g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0001t0038g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0004t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0004t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0001c0008t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0006g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0007g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0007g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0010g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0010g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0010g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0010g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0014g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0014g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0016g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0016g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0021g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0022g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0024g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0025g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0026g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0031g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0002t0037g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0002c0006t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0003c0003t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0003c0003t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0003c0003t0035g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0003c0003t0036g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0004c0005t0017g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0004c0005t0017g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| a0005c0007t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | CHS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | CHS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | CHS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0142 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0258 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00673 | hp1 | a0001 | c0001 | t0033 | g0141 | EAS | CHS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | CHS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00735 | hp1 | a0004 | c0005 | t0017 | g0020 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00741 | hp1 | a0001 | c0001 | t0027 | g0247 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01070 | hp1 | a0002 | c0002 | t0007 | g0163 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0200 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01071 | hp1 | a0002 | c0002 | t0007 | g0164 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01074 | hp2 | a0002 | c0002 | t0003 | g0047 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01106 | hp1 | a0001 | c0001 | t0012 | g0026 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0144 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01167 | hp1 | a0003 | c0003 | t0002 | g0172 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0091 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0117 | AMR | PUR | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0143 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01361 | hp1 | a0001 | c0001 | t0013 | g0246 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01496 | hp2 | a0002 | c0002 | t0010 | g0148 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0127 | EUR | IBS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01515 | hp2 | a0004 | c0005 | t0017 | g0019 | EUR | IBS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0187 | EUR | IBS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0129 | EUR | IBS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0041 | EUR | IBS | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0256 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01975 | hp1 | a0001 | c0001 | t0007 | g0125 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01975 | hp2 | a0001 | c0001 | t0029 | g0159 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01981 | hp1 | a0002 | c0002 | t0010 | g0145 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02027 | hp1 | a0001 | c0001 | t0023 | g0005 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0128 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02071 | hp1 | a0002 | c0002 | t0010 | g0089 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0149 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | KHV | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02145 | hp1 | a0001 | c0001 | t0019 | g0155 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0116 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02148 | hp1 | a0001 | c0001 | t0012 | g0180 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02257 | hp2 | a0002 | c0006 | t0004 | g0048 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0208 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0121 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0056 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0235 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02615 | hp2 | a0003 | c0003 | t0036 | g0160 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02630 | hp2 | a0001 | c0004 | t0004 | g0249 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0064 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02717 | hp2 | a0002 | c0002 | t0007 | g0168 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0052 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0133 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02809 | hp2 | a0001 | c0004 | t0004 | g0248 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02818 | hp1 | a0003 | c0003 | t0004 | g0158 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0244 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02896 | hp1 | a0003 | c0003 | t0035 | g0198 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02896 | hp2 | a0001 | c0001 | t0028 | g0175 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0124 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02922 | hp2 | a0002 | c0002 | t0016 | g0111 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02970 | hp1 | a0002 | c0002 | t0016 | g0110 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02970 | hp2 | a0002 | c0002 | t0007 | g0165 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02976 | hp1 | a0002 | c0002 | t0007 | g0167 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0173 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0081 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0151 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0112 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03139 | hp1 | a0002 | c0002 | t0037 | g0123 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03139 | hp2 | a0001 | c0001 | t0030 | g0190 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0109 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03209 | hp2 | a0002 | c0002 | t0009 | g0171 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03225 | hp1 | a0001 | c0001 | t0020 | g0023 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0022 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0132 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03486 | hp2 | a0002 | c0002 | t0026 | g0049 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03491 | hp1 | a0005 | c0007 | t0002 | g0209 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0051 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0050 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | ESN | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0120 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0107 | AFR | GWD | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0170 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0126 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03669 | hp1 | a0001 | c0001 | t0032 | g0254 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03669 | hp2 | a0001 | c0001 | t0018 | g0219 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0057 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0147 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0098 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03704 | hp2 | a0001 | c0001 | t0006 | g0152 | SAS | PJL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | BEB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03831 | hp2 | a0002 | c0002 | t0010 | g0090 | SAS | BEB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | BEB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03942 | hp1 | a0001 | c0001 | t0034 | g0140 | SAS | BEB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | BEB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG04115 | hp2 | a0002 | c0002 | t0022 | g0234 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0134 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG04204 | hp1 | a0002 | c0002 | t0006 | g0053 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG04204 | hp2 | a0001 | c0001 | t0013 | g0008 | SAS | STU | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0242 | AFR | YRI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0113 | AFR | YRI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | CHB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | CHB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18906 | hp1 | a0001 | c0008 | t0005 | g0197 | AFR | YRI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0153 | AFR | YRI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18946 | hp1 | a0002 | c0002 | t0025 | g0059 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18973 | hp2 | a0002 | c0002 | t0024 | g0095 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18980 | hp1 | a0002 | c0002 | t0014 | g0096 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18984 | hp2 | a0002 | c0002 | t0003 | g0083 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0130 | AFR | LWK | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0250 | AFR | LWK | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19043 | hp1 | a0002 | c0002 | t0004 | g0162 | AFR | LWK | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | LWK | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19056 | hp2 | a0002 | c0002 | t0003 | g0082 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19060 | hp1 | a0002 | c0002 | t0014 | g0137 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19084 | hp2 | a0002 | c0002 | t0021 | g0063 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19087 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0191 | AFR | YRI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | YRI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20129 | hp1 | a0002 | c0002 | t0007 | g0166 | AFR | ASW | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ASW | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20752 | hp1 | a0001 | c0001 | t0012 | g0238 | EUR | TSI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | TSI | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0065 | SAS | GIH | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0226 | SAS | GIH | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01123 | hp1 | a0002 | c0002 | t0031 | g0138 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0189 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02486 | hp1 | a0001 | c0001 | t0038 | g0211 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0114 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0174 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0243 | AFR | ACB | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0119 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | MSL | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | USA | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| HG06807 | hp2 | a0001 | c0001 | t0015 | g0115 | AFR | USA | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0118 | AFR | USA | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | USA | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | LWK | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | LWK | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0013 | g0009 | REF | REF | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0214 | REF | REF | EMCN_chr4_100390341_100523022 | EMCN | chr4 | 100390341 | 100523022 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:100410282 | G | A | 1 | a0002 | 1 | HG03139.hp1 | splice_region_variant | LOW | c.*39C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/12 | chr4 | 100410282 | |||||||
| chr4:100465486 | C | T | 1 | a0003 | 4 | HG01167.hp1 HG02615.hp2 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.313G>A | p.Val105Ile | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/12 | 421/3966 | 313/786 | 105/261 | chr4 | 100465486 | |||
| chr4:100465500 | G | A | 1 | a0004 | 2 | HG00735.hp1 HG01515.hp2 |
missense_variant | MODERATE | c.299C>T | p.Ser100Phe | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/12 | 407/3966 | 299/786 | 100/261 | chr4 | 100465500 | |||
| chr4:100479949 | A | G | 1 | a0005 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.155T>C | p.Val52Ala | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/12 | 263/3966 | 155/786 | 52/261 | chr4 | 100479949 | |||
| chr4:100480004 | TAAC | T | 1 | a0002 | 89 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(86): Show |
conservative_inframe_deletion | MODERATE | c.97_99delGTT | p.Val33del | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/12 | 207/3966 | 97/786 | 33/261 | chr4 | 100480004 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:100415923 | G | A | 1 | a0001c0008 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.726C>T | p.Thr242Thr | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/12 | 834/3966 | 726/786 | 242/261 | chr4 | 100415923 | |||
| chr4:100465487 | G | A | 2 | a0001c0004 a0002c0006 |
3 | HG02257.hp2 HG02630.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.312C>T | p.Asn104Asn | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/12 | 420/3966 | 312/786 | 104/261 | chr4 | 100465487 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:100395441 | A | G | 2 | a0001c0001t0013 a0001c0001t0027 |
3 | HG00741.hp1 HG01361.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2972T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 14880 | chr4 | 100395441 | ||||||
| chr4:100395693 | G | A | 3 | a0001c0001t0007 a0001c0001t0008 a0002c0002t0007 |
15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2720C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 14628 | chr4 | 100395693 | ||||||
| chr4:100395723 | G | T | 1 | a0002c0002t0024 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2690C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 14598 | chr4 | 100395723 | ||||||
| chr4:100395742 | C | G | 1 | a0001c0001t0023 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2671G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 14579 | chr4 | 100395742 | ||||||
| chr4:100396017 | A | T | 10 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0015 others(7): Show |
25 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2396T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 14304 | chr4 | 100396017 | ||||||
| chr4:100396027 | C | G | 1 | a0001c0001t0011 | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2386G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 14294 | chr4 | 100396027 | ||||||
| chr4:100396052 | T | A | 1 | a0002c0002t0025 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2361A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 14269 | chr4 | 100396052 | ||||||
| chr4:100396332 | T | G | 16 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0011 others(13): Show |
44 | HG01070.hp2 HG01109.hp2 HG01884.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2081A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13989 | chr4 | 100396332 | ||||||
| chr4:100396363 | C | A | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(40): Show |
231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*2050G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13958 | chr4 | 100396363 | ||||||
| chr4:100396486 | A | G | 1 | a0001c0001t0018 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1927T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13835 | chr4 | 100396486 | ||||||
| chr4:100396538 | T | C | 1 | a0001c0001t0011 | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1875A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13783 | chr4 | 100396538 | ||||||
| chr4:100396539 | C | CT | 1 | a0001c0001t0011 | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1873_*1874insA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13781 | chr4 | 100396539 | ||||||
| chr4:100396540 | C | CT | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(17): Show |
165 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*1872dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13780 | chr4 | 100396540 | ||||||
| chr4:100396540 | C | CTT | 11 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0015 others(8): Show |
28 | HG00741.hp1 HG01106.hp1 HG01109.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1871_*1872dupAA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13780 | chr4 | 100396540 | ||||||
| chr4:100396540 | C | T | 1 | a0001c0001t0011 | 4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1873G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13781 | chr4 | 100396540 | ||||||
| chr4:100396540 | CT | C | 5 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0034 others(2): Show |
17 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1872delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13780 | chr4 | 100396540 | ||||||
| chr4:100396604 | G | A | 1 | a0002c0002t0026 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1809C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13717 | chr4 | 100396604 | ||||||
| chr4:100396637 | G | A | 1 | a0002c0002t0037 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1776C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13684 | chr4 | 100396637 | ||||||
| chr4:100396653 | G | T | 5 | a0001c0001t0006 a0001c0001t0033 a0001c0001t0034 others(2): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1760C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13668 | chr4 | 100396653 | ||||||
| chr4:100396692 | G | A | 3 | a0001c0001t0007 a0001c0001t0008 a0002c0002t0007 |
15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1721C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13629 | chr4 | 100396692 | ||||||
| chr4:100396771 | A | AT | 11 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0015 others(8): Show |
26 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1641dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13549 | chr4 | 100396771 | ||||||
| chr4:100396806 | T | G | 10 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0015 others(7): Show |
25 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1607A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13515 | chr4 | 100396806 | ||||||
| chr4:100396807 | G | T | 1 | a0002c0002t0021 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1606C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13514 | chr4 | 100396807 | ||||||
| chr4:100396891 | A | G | 11 | a0001c0001t0001 a0001c0001t0023 a0002c0002t0001 others(8): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1522T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13430 | chr4 | 100396891 | ||||||
| chr4:100396942 | C | CT | 11 | a0001c0001t0001 a0001c0001t0023 a0002c0002t0001 others(8): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1470dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13378 | chr4 | 100396942 | ||||||
| chr4:100396942 | CT | C | 8 | a0001c0001t0004 a0001c0001t0019 a0001c0001t0020 others(5): Show |
18 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1470delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13378 | chr4 | 100396942 | ||||||
| chr4:100397015 | T | G | 6 | a0001c0001t0005 a0001c0001t0028 a0001c0001t0029 others(3): Show |
19 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1398A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13306 | chr4 | 100397015 | ||||||
| chr4:100397108 | C | T | 11 | a0001c0001t0001 a0001c0001t0023 a0002c0002t0001 others(8): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1305G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13213 | chr4 | 100397108 | ||||||
| chr4:100397205 | T | C | 1 | a0003c0003t0035 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1208A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 13116 | chr4 | 100397205 | ||||||
| chr4:100397480 | G | A | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(42): Show |
236 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*933C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12841 | chr4 | 100397480 | ||||||
| chr4:100397695 | G | C | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(42): Show |
236 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*718C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12626 | chr4 | 100397695 | ||||||
| chr4:100397768 | T | C | 1 | a0002c0002t0031 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*645A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12553 | chr4 | 100397768 | ||||||
| chr4:100397946 | C | G | 8 | a0001c0001t0004 a0001c0001t0019 a0001c0001t0020 others(5): Show |
19 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*467G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12375 | chr4 | 100397946 | ||||||
| chr4:100398008 | T | C | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(35): Show |
215 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*405A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12313 | chr4 | 100398008 | ||||||
| chr4:100398009 | G | A | 1 | a0002c0002t0016 | 2 | HG02922.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*404C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12312 | chr4 | 100398009 | ||||||
| chr4:100398044 | T | C | 1 | a0002c0002t0016 | 2 | HG02922.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*369A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12277 | chr4 | 100398044 | ||||||
| chr4:100398051 | G | A | 1 | a0001c0001t0032 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*362C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12270 | chr4 | 100398051 | ||||||
| chr4:100398130 | T | A | 1 | a0004c0005t0017 | 2 | HG00735.hp1 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*283A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12191 | chr4 | 100398130 | ||||||
| chr4:100398137 | C | T | 1 | a0001c0001t0008 | 5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*276G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12184 | chr4 | 100398137 | ||||||
| chr4:100398170 | A | G | 3 | a0001c0001t0007 a0001c0001t0008 a0002c0002t0007 |
15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*243T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12151 | chr4 | 100398170 | ||||||
| chr4:100398175 | G | A | 5 | a0001c0001t0006 a0001c0001t0033 a0001c0001t0034 others(2): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*238C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12146 | chr4 | 100398175 | ||||||
| chr4:100398242 | T | C | 1 | a0003c0003t0035 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*171A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12079 | chr4 | 100398242 | ||||||
| chr4:100398298 | A | G | 1 | a0002c0002t0014 | 2 | NA18980.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*115T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 12023 | chr4 | 100398298 | ||||||
| chr4:100398345 | G | A | 1 | a0003c0003t0036 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*68C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 12/12 | 11976 | chr4 | 100398345 | ||||||
| chr4:100410300 | T | C | 1 | a0001c0001t0038 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/12 | 21 | chr4 | 100410300 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:100398380 | G | GCAA | 64 | a0001c0001t0002g0003 a0001c0001t0002g0122 a0001c0001t0002g0127 others(61): Show |
65 | HG00673.hp2 HG00735.hp2 HG00738.hp2 others(62): Show |
splice_region_variant&intron_variant | LOW | c.*40-10_*40-8dupTTG | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100398380 | |||||||
| chr4:100398380 | G | GCAACAA | 3 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0225 |
3 | HG00597.hp1 HG02027.hp2 HG02132.hp1 |
splice_region_variant&intron_variant | LOW | c.*40-13_*40-8dupTTG others(3): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100398380 | |||||||
| chr4:100398516 | A | G | 80 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(77): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*40-143T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100398516 | |||||||
| chr4:100398629 | T | C | 11 | a0001c0001t0008g0116 a0001c0001t0008g0117 a0001c0001t0008g0118 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.*40-256A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100398629 | |||||||
| chr4:100398692 | C | T | 16 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(13): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.*40-319G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100398692 | |||||||
| chr4:100398714 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.*40-341T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100398714 | |||||||
| chr4:100398792 | A | G | 19 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(16): Show |
20 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.*40-419T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100398792 | |||||||
| chr4:100399124 | C | G | 5 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(2): Show |
5 | HG02486.hp2 HG02896.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.*40-751G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399124 | |||||||
| chr4:100399127 | C | T | 1 | a0002c0002t0001g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.*40-754G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399127 | |||||||
| chr4:100399195 | C | T | 1 | a0001c0001t0032g0254 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.*40-822G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399195 | |||||||
| chr4:100399255 | T | C | 227 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(224): Show |
231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.*40-882A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399255 | |||||||
| chr4:100399381 | G | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*40-1008C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399381 | |||||||
| chr4:100399421 | G | C | 1 | a0001c0001t0003g0212 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.*40-1048C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399421 | |||||||
| chr4:100399585 | G | A | 2 | a0002c0002t0001g0056 a0002c0002t0001g0064 |
2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.*40-1212C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399585 | |||||||
| chr4:100399649 | A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*40-1276T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399649 | |||||||
| chr4:100399680 | C | T | 210 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(207): Show |
214 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.*40-1307G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399680 | |||||||
| chr4:100399836 | G | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*40-1463C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399836 | |||||||
| chr4:100399855 | G | A | 7 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(4): Show |
8 | HG01109.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.*40-1482C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399855 | |||||||
| chr4:100399885 | T | C | 21 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(18): Show |
21 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.*40-1512A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399885 | |||||||
| chr4:100399941 | T | C | 1 | a0001c0001t0002g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.*40-1568A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100399941 | |||||||
| chr4:100400043 | T | C | 211 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(208): Show |
215 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(212): Show |
intron_variant | MODIFIER | c.*40-1670A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400043 | |||||||
| chr4:100400066 | G | A | 15 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.*40-1693C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400066 | |||||||
| chr4:100400224 | C | T | 1 | a0002c0002t0016g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.*40-1851G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400224 | |||||||
| chr4:100400238 | A | C | 1 | a0001c0001t0004g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*40-1865T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400238 | |||||||
| chr4:100400285 | AT | A | 16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.*40-1913delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400285 | |||||||
| chr4:100400353 | A | AT | 54 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(51): Show |
55 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.*40-1981dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400353 | |||||||
| chr4:100400353 | AT | A | 98 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(95): Show |
99 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.*40-1981delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400353 | |||||||
| chr4:100400360 | T | G | 59 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(56): Show |
60 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.*40-1987A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400360 | |||||||
| chr4:100400442 | T | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*40-2069A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400442 | |||||||
| chr4:100400498 | T | C | 80 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(77): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*40-2125A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400498 | |||||||
| chr4:100400607 | C | T | 211 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(208): Show |
215 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(212): Show |
intron_variant | MODIFIER | c.*40-2234G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400607 | |||||||
| chr4:100400745 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0185 a0002c0002t0001g0075 |
3 | HG00408.hp2 NA19012.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.*40-2372T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400745 | |||||||
| chr4:100400944 | T | C | 102 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(99): Show |
103 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.*40-2571A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100400944 | |||||||
| chr4:100401139 | G | T | 80 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(77): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*40-2766C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401139 | |||||||
| chr4:100401146 | G | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*40-2773C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401146 | |||||||
| chr4:100401521 | G | C | 1 | a0001c0001t0002g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.*40-3148C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401521 | |||||||
| chr4:100401528 | T | C | 3 | a0002c0002t0016g0110 a0002c0002t0016g0111 a0003c0003t0035g0198 |
3 | HG02896.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*40-3155A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401528 | |||||||
| chr4:100401663 | A | T | 211 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(208): Show |
215 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(212): Show |
intron_variant | MODIFIER | c.*40-3290T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401663 | |||||||
| chr4:100401720 | C | A | 80 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(77): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*40-3347G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401720 | |||||||
| chr4:100401775 | T | C | 3 | a0002c0002t0001g0042 a0002c0002t0001g0070 a0002c0002t0001g0108 |
3 | HG01261.hp2 HG02148.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.*40-3402A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401775 | |||||||
| chr4:100401846 | G | T | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.*40-3473C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401846 | |||||||
| chr4:100401974 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.*40-3601G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100401974 | |||||||
| chr4:100402055 | C | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*40-3682G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402055 | |||||||
| chr4:100402099 | A | T | 1 | a0002c0002t0025g0059 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.*40-3726T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402099 | |||||||
| chr4:100402116 | G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*40-3743C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402116 | |||||||
| chr4:100402185 | A | C | 1 | a0002c0002t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*40-3812T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402185 | |||||||
| chr4:100402214 | C | G | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*40-3841G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402214 | |||||||
| chr4:100402223 | C | G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.*40-3850G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402223 | |||||||
| chr4:100402252 | T | G | 139 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(136): Show |
141 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.*40-3879A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402252 | |||||||
| chr4:100402655 | A | C | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.*40-4282T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402655 | |||||||
| chr4:100402767 | G | C | 1 | a0002c0002t0001g0098 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.*40-4394C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402767 | |||||||
| chr4:100402771 | C | T | 23 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(20): Show |
23 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.*40-4398G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402771 | |||||||
| chr4:100402772 | G | A | 15 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.*40-4399C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402772 | |||||||
| chr4:100402972 | A | G | 15 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.*40-4599T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402972 | |||||||
| chr4:100402972 | A | T | 43 | a0001c0001t0002g0003 a0001c0001t0002g0122 a0001c0001t0002g0127 others(40): Show |
44 | HG00597.hp1 HG00673.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.*40-4599T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100402972 | |||||||
| chr4:100403012 | C | G | 3 | a0001c0001t0004g0154 a0001c0001t0004g0156 a0001c0001t0019g0155 |
3 | HG02145.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.*40-4639G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403012 | |||||||
| chr4:100403157 | G | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*40-4784C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403157 | |||||||
| chr4:100403243 | C | T | 3 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0026g0049 |
3 | HG02451.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*40-4870G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403243 | |||||||
| chr4:100403256 | T | C | 104 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(101): Show |
105 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.*40-4883A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403256 | |||||||
| chr4:100403257 | A | G | 5 | a0002c0002t0001g0046 a0002c0002t0001g0054 a0002c0002t0001g0055 others(2): Show |
5 | HG01346.hp1 HG01934.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.*40-4884T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403257 | |||||||
| chr4:100403282 | C | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*40-4909G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403282 | |||||||
| chr4:100403414 | C | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*40-5041G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403414 | |||||||
| chr4:100403447 | A | ATGGGCAT others(9): Show |
22 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(19): Show |
22 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.*40-5090_*40-5075d others(18): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403447 | |||||||
| chr4:100403447 | A | ATGGGCAT others(25): Show |
1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*40-5106_*40-5075d others(34): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403447 | |||||||
| chr4:100403447 | ATGGGCAT others(9): Show |
A | 80 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(77): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*40-5090_*40-5075d others(18): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403447 | |||||||
| chr4:100403543 | C | T | 72 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0007 others(69): Show |
74 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.*40-5170G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403543 | |||||||
| chr4:100403650 | G | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*40-5277C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403650 | |||||||
| chr4:100403721 | C | T | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*40-5348G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403721 | |||||||
| chr4:100403748 | T | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.*40-5375A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403748 | |||||||
| chr4:100403779 | G | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*40-5406C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100403779 | |||||||
| chr4:100404021 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.*40-5648C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404021 | |||||||
| chr4:100404119 | T | A | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*40-5746A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404119 | |||||||
| chr4:100404242 | G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*40-5869C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404242 | |||||||
| chr4:100404355 | G | C | 1 | a0002c0002t0037g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.*39+5927C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404355 | |||||||
| chr4:100404476 | A | G | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.*39+5806T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404476 | |||||||
| chr4:100404487 | G | A | 16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.*39+5795C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404487 | |||||||
| chr4:100404500 | T | C | 4 | a0001c0001t0005g0183 a0001c0001t0005g0191 a0001c0001t0005g0192 others(1): Show |
4 | HG02615.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.*39+5782A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404500 | |||||||
| chr4:100404606 | T | C | 1 | a0001c0001t0002g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*39+5676A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404606 | |||||||
| chr4:100404663 | C | A | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.*39+5619G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100404663 | |||||||
| chr4:100405145 | A | T | 124 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(121): Show |
126 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.*39+5137T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405145 | |||||||
| chr4:100405163 | C | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*39+5119G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405163 | |||||||
| chr4:100405173 | A | G | 227 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(224): Show |
231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.*39+5109T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405173 | |||||||
| chr4:100405234 | T | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*39+5048A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405234 | |||||||
| chr4:100405371 | T | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*39+4911A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405371 | |||||||
| chr4:100405758 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*39+4524C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405758 | |||||||
| chr4:100405874 | G | GT | 7 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(4): Show |
8 | HG01109.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.*39+4407dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405874 | |||||||
| chr4:100405913 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.*39+4369C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405913 | |||||||
| chr4:100405949 | T | C | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*39+4333A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100405949 | |||||||
| chr4:100406146 | C | A | 1 | a0002c0002t0007g0168 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*39+4136G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100406146 | |||||||
| chr4:100406508 | A | G | 6 | a0002c0002t0001g0086 a0002c0002t0001g0087 a0002c0002t0001g0091 others(3): Show |
6 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.*39+3774T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100406508 | |||||||
| chr4:100406521 | A | T | 15 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.*39+3761T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100406521 | |||||||
| chr4:100406545 | T | A | 16 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(13): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.*39+3737A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100406545 | |||||||
| chr4:100406591 | G | A | 19 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(16): Show |
19 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.*39+3691C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100406591 | |||||||
| chr4:100406591 | G | T | 81 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(78): Show |
82 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.*39+3691C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100406591 | |||||||
| chr4:100407287 | G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*39+2995C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407287 | |||||||
| chr4:100407314 | A | G | 83 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(80): Show |
84 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.*39+2968T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407314 | |||||||
| chr4:100407478 | A | G | 238 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(235): Show |
242 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(239): Show |
intron_variant | MODIFIER | c.*39+2804T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407478 | |||||||
| chr4:100407491 | C | T | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*39+2791G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407491 | |||||||
| chr4:100407502 | A | G | 80 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(77): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*39+2780T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407502 | |||||||
| chr4:100407568 | A | G | 6 | a0002c0002t0007g0163 a0002c0002t0007g0164 a0002c0002t0007g0165 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.*39+2714T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407568 | |||||||
| chr4:100407606 | T | G | 227 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(224): Show |
231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.*39+2676A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407606 | |||||||
| chr4:100407631 | T | C | 3 | a0002c0002t0016g0110 a0002c0002t0016g0111 a0003c0003t0035g0198 |
3 | HG02896.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*39+2651A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407631 | |||||||
| chr4:100407772 | C | T | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 |
3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.*39+2510G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407772 | |||||||
| chr4:100407909 | A | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*39+2373T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100407909 | |||||||
| chr4:100408001 | C | T | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.*39+2281G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408001 | |||||||
| chr4:100408017 | G | A | 5 | a0001c0001t0009g0121 a0001c0001t0009g0153 a0001c0001t0009g0242 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.*39+2265C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408017 | |||||||
| chr4:100408096 | T | C | 3 | a0002c0002t0016g0110 a0002c0002t0016g0111 a0003c0003t0035g0198 |
3 | HG02896.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*39+2186A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408096 | |||||||
| chr4:100408147 | C | T | 1 | a0001c0001t0002g0012 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.*39+2135G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408147 | |||||||
| chr4:100408151 | G | A | 80 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(77): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*39+2131C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408151 | |||||||
| chr4:100408175 | T | C | 83 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(80): Show |
84 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.*39+2107A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408175 | |||||||
| chr4:100408284 | A | C | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*39+1998T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408284 | |||||||
| chr4:100408392 | G | A | 1 | a0001c0004t0004g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.*39+1890C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408392 | |||||||
| chr4:100408617 | T | C | 227 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(224): Show |
231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.*39+1665A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408617 | |||||||
| chr4:100408633 | A | G | 3 | a0002c0002t0016g0110 a0002c0002t0016g0111 a0003c0003t0035g0198 |
3 | HG02896.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*39+1649T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408633 | |||||||
| chr4:100408655 | T | C | 1 | a0001c0001t0006g0006 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.*39+1627A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408655 | |||||||
| chr4:100408729 | T | C | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*39+1553A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408729 | |||||||
| chr4:100408782 | C | T | 80 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(77): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*39+1500G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408782 | |||||||
| chr4:100408788 | C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*39+1494G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408788 | |||||||
| chr4:100408832 | C | T | 29 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(26): Show |
30 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.*39+1450G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408832 | |||||||
| chr4:100408844 | A | G | 83 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(80): Show |
84 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.*39+1438T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408844 | |||||||
| chr4:100408853 | T | A | 72 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0007 others(69): Show |
74 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.*39+1429A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408853 | |||||||
| chr4:100408865 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.*39+1417T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408865 | |||||||
| chr4:100408896 | C | G | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*39+1386G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408896 | |||||||
| chr4:100408904 | T | C | 2 | a0002c0002t0001g0065 a0002c0002t0001g0081 |
2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.*39+1378A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100408904 | |||||||
| chr4:100409159 | C | T | 5 | a0001c0001t0009g0121 a0001c0001t0009g0153 a0001c0001t0009g0242 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.*39+1123G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409159 | |||||||
| chr4:100409215 | A | ATTTAT | 81 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(78): Show |
82 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.*39+1062_*39+1066d others(7): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409215 | |||||||
| chr4:100409215 | A | ATTTATTT others(3): Show |
1 | a0002c0002t0026g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.*39+1066_*39+1067i others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409215 | |||||||
| chr4:100409215 | A | ATTTATTT others(3): Show |
1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*39+1057_*39+1066d others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409215 | |||||||
| chr4:100409242 | T | G | 3 | a0002c0002t0016g0110 a0002c0002t0016g0111 a0003c0003t0035g0198 |
3 | HG02896.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*39+1040A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409242 | |||||||
| chr4:100409303 | C | T | 16 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(13): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.*39+979G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409303 | |||||||
| chr4:100409320 | T | G | 80 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(77): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*39+962A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409320 | |||||||
| chr4:100409345 | A | G | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.*39+937T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409345 | |||||||
| chr4:100409380 | A | C | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.*39+902T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409380 | |||||||
| chr4:100409395 | C | G | 15 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.*39+887G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409395 | |||||||
| chr4:100409429 | C | T | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*39+853G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409429 | |||||||
| chr4:100409430 | G | A | 29 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(26): Show |
30 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.*39+852C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409430 | |||||||
| chr4:100409588 | G | A | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.*39+694C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409588 | |||||||
| chr4:100409599 | T | C | 124 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(121): Show |
126 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.*39+683A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409599 | |||||||
| chr4:100409820 | T | C | 4 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(1): Show |
4 | HG01975.hp1 HG02922.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.*39+462A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409820 | |||||||
| chr4:100409826 | A | G | 1 | a0001c0001t0003g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.*39+456T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409826 | |||||||
| chr4:100409914 | G | A | 1 | a0005c0007t0002g0209 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.*39+368C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100409914 | |||||||
| chr4:100410102 | C | A | 3 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 |
3 | HG01975.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*39+180G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100410102 | |||||||
| chr4:100410131 | T | C | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.*39+151A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100410131 | |||||||
| chr4:100410186 | C | T | 106 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(103): Show |
107 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.*39+96G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100410186 | |||||||
| chr4:100410218 | G | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*39+64C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 11/11 | chr4 | 100410218 | |||||||
| chr4:100410489 | G | A | 1 | a0001c0001t0005g0191 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.752-134C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410489 | |||||||
| chr4:100410606 | T | C | 25 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(22): Show |
25 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(22): Show |
intron_variant | MODIFIER | c.752-251A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410606 | |||||||
| chr4:100410613 | G | A | 2 | a0001c0001t0009g0121 a0001c0001t0009g0153 |
2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.752-258C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410613 | |||||||
| chr4:100410697 | C | T | 1 | a0002c0002t0001g0135 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.752-342G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410697 | |||||||
| chr4:100410711 | T | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.752-356A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410711 | |||||||
| chr4:100410716 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.752-361A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410716 | |||||||
| chr4:100410719 | G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.752-364C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410719 | |||||||
| chr4:100410757 | C | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.752-402G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100410757 | |||||||
| chr4:100411154 | C | T | 1 | a0001c0001t0002g0007 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.752-799G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411154 | |||||||
| chr4:100411160 | C | T | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.752-805G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411160 | |||||||
| chr4:100411230 | G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.752-875C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411230 | |||||||
| chr4:100411259 | A | C | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.752-904T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411259 | |||||||
| chr4:100411314 | C | T | 1 | a0002c0002t0016g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.752-959G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411314 | |||||||
| chr4:100411333 | C | T | 2 | a0001c0001t0020g0023 a0003c0003t0004g0158 |
2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.752-978G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411333 | |||||||
| chr4:100411350 | C | T | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.752-995G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411350 | |||||||
| chr4:100411395 | G | T | 104 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(101): Show |
105 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.752-1040C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411395 | |||||||
| chr4:100411429 | G | A | 3 | a0002c0002t0007g0166 a0002c0002t0007g0167 a0002c0002t0007g0168 |
3 | HG02717.hp2 HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.752-1074C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411429 | |||||||
| chr4:100411456 | G | T | 227 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(224): Show |
231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.752-1101C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411456 | |||||||
| chr4:100411601 | A | G | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.752-1246T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411601 | |||||||
| chr4:100411643 | T | C | 72 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0007 others(69): Show |
74 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.752-1288A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411643 | |||||||
| chr4:100411678 | C | A | 1 | a0002c0002t0006g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.752-1323G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411678 | |||||||
| chr4:100411754 | T | A | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.752-1399A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411754 | |||||||
| chr4:100411775 | T | C | 23 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(20): Show |
23 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.752-1420A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411775 | |||||||
| chr4:100411800 | A | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.752-1445T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411800 | |||||||
| chr4:100411876 | C | T | 2 | a0001c0001t0006g0142 a0001c0001t0006g0143 |
2 | HG00639.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.752-1521G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411876 | |||||||
| chr4:100411883 | C | T | 7 | a0001c0001t0029g0159 a0002c0002t0007g0163 a0002c0002t0007g0164 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.752-1528G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411883 | |||||||
| chr4:100411937 | T | C | 1 | a0001c0001t0006g0157 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.752-1582A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411937 | |||||||
| chr4:100411952 | T | TC | 3 | a0002c0002t0016g0110 a0002c0002t0016g0111 a0003c0003t0035g0198 |
3 | HG02896.hp1 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.752-1598_752-1597i others(3): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411952 | |||||||
| chr4:100411970 | A | G | 1 | a0001c0001t0006g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.752-1615T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100411970 | |||||||
| chr4:100412011 | A | G | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.752-1656T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412011 | |||||||
| chr4:100412044 | ATTAG | A | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.752-1693_752-1690d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412044 | |||||||
| chr4:100412051 | AGTTT | A | 3 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0225 |
3 | HG00597.hp1 HG02027.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.752-1700_752-1697d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412051 | |||||||
| chr4:100412172 | A | G | 6 | a0002c0002t0007g0163 a0002c0002t0007g0164 a0002c0002t0007g0165 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.752-1817T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412172 | |||||||
| chr4:100412201 | G | A | 29 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(26): Show |
30 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.752-1846C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412201 | |||||||
| chr4:100412274 | G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.752-1919C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412274 | |||||||
| chr4:100412309 | C | T | 80 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(77): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.752-1954G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412309 | |||||||
| chr4:100412625 | C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.752-2270G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412625 | |||||||
| chr4:100412798 | A | G | 80 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(77): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.752-2443T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412798 | |||||||
| chr4:100412836 | A | C | 108 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(105): Show |
109 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.752-2481T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412836 | |||||||
| chr4:100412845 | T | C | 16 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(13): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.752-2490A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412845 | |||||||
| chr4:100412849 | T | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.752-2494A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412849 | |||||||
| chr4:100412904 | T | TG | 139 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(136): Show |
141 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.752-2550dupC | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412904 | |||||||
| chr4:100412965 | G | A | 1 | a0001c0001t0020g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.752-2610C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412965 | |||||||
| chr4:100412995 | C | A | 232 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(229): Show |
236 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(233): Show |
intron_variant | MODIFIER | c.752-2640G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100412995 | |||||||
| chr4:100413113 | A | G | 7 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(4): Show |
8 | HG01109.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.752-2758T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413113 | |||||||
| chr4:100413296 | A | T | 1 | a0002c0002t0001g0094 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.751+2602T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413296 | |||||||
| chr4:100413298 | A | G | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.751+2600T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413298 | |||||||
| chr4:100413565 | T | G | 1 | a0002c0002t0001g0237 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.751+2333A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413565 | |||||||
| chr4:100413612 | G | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.751+2286C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413612 | |||||||
| chr4:100413704 | A | G | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.751+2194T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413704 | |||||||
| chr4:100413707 | G | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.751+2191C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413707 | |||||||
| chr4:100413801 | A | G | 43 | a0001c0001t0002g0003 a0001c0001t0002g0122 a0001c0001t0002g0127 others(40): Show |
44 | HG00597.hp1 HG00673.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.751+2097T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413801 | |||||||
| chr4:100413843 | A | C | 5 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0001g0097 others(2): Show |
5 | HG00597.hp2 HG01361.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.751+2055T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413843 | |||||||
| chr4:100413919 | C | T | 2 | a0001c0001t0002g0187 a0001c0001t0002g0217 |
2 | HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.751+1979G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100413919 | |||||||
| chr4:100414086 | G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.751+1812C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414086 | |||||||
| chr4:100414228 | G | A | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.751+1670C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414228 | |||||||
| chr4:100414348 | C | CT | 53 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0011 others(50): Show |
55 | HG00639.hp1 HG00639.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.751+1549dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414348 | |||||||
| chr4:100414348 | C | CTT | 16 | a0001c0001t0002g0184 a0001c0001t0002g0232 a0001c0001t0004g0018 others(13): Show |
16 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.751+1548_751+1549d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414348 | |||||||
| chr4:100414348 | CT | C | 16 | a0001c0001t0002g0012 a0001c0001t0002g0040 a0001c0001t0003g0235 others(13): Show |
16 | HG01069.hp2 HG01070.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.751+1549delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414348 | |||||||
| chr4:100414348 | CTTTTTTT others(2): Show |
C | 77 | a0001c0001t0001g0043 a0001c0001t0001g0101 a0001c0001t0001g0182 others(74): Show |
78 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.751+1541_751+1549d others(11): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414348 | |||||||
| chr4:100414348 | CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0001g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.751+1540_751+1549d others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414348 | |||||||
| chr4:100414348 | CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0037g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.751+1538_751+1549d others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414348 | |||||||
| chr4:100414348 | CTTTTTTT others(7): Show |
C | 6 | a0002c0002t0007g0163 a0002c0002t0007g0164 a0002c0002t0007g0165 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.751+1536_751+1549d others(16): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414348 | |||||||
| chr4:100414381 | C | T | 2 | a0001c0001t0028g0175 a0003c0003t0036g0160 |
2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.751+1517G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414381 | |||||||
| chr4:100414563 | G | A | 80 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(77): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.751+1335C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414563 | |||||||
| chr4:100414653 | C | T | 227 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(224): Show |
231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.751+1245G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414653 | |||||||
| chr4:100414720 | A | T | 74 | a0001c0001t0001g0043 a0001c0001t0001g0101 a0001c0001t0001g0182 others(71): Show |
75 | HG00408.hp1 HG00597.hp2 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.751+1178T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414720 | |||||||
| chr4:100414931 | C | A | 1 | a0002c0002t0007g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.751+967G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414931 | |||||||
| chr4:100414931 | C | T | 20 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(17): Show |
21 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.751+967G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414931 | |||||||
| chr4:100414952 | G | C | 72 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0007 others(69): Show |
74 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.751+946C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414952 | |||||||
| chr4:100414960 | G | A | 23 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(20): Show |
23 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.751+938C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414960 | |||||||
| chr4:100414988 | C | G | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.751+910G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414988 | |||||||
| chr4:100414988 | C | T | 23 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(20): Show |
23 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.751+910G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414988 | |||||||
| chr4:100414999 | A | G | 1 | a0001c0001t0023g0005 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.751+899T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100414999 | |||||||
| chr4:100415210 | A | C | 3 | a0001c0001t0003g0218 a0001c0001t0003g0220 a0002c0002t0003g0047 |
3 | HG01074.hp2 HG01934.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.751+688T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415210 | |||||||
| chr4:100415228 | T | C | 1 | a0001c0001t0003g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.751+670A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415228 | |||||||
| chr4:100415243 | G | A | 80 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(77): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.751+655C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415243 | |||||||
| chr4:100415264 | T | A | 1 | a0001c0001t0003g0102 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.751+634A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415264 | |||||||
| chr4:100415366 | T | C | 1 | a0001c0001t0002g0193 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.751+532A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415366 | |||||||
| chr4:100415481 | T | C | 1 | a0001c0001t0008g0120 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.751+417A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415481 | |||||||
| chr4:100415660 | A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.751+238T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415660 | |||||||
| chr4:100415681 | T | C | 2 | a0001c0001t0002g0014 a0001c0001t0002g0015 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.751+217A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415681 | |||||||
| chr4:100415730 | G | A | 23 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(20): Show |
23 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.751+168C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415730 | |||||||
| chr4:100415792 | A | G | 1 | a0002c0002t0001g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.751+106T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 10/11 | chr4 | 100415792 | |||||||
| chr4:100415973 | A | T | 16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.690-14T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100415973 | |||||||
| chr4:100415976 | A | C | 3 | a0001c0001t0003g0235 a0001c0001t0003g0258 a0001c0001t0018g0219 |
3 | HG00642.hp1 HG02602.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.690-17T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100415976 | |||||||
| chr4:100415986 | A | G | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | NA18979.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.690-27T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100415986 | |||||||
| chr4:100415993 | C | T | 42 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(39): Show |
43 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.690-34G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100415993 | |||||||
| chr4:100416058 | C | CAT | 5 | a0001c0004t0004g0248 a0001c0004t0004g0249 a0002c0002t0016g0110 others(2): Show |
5 | HG02257.hp2 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.690-101_690-100dup others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416058 | |||||||
| chr4:100416091 | C | CAT | 21 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(18): Show |
21 | HG01070.hp2 HG01884.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.690-133_690-132ins others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416091 | |||||||
| chr4:100416091 | C | CGT | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-134_690-133dup others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416091 | |||||||
| chr4:100416113 | C | CAT | 19 | a0001c0001t0002g0187 a0001c0001t0002g0203 a0001c0001t0002g0217 others(16): Show |
19 | HG00639.hp1 HG00673.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.690-156_690-155dup others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416113 | |||||||
| chr4:100416130 | A | C | 2 | a0001c0001t0002g0221 a0001c0001t0002g0226 |
2 | HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.690-171T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416130 | |||||||
| chr4:100416148 | T | C | 1 | a0001c0001t0003g0103 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.690-189A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416148 | |||||||
| chr4:100416229 | T | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.690-270A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416229 | |||||||
| chr4:100416280 | G | T | 6 | a0001c0001t0004g0154 a0001c0001t0004g0156 a0001c0001t0019g0155 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.690-321C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416280 | |||||||
| chr4:100416373 | G | T | 227 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(224): Show |
231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.690-414C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416373 | |||||||
| chr4:100416492 | T | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.690-533A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416492 | |||||||
| chr4:100416554 | G | A | 16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.689+563C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416554 | |||||||
| chr4:100416777 | A | G | 5 | a0001c0001t0009g0121 a0001c0001t0009g0153 a0001c0001t0009g0242 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.689+340T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416777 | |||||||
| chr4:100416870 | A | C | 80 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(77): Show |
81 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.689+247T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416870 | |||||||
| chr4:100416903 | A | T | 1 | a0001c0001t0002g0229 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.689+214T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416903 | |||||||
| chr4:100416949 | A | G | 3 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 |
4 | HG01257.hp2 HG01258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+168T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100416949 | |||||||
| chr4:100417035 | CA | C | 35 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(32): Show |
35 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.689+81delT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100417035 | |||||||
| chr4:100417060 | T | C | 72 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0007 others(69): Show |
74 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.689+57A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 9/11 | chr4 | 100417060 | |||||||
| chr4:100417378 | G | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.665-237C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417378 | |||||||
| chr4:100417476 | T | C | 2 | a0001c0001t0011g0112 a0001c0001t0011g0114 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.665-335A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417476 | |||||||
| chr4:100417577 | GTGTTTGT others(12): Show |
G | 5 | a0001c0001t0008g0116 a0001c0001t0008g0117 a0001c0001t0008g0118 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.665-455_665-437del others(19): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417577 | |||||||
| chr4:100417658 | C | T | 1 | a0002c0002t0010g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.665-517G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417658 | |||||||
| chr4:100417741 | C | G | 1 | a0002c0002t0001g0150 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.665-600G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417741 | |||||||
| chr4:100417756 | A | C | 1 | a0001c0001t0002g0011 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.665-615T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417756 | |||||||
| chr4:100417781 | C | T | 119 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(116): Show |
120 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.665-640G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417781 | |||||||
| chr4:100417842 | A | G | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.665-701T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417842 | |||||||
| chr4:100417944 | T | G | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.665-803A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417944 | |||||||
| chr4:100417952 | C | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.665-811G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417952 | |||||||
| chr4:100417977 | T | C | 2 | a0001c0001t0003g0186 a0001c0001t0003g0188 |
2 | HG01258.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.665-836A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100417977 | |||||||
| chr4:100418078 | AT | A | 227 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(224): Show |
231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.665-938delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100418078 | |||||||
| chr4:100418153 | A | G | 1 | a0001c0001t0002g0228 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.665-1012T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100418153 | |||||||
| chr4:100418590 | A | G | 4 | a0002c0002t0001g0046 a0002c0002t0001g0071 a0002c0002t0001g0074 others(1): Show |
4 | HG01255.hp1 HG01346.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.665-1449T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100418590 | |||||||
| chr4:100418825 | A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.665-1684T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100418825 | |||||||
| chr4:100418913 | G | T | 7 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(4): Show |
8 | HG01109.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.665-1772C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100418913 | |||||||
| chr4:100419012 | C | T | 207 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(204): Show |
210 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(207): Show |
intron_variant | MODIFIER | c.665-1871G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419012 | |||||||
| chr4:100419016 | C | T | 16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.665-1875G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419016 | |||||||
| chr4:100419096 | G | A | 16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.665-1955C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419096 | |||||||
| chr4:100419097 | G | A | 3 | a0001c0001t0002g0187 a0001c0001t0002g0203 a0001c0001t0002g0217 |
3 | HG00738.hp2 HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.665-1956C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419097 | |||||||
| chr4:100419226 | G | A | 16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.664+2056C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419226 | |||||||
| chr4:100419360 | G | A | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.664+1922C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419360 | |||||||
| chr4:100419506 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.664+1776C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419506 | |||||||
| chr4:100419539 | A | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.664+1743T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419539 | |||||||
| chr4:100419571 | T | G | 15 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.664+1711A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419571 | |||||||
| chr4:100419611 | T | A | 16 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(13): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.664+1671A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419611 | |||||||
| chr4:100419627 | T | A | 207 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(204): Show |
210 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(207): Show |
intron_variant | MODIFIER | c.664+1655A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419627 | |||||||
| chr4:100419844 | T | C | 36 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(33): Show |
37 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.664+1438A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419844 | |||||||
| chr4:100419845 | G | A | 34 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(31): Show |
35 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.664+1437C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419845 | |||||||
| chr4:100419853 | C | T | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+1429G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419853 | |||||||
| chr4:100419952 | G | A | 36 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(33): Show |
37 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.664+1330C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419952 | |||||||
| chr4:100419956 | C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.664+1326G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100419956 | |||||||
| chr4:100420105 | C | A | 34 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(31): Show |
35 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.664+1177G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420105 | |||||||
| chr4:100420131 | A | G | 16 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(13): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.664+1151T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420131 | |||||||
| chr4:100420168 | G | A | 76 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(73): Show |
77 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.664+1114C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420168 | |||||||
| chr4:100420228 | A | G | 16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.664+1054T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420228 | |||||||
| chr4:100420280 | T | G | 1 | a0001c0001t0009g0242 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.664+1002A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420280 | |||||||
| chr4:100420334 | T | TA | 35 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(32): Show |
36 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.664+947dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420334 | |||||||
| chr4:100420345 | A | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.664+937T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420345 | |||||||
| chr4:100420478 | C | T | 1 | a0001c0001t0006g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.664+804G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420478 | |||||||
| chr4:100420483 | A | G | 70 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(67): Show |
72 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.664+799T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420483 | |||||||
| chr4:100420521 | C | A | 203 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(200): Show |
206 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(203): Show |
intron_variant | MODIFIER | c.664+761G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420521 | |||||||
| chr4:100420562 | T | A | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.664+720A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420562 | |||||||
| chr4:100420613 | C | T | 5 | a0001c0001t0009g0121 a0001c0001t0009g0153 a0001c0001t0009g0242 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.664+669G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420613 | |||||||
| chr4:100420672 | A | G | 16 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(13): Show |
17 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.664+610T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420672 | |||||||
| chr4:100420690 | A | G | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.664+592T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420690 | |||||||
| chr4:100420844 | G | A | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+438C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420844 | |||||||
| chr4:100420928 | C | T | 29 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(26): Show |
30 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.664+354G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100420928 | |||||||
| chr4:100421055 | G | T | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 |
3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.664+227C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100421055 | |||||||
| chr4:100421095 | G | A | 43 | a0001c0001t0002g0122 a0001c0001t0005g0173 a0001c0001t0005g0174 others(40): Show |
43 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.664+187C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 8/11 | chr4 | 100421095 | |||||||
| chr4:100421449 | C | A | 19 | a0001c0001t0002g0122 a0001c0001t0004g0004 a0001c0001t0004g0018 others(16): Show |
20 | HG00735.hp2 HG01109.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.569-72G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421449 | |||||||
| chr4:100421482 | T | C | 17 | a0001c0001t0002g0122 a0001c0001t0003g0207 a0001c0001t0003g0210 others(14): Show |
17 | HG00735.hp2 HG01975.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.569-105A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421482 | |||||||
| chr4:100421507 | G | A | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-130C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421507 | |||||||
| chr4:100421541 | G | A | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.569-164C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421541 | |||||||
| chr4:100421652 | G | A | 1 | a0001c0001t0009g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.569-275C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421652 | |||||||
| chr4:100421765 | G | T | 190 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(187): Show |
193 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(190): Show |
intron_variant | MODIFIER | c.569-388C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421765 | |||||||
| chr4:100421901 | G | T | 29 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(26): Show |
30 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.569-524C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421901 | |||||||
| chr4:100421929 | G | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.569-552C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421929 | |||||||
| chr4:100421961 | G | A | 15 | a0001c0001t0002g0021 a0001c0001t0002g0024 a0001c0001t0002g0025 others(12): Show |
15 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.569-584C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100421961 | |||||||
| chr4:100422004 | G | GCCTT | 4 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(1): Show |
4 | HG01975.hp1 HG02922.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.569-631_569-628dup others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422004 | |||||||
| chr4:100422004 | G | T | 18 | a0001c0001t0002g0122 a0001c0001t0003g0207 a0001c0001t0003g0210 others(15): Show |
18 | HG00735.hp2 HG02145.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.569-627C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422004 | |||||||
| chr4:100422060 | G | C | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.569-683C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422060 | |||||||
| chr4:100422260 | G | C | 7 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(4): Show |
8 | HG01109.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+761C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422260 | |||||||
| chr4:100422749 | A | G | 2 | a0002c0002t0001g0086 a0002c0002t0001g0092 |
2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.568+272T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422749 | |||||||
| chr4:100422798 | T | A | 1 | a0001c0001t0005g0256 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.568+223A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422798 | |||||||
| chr4:100422801 | C | CTTTCTTT others(5): Show |
1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.568+219_568+220ins others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422801 | |||||||
| chr4:100422813 | C | T | 193 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(190): Show |
196 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(193): Show |
intron_variant | MODIFIER | c.568+208G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422813 | |||||||
| chr4:100422817 | C | CTTTCTTT others(4): Show |
16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.568+203_568+204ins others(11): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422817 | |||||||
| chr4:100422817 | C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.568+204G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422817 | |||||||
| chr4:100422822 | CT | C | 145 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(142): Show |
148 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.568+198delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422822 | |||||||
| chr4:100422822 | CTT | C | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.568+197_568+198del others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422822 | |||||||
| chr4:100422823 | T | TTTTC | 16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0133 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.568+197_568+198ins others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422823 | |||||||
| chr4:100422853 | T | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.568+168A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 7/11 | chr4 | 100422853 | |||||||
| chr4:100423128 | T | A | 1 | a0001c0001t0020g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.509-48A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 6/11 | chr4 | 100423128 | |||||||
| chr4:100423193 | G | A | 6 | a0002c0002t0001g0086 a0002c0002t0001g0087 a0002c0002t0001g0091 others(3): Show |
6 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.509-113C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 6/11 | chr4 | 100423193 | |||||||
| chr4:100423573 | C | A | 9 | a0001c0001t0003g0207 a0001c0001t0003g0210 a0001c0001t0003g0255 others(6): Show |
9 | HG02486.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.416-169G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100423573 | |||||||
| chr4:100423653 | G | A | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.416-249C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100423653 | |||||||
| chr4:100423724 | C | T | 17 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(14): Show |
17 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.416-320G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100423724 | |||||||
| chr4:100423730 | C | T | 29 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(26): Show |
30 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.416-326G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100423730 | |||||||
| chr4:100423971 | C | A | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.416-567G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100423971 | |||||||
| chr4:100423973 | A | G | 2 | a0002c0002t0014g0096 a0002c0002t0014g0137 |
2 | NA18980.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.416-569T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100423973 | |||||||
| chr4:100424016 | C | T | 2 | a0002c0002t0001g0060 a0002c0002t0025g0059 |
2 | NA18946.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.416-612G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424016 | |||||||
| chr4:100424127 | A | C | 1 | a0001c0001t0005g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.416-723T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424127 | |||||||
| chr4:100424137 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.416-733G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424137 | |||||||
| chr4:100424169 | ATAAT | A | 3 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 |
4 | HG01257.hp2 HG01258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-769_416-766del others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424169 | |||||||
| chr4:100424173 | T | C | 3 | a0001c0001t0004g0154 a0001c0001t0004g0156 a0001c0001t0019g0155 |
3 | HG02145.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.416-769A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424173 | |||||||
| chr4:100424277 | A | G | 2 | a0002c0002t0001g0016 a0002c0002t0001g0017 |
2 | NA18946.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.416-873T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424277 | |||||||
| chr4:100424308 | G | T | 45 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(42): Show |
46 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.416-904C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424308 | |||||||
| chr4:100424386 | G | C | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.416-982C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424386 | |||||||
| chr4:100424424 | A | G | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.416-1020T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424424 | |||||||
| chr4:100424454 | C | T | 1 | a0001c0001t0007g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.416-1050G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424454 | |||||||
| chr4:100424737 | A | G | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-1333T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424737 | |||||||
| chr4:100424897 | C | A | 1 | a0001c0001t0002g0003 | 2 | NA19001.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.416-1493G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424897 | |||||||
| chr4:100424965 | C | A | 1 | a0001c0001t0002g0194 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.416-1561G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100424965 | |||||||
| chr4:100425149 | G | GCACA | 47 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(44): Show |
48 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.416-1749_416-1746d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | |||||||
| chr4:100425149 | G | GCACACA | 26 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(23): Show |
27 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.416-1751_416-1746d others(8): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | |||||||
| chr4:100425149 | G | GCACACAC others(1): Show |
19 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0033 others(16): Show |
19 | HG00735.hp1 HG01070.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.416-1753_416-1746d others(10): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | |||||||
| chr4:100425149 | G | GCACACAC others(3): Show |
29 | a0001c0001t0002g0010 a0001c0001t0002g0236 a0001c0001t0004g0253 others(26): Show |
29 | HG00741.hp2 HG01099.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.416-1755_416-1746d others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | |||||||
| chr4:100425149 | G | GCACACAC others(5): Show |
73 | a0001c0001t0001g0043 a0001c0001t0001g0195 a0001c0001t0001g0196 others(70): Show |
75 | HG00408.hp1 HG00597.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.416-1757_416-1746d others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | |||||||
| chr4:100425149 | G | GCACACAC others(7): Show |
23 | a0001c0001t0001g0182 a0001c0001t0004g0154 a0001c0001t0004g0156 others(20): Show |
23 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.416-1759_416-1746d others(16): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | |||||||
| chr4:100425149 | G | GCACACAC others(9): Show |
5 | a0001c0001t0004g0018 a0001c0001t0004g0131 a0001c0001t0006g0134 others(2): Show |
5 | HG02132.hp2 HG02572.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-1761_416-1746d others(18): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | |||||||
| chr4:100425149 | G | GCACACAC others(11): Show |
2 | a0001c0001t0005g0189 a0001c0001t0006g0151 |
2 | HG02109.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.416-1763_416-1746d others(20): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425149 | |||||||
| chr4:100425203 | A | G | 3 | a0001c0001t0004g0154 a0001c0001t0004g0156 a0001c0001t0019g0155 |
3 | HG02145.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.416-1799T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425203 | |||||||
| chr4:100425234 | C | T | 2 | a0001c0001t0004g0251 a0001c0001t0004g0252 |
2 | HG01109.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.416-1830G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425234 | |||||||
| chr4:100425351 | GC | G | 194 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(191): Show |
197 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(194): Show |
intron_variant | MODIFIER | c.416-1948delG | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425351 | |||||||
| chr4:100425367 | A | C | 3 | a0001c0001t0003g0235 a0001c0001t0003g0258 a0001c0001t0018g0219 |
3 | HG00642.hp1 HG02602.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.416-1963T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425367 | |||||||
| chr4:100425390 | C | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.416-1986G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425390 | |||||||
| chr4:100425537 | C | T | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-2133G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425537 | |||||||
| chr4:100425655 | T | C | 26 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(23): Show |
27 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.416-2251A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425655 | |||||||
| chr4:100425984 | G | A | 83 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(80): Show |
84 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.416-2580C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100425984 | |||||||
| chr4:100426016 | A | G | 2 | a0001c0001t0002g0122 a0002c0002t0004g0162 |
2 | HG00735.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.416-2612T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426016 | |||||||
| chr4:100426035 | T | C | 2 | a0002c0002t0001g0060 a0002c0002t0025g0059 |
2 | NA18946.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.416-2631A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426035 | |||||||
| chr4:100426174 | T | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.416-2770A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426174 | |||||||
| chr4:100426242 | G | A | 3 | a0001c0001t0004g0154 a0001c0001t0004g0156 a0001c0001t0019g0155 |
3 | HG02145.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.416-2838C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426242 | |||||||
| chr4:100426337 | C | T | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.416-2933G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426337 | |||||||
| chr4:100426506 | C | G | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.416-3102G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426506 | |||||||
| chr4:100426584 | G | C | 42 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(39): Show |
43 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.416-3180C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426584 | |||||||
| chr4:100426588 | C | A | 9 | a0001c0001t0003g0207 a0001c0001t0003g0210 a0001c0001t0003g0255 others(6): Show |
9 | HG02486.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.416-3184G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426588 | |||||||
| chr4:100426938 | A | G | 1 | a0002c0002t0001g0144 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.416-3534T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100426938 | |||||||
| chr4:100427001 | T | A | 1 | a0002c0002t0001g0075 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.416-3597A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427001 | |||||||
| chr4:100427046 | G | C | 1 | a0001c0001t0002g0027 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.416-3642C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427046 | |||||||
| chr4:100427210 | T | A | 1 | a0002c0006t0004g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.416-3806A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427210 | |||||||
| chr4:100427255 | T | G | 35 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(32): Show |
35 | HG00639.hp1 HG00673.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.416-3851A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427255 | |||||||
| chr4:100427451 | C | CT | 7 | a0001c0001t0001g0196 a0001c0001t0008g0116 a0001c0001t0008g0117 others(4): Show |
7 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.416-4048dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427451 | |||||||
| chr4:100427452 | TC | T | 57 | a0001c0001t0002g0122 a0001c0001t0004g0004 a0001c0001t0004g0018 others(54): Show |
58 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.416-4049delG | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427452 | |||||||
| chr4:100427453 | C | T | 105 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(102): Show |
106 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.416-4049G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427453 | |||||||
| chr4:100427600 | T | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.416-4196A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427600 | |||||||
| chr4:100427767 | T | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.416-4363A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427767 | |||||||
| chr4:100427847 | C | G | 1 | a0001c0001t0027g0247 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.416-4443G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100427847 | |||||||
| chr4:100428063 | C | CAGCTGAC others(7): Show |
194 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(191): Show |
197 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(194): Show |
intron_variant | MODIFIER | c.416-4660_416-4659i others(16): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428063 | |||||||
| chr4:100428064 | C | G | 194 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(191): Show |
197 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(194): Show |
intron_variant | MODIFIER | c.416-4660G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428064 | |||||||
| chr4:100428115 | A | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.416-4711T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428115 | |||||||
| chr4:100428247 | C | T | 17 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(14): Show |
17 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.416-4843G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428247 | |||||||
| chr4:100428399 | C | T | 57 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(54): Show |
58 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.416-4995G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428399 | |||||||
| chr4:100428566 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.416-5162G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428566 | |||||||
| chr4:100428848 | G | A | 8 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0007g0163 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.416-5444C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428848 | |||||||
| chr4:100428969 | A | G | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-5565T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100428969 | |||||||
| chr4:100429026 | G | C | 1 | a0001c0001t0007g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.416-5622C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429026 | |||||||
| chr4:100429110 | C | T | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-5706G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429110 | |||||||
| chr4:100429147 | G | A | 2 | a0001c0001t0002g0122 a0002c0002t0004g0162 |
2 | HG00735.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.416-5743C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429147 | |||||||
| chr4:100429397 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.416-5993C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429397 | |||||||
| chr4:100429528 | C | T | 17 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(14): Show |
17 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.416-6124G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429528 | |||||||
| chr4:100429573 | G | T | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-6169C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429573 | |||||||
| chr4:100429722 | A | ATAG | 255 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(252): Show |
259 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(256): Show |
intron_variant | MODIFIER | c.416-6321_416-6319d others(5): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429722 | |||||||
| chr4:100429743 | A | C | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-6339T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429743 | |||||||
| chr4:100429792 | T | C | 4 | a0001c0001t0004g0004 a0001c0001t0004g0250 a0001c0001t0004g0251 others(1): Show |
5 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-6388A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429792 | |||||||
| chr4:100429801 | T | C | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.416-6397A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429801 | |||||||
| chr4:100429876 | T | G | 1 | a0001c0001t0002g0227 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.416-6472A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429876 | |||||||
| chr4:100429900 | C | T | 2 | a0004c0005t0017g0019 a0004c0005t0017g0020 |
2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.416-6496G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100429900 | |||||||
| chr4:100430240 | G | A | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.416-6836C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100430240 | |||||||
| chr4:100430259 | G | A | 1 | a0002c0002t0001g0057 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.416-6855C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100430259 | |||||||
| chr4:100430527 | A | G | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.416-7123T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100430527 | |||||||
| chr4:100430793 | G | A | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.416-7389C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100430793 | |||||||
| chr4:100430799 | A | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.416-7395T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100430799 | |||||||
| chr4:100430891 | A | G | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.416-7487T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100430891 | |||||||
| chr4:100430956 | A | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.416-7552T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100430956 | |||||||
| chr4:100431190 | C | A | 129 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(126): Show |
131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.416-7786G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431190 | |||||||
| chr4:100431212 | AAC | A | 3 | a0001c0001t0002g0184 a0001c0001t0002g0227 a0001c0001t0002g0232 |
3 | HG03831.hp1 HG03942.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.416-7810_416-7809d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431212 | |||||||
| chr4:100431243 | A | G | 1 | a0001c0001t0011g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.416-7839T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431243 | |||||||
| chr4:100431281 | A | G | 10 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(7): Show |
11 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.416-7877T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431281 | |||||||
| chr4:100431664 | G | A | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.416-8260C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431664 | |||||||
| chr4:100431694 | T | G | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-8290A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431694 | |||||||
| chr4:100431721 | A | ATC | 226 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(223): Show |
230 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(227): Show |
intron_variant | MODIFIER | c.416-8319_416-8318d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431721 | |||||||
| chr4:100431747 | CTGCTCTC others(11): Show |
C | 129 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(126): Show |
131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.416-8361_416-8344d others(20): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431747 | |||||||
| chr4:100431809 | C | T | 5 | a0001c0001t0009g0121 a0001c0001t0009g0153 a0001c0001t0009g0242 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-8405G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431809 | |||||||
| chr4:100431830 | G | A | 5 | a0001c0001t0009g0121 a0001c0001t0009g0153 a0001c0001t0009g0242 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-8426C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431830 | |||||||
| chr4:100431932 | G | C | 1 | a0001c0001t0033g0141 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.416-8528C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431932 | |||||||
| chr4:100431965 | G | A | 63 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(60): Show |
64 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.416-8561C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100431965 | |||||||
| chr4:100432017 | G | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.416-8613C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100432017 | |||||||
| chr4:100432080 | T | C | 1 | a0002c0002t0010g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.416-8676A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100432080 | |||||||
| chr4:100432144 | T | G | 1 | a0001c0001t0006g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.416-8740A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100432144 | |||||||
| chr4:100432163 | C | T | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-8759G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100432163 | |||||||
| chr4:100432383 | T | C | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.416-8979A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100432383 | |||||||
| chr4:100432426 | A | G | 129 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(126): Show |
131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.416-9022T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100432426 | |||||||
| chr4:100432679 | A | G | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-9275T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100432679 | |||||||
| chr4:100433306 | A | C | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.416-9902T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100433306 | |||||||
| chr4:100433543 | C | CT | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-10140dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100433543 | |||||||
| chr4:100433588 | T | C | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-10184A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100433588 | |||||||
| chr4:100433878 | G | A | 1 | a0002c0002t0010g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.416-10474C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100433878 | |||||||
| chr4:100433962 | A | G | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-10558T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100433962 | |||||||
| chr4:100433974 | C | T | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.416-10570G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100433974 | |||||||
| chr4:100434155 | T | C | 2 | a0001c0001t0038g0211 a0003c0003t0036g0160 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.416-10751A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434155 | |||||||
| chr4:100434271 | A | G | 94 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(91): Show |
95 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.416-10867T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434271 | |||||||
| chr4:100434378 | CCAAGCAA others(10): Show |
C | 129 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(126): Show |
131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.416-10991_416-1097 others(21): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434378 | |||||||
| chr4:100434383 | C | CA | 48 | a0001c0001t0002g0122 a0001c0001t0003g0186 a0001c0001t0003g0188 others(45): Show |
49 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.416-10980dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434383 | |||||||
| chr4:100434383 | C | CAA | 38 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(35): Show |
39 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.416-10981_416-1098 others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434383 | |||||||
| chr4:100434383 | C | CAAA | 5 | a0001c0001t0002g0181 a0001c0001t0002g0194 a0001c0001t0002g0233 others(2): Show |
5 | HG01192.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-10982_416-1098 others(7): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434383 | |||||||
| chr4:100434397 | A | G | 1 | a0001c0001t0020g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.416-10993T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434397 | |||||||
| chr4:100434424 | A | T | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-11020T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434424 | |||||||
| chr4:100434585 | C | T | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.416-11181G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434585 | |||||||
| chr4:100434644 | G | A | 1 | a0002c0002t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.416-11240C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434644 | |||||||
| chr4:100434660 | C | A | 41 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(38): Show |
42 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.416-11256G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434660 | |||||||
| chr4:100434689 | G | A | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.416-11285C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434689 | |||||||
| chr4:100434834 | G | A | 6 | a0001c0001t0005g0183 a0001c0001t0005g0191 a0001c0001t0005g0192 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-11430C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434834 | |||||||
| chr4:100434862 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.416-11458C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434862 | |||||||
| chr4:100434970 | C | A | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 |
3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.416-11566G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100434970 | |||||||
| chr4:100435034 | G | C | 1 | a0001c0001t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.416-11630C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435034 | |||||||
| chr4:100435143 | A | G | 2 | a0001c0001t0038g0211 a0003c0003t0036g0160 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.416-11739T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435143 | |||||||
| chr4:100435418 | A | G | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-12014T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435418 | |||||||
| chr4:100435431 | G | T | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-12027C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435431 | |||||||
| chr4:100435438 | T | C | 1 | a0001c0001t0002g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.416-12034A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435438 | |||||||
| chr4:100435442 | C | A | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-12038G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435442 | |||||||
| chr4:100435443 | A | T | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-12039T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435443 | |||||||
| chr4:100435730 | T | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.415+11803A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435730 | |||||||
| chr4:100435849 | C | T | 44 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(41): Show |
45 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.415+11684G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100435849 | |||||||
| chr4:100436174 | G | GA | 8 | a0001c0001t0005g0200 a0001c0001t0038g0211 a0002c0002t0016g0110 others(5): Show |
8 | HG00735.hp1 HG01070.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+11358dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436174 | |||||||
| chr4:100436178 | A | T | 129 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(126): Show |
131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.415+11355T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436178 | |||||||
| chr4:100436457 | T | C | 2 | a0004c0005t0017g0019 a0004c0005t0017g0020 |
2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.415+11076A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436457 | |||||||
| chr4:100436652 | A | G | 2 | a0001c0001t0002g0122 a0002c0002t0004g0162 |
2 | HG00735.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.415+10881T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436652 | |||||||
| chr4:100436751 | G | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.415+10782C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436751 | |||||||
| chr4:100436798 | C | T | 8 | a0002c0002t0001g0002 a0002c0002t0001g0042 a0002c0002t0001g0067 others(5): Show |
9 | HG01069.hp1 HG01071.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.415+10735G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436798 | |||||||
| chr4:100436850 | C | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.415+10683G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436850 | |||||||
| chr4:100436945 | C | T | 10 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(7): Show |
11 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.415+10588G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100436945 | |||||||
| chr4:100437149 | A | G | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+10384T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437149 | |||||||
| chr4:100437237 | T | A | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.415+10296A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437237 | |||||||
| chr4:100437318 | A | G | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+10215T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437318 | |||||||
| chr4:100437351 | A | G | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+10182T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437351 | |||||||
| chr4:100437460 | T | TA | 27 | a0001c0001t0001g0101 a0001c0001t0003g0085 a0001c0001t0003g0102 others(24): Show |
27 | HG00642.hp1 HG01258.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.415+10072dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437460 | |||||||
| chr4:100437460 | T | TCA | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+10072_415+1007 others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437460 | |||||||
| chr4:100437486 | A | G | 132 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(129): Show |
134 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.415+10047T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437486 | |||||||
| chr4:100437496 | G | T | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.415+10037C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437496 | |||||||
| chr4:100437654 | A | G | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+9879T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437654 | |||||||
| chr4:100437767 | C | A | 41 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(38): Show |
42 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.415+9766G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437767 | |||||||
| chr4:100437807 | G | T | 10 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(7): Show |
11 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.415+9726C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437807 | |||||||
| chr4:100437914 | TG | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0185 a0004c0005t0017g0019 others(1): Show |
4 | HG00735.hp1 HG01515.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+9618delC | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100437914 | |||||||
| chr4:100438025 | A | G | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+9508T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438025 | |||||||
| chr4:100438112 | C | T | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415+9421G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438112 | |||||||
| chr4:100438290 | C | T | 1 | a0001c0004t0004g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.415+9243G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438290 | |||||||
| chr4:100438333 | T | C | 1 | a0001c0001t0002g0236 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.415+9200A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438333 | |||||||
| chr4:100438378 | A | T | 1 | a0001c0001t0003g0210 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.415+9155T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438378 | |||||||
| chr4:100438552 | T | C | 1 | a0002c0002t0001g0058 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.415+8981A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438552 | |||||||
| chr4:100438845 | G | A | 1 | a0002c0002t0021g0063 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.415+8688C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438845 | |||||||
| chr4:100438976 | T | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.415+8557A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100438976 | |||||||
| chr4:100439010 | C | T | 1 | a0005c0007t0002g0209 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.415+8523G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439010 | |||||||
| chr4:100439086 | C | G | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 |
3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.415+8447G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439086 | |||||||
| chr4:100439424 | G | A | 1 | a0002c0002t0001g0058 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.415+8109C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439424 | |||||||
| chr4:100439456 | G | T | 17 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(14): Show |
17 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.415+8077C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439456 | |||||||
| chr4:100439553 | T | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.415+7980A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439553 | |||||||
| chr4:100439558 | AT | A | 17 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(14): Show |
17 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.415+7974delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439558 | |||||||
| chr4:100439562 | T | A | 17 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(14): Show |
17 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.415+7971A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439562 | |||||||
| chr4:100439654 | C | A | 2 | a0002c0002t0001g0050 a0002c0002t0001g0051 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.415+7879G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439654 | |||||||
| chr4:100439712 | A | G | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.415+7821T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439712 | |||||||
| chr4:100439842 | C | T | 43 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(40): Show |
44 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.415+7691G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439842 | |||||||
| chr4:100439845 | A | G | 2 | a0001c0001t0038g0211 a0003c0003t0036g0160 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.415+7688T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100439845 | |||||||
| chr4:100440053 | T | TGTGAA | 56 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(53): Show |
57 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.415+7479_415+7480i others(7): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440053 | |||||||
| chr4:100440054 | C | A | 1 | a0002c0002t0001g0105 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.415+7479G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440054 | |||||||
| chr4:100440055 | C | A | 1 | a0002c0002t0001g0105 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.415+7478G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440055 | |||||||
| chr4:100440055 | C | T | 56 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(53): Show |
57 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.415+7478G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440055 | |||||||
| chr4:100440056 | C | A | 56 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(53): Show |
57 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.415+7477G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440056 | |||||||
| chr4:100440057 | A | T | 56 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(53): Show |
57 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.415+7476T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440057 | |||||||
| chr4:100440062 | A | G | 1 | a0002c0002t0001g0088 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.415+7471T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440062 | |||||||
| chr4:100440086 | A | G | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.415+7447T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440086 | |||||||
| chr4:100440199 | A | T | 2 | a0001c0001t0038g0211 a0003c0003t0036g0160 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.415+7334T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440199 | |||||||
| chr4:100440203 | A | G | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.415+7330T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440203 | |||||||
| chr4:100440237 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.415+7296C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440237 | |||||||
| chr4:100440322 | T | C | 1 | a0002c0002t0001g0135 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.415+7211A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440322 | |||||||
| chr4:100440343 | G | A | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+7190C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440343 | |||||||
| chr4:100440394 | C | T | 43 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(40): Show |
44 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.415+7139G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440394 | |||||||
| chr4:100440395 | G | A | 2 | a0002c0002t0001g0056 a0002c0002t0001g0064 |
2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.415+7138C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440395 | |||||||
| chr4:100440439 | G | A | 3 | a0001c0004t0004g0248 a0001c0004t0004g0249 a0002c0006t0004g0048 |
3 | HG02257.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.415+7094C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440439 | |||||||
| chr4:100440568 | T | C | 1 | a0004c0005t0017g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.415+6965A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440568 | |||||||
| chr4:100440607 | G | A | 2 | a0002c0002t0001g0016 a0002c0002t0001g0017 |
2 | NA18946.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.415+6926C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440607 | |||||||
| chr4:100440630 | A | G | 2 | a0001c0001t0004g0251 a0001c0001t0004g0252 |
2 | HG01109.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.415+6903T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440630 | |||||||
| chr4:100440812 | C | T | 16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+6721G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440812 | |||||||
| chr4:100440837 | G | A | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.415+6696C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440837 | |||||||
| chr4:100440872 | T | G | 1 | a0001c0001t0006g0157 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.415+6661A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100440872 | |||||||
| chr4:100441094 | A | C | 30 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(27): Show |
31 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.415+6439T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441094 | |||||||
| chr4:100441121 | A | T | 2 | a0001c0001t0009g0121 a0001c0001t0009g0153 |
2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.415+6412T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441121 | |||||||
| chr4:100441124 | A | G | 2 | a0002c0002t0001g0050 a0002c0002t0001g0051 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.415+6409T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441124 | |||||||
| chr4:100441245 | C | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.415+6288G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441245 | |||||||
| chr4:100441306 | T | C | 4 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(1): Show |
5 | HG01257.hp2 HG01258.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.415+6227A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441306 | |||||||
| chr4:100441322 | A | G | 5 | a0002c0002t0001g0046 a0002c0002t0001g0071 a0002c0002t0001g0074 others(2): Show |
5 | HG01074.hp2 HG01255.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+6211T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441322 | |||||||
| chr4:100441465 | A | G | 16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+6068T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441465 | |||||||
| chr4:100441495 | T | C | 1 | a0001c0001t0002g0229 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.415+6038A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441495 | |||||||
| chr4:100441602 | T | A | 10 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(7): Show |
11 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.415+5931A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441602 | |||||||
| chr4:100441649 | A | T | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.415+5884T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441649 | |||||||
| chr4:100441743 | T | G | 1 | a0002c0002t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.415+5790A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441743 | |||||||
| chr4:100441750 | C | A | 5 | a0001c0001t0008g0116 a0001c0001t0008g0117 a0001c0001t0008g0118 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+5783G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441750 | |||||||
| chr4:100441760 | C | T | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415+5773G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441760 | |||||||
| chr4:100441857 | G | A | 79 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(76): Show |
80 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.415+5676C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441857 | |||||||
| chr4:100441908 | CAT | C | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+5623_415+5624d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441908 | |||||||
| chr4:100441954 | A | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.415+5579T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100441954 | |||||||
| chr4:100442124 | T | G | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+5409A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100442124 | |||||||
| chr4:100442288 | T | C | 41 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(38): Show |
42 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.415+5245A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100442288 | |||||||
| chr4:100442359 | C | T | 129 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(126): Show |
131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.415+5174G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100442359 | |||||||
| chr4:100442509 | T | C | 1 | a0002c0002t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.415+5024A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100442509 | |||||||
| chr4:100442558 | TC | T | 129 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(126): Show |
131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.415+4974delG | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100442558 | |||||||
| chr4:100442586 | T | G | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415+4947A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100442586 | |||||||
| chr4:100442814 | T | TC | 41 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(38): Show |
42 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.415+4718dupG | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100442814 | |||||||
| chr4:100443377 | C | T | 1 | a0004c0005t0017g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.415+4156G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100443377 | |||||||
| chr4:100443378 | G | T | 7 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(4): Show |
8 | HG01109.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.415+4155C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100443378 | |||||||
| chr4:100443420 | G | C | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.415+4113C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100443420 | |||||||
| chr4:100443478 | G | T | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415+4055C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100443478 | |||||||
| chr4:100443532 | T | C | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+4001A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100443532 | |||||||
| chr4:100443753 | G | C | 1 | a0001c0001t0001g0044 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.415+3780C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100443753 | |||||||
| chr4:100443784 | C | A | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415+3749G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100443784 | |||||||
| chr4:100444089 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.415+3444C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444089 | |||||||
| chr4:100444220 | C | T | 1 | a0002c0002t0010g0145 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.415+3313G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444220 | |||||||
| chr4:100444269 | A | G | 3 | a0001c0001t0004g0154 a0001c0001t0004g0156 a0001c0001t0019g0155 |
3 | HG02145.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.415+3264T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444269 | |||||||
| chr4:100444313 | G | A | 1 | a0001c0001t0012g0180 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.415+3220C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444313 | |||||||
| chr4:100444338 | A | G | 230 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(227): Show |
234 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(231): Show |
intron_variant | MODIFIER | c.415+3195T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444338 | |||||||
| chr4:100444388 | A | G | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+3145T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444388 | |||||||
| chr4:100444430 | C | G | 19 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(16): Show |
19 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.415+3103G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444430 | |||||||
| chr4:100444432 | A | G | 43 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(40): Show |
44 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.415+3101T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444432 | |||||||
| chr4:100444733 | C | T | 129 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(126): Show |
131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.415+2800G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444733 | |||||||
| chr4:100444959 | C | T | 227 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(224): Show |
231 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(228): Show |
intron_variant | MODIFIER | c.415+2574G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100444959 | |||||||
| chr4:100445001 | A | T | 45 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(42): Show |
46 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.415+2532T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445001 | |||||||
| chr4:100445124 | T | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.415+2409A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445124 | |||||||
| chr4:100445161 | A | T | 1 | a0002c0002t0001g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.415+2372T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445161 | |||||||
| chr4:100445243 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.415+2290A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445243 | |||||||
| chr4:100445418 | C | T | 229 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(226): Show |
233 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(230): Show |
intron_variant | MODIFIER | c.415+2115G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445418 | |||||||
| chr4:100445503 | C | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.415+2030G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445503 | |||||||
| chr4:100445728 | G | A | 37 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(34): Show |
38 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.415+1805C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445728 | |||||||
| chr4:100445813 | C | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.415+1720G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445813 | |||||||
| chr4:100445896 | A | C | 35 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(32): Show |
35 | HG00639.hp1 HG00673.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.415+1637T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445896 | |||||||
| chr4:100445989 | A | T | 41 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(38): Show |
42 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.415+1544T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100445989 | |||||||
| chr4:100446206 | C | T | 225 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(222): Show |
229 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(226): Show |
intron_variant | MODIFIER | c.415+1327G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446206 | |||||||
| chr4:100446331 | T | TA | 39 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(36): Show |
40 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.415+1201dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446331 | |||||||
| chr4:100446501 | T | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.415+1032A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446501 | |||||||
| chr4:100446514 | T | C | 1 | a0001c0001t0007g0125 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.415+1019A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446514 | |||||||
| chr4:100446519 | T | A | 136 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(133): Show |
138 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.415+1014A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446519 | |||||||
| chr4:100446544 | T | G | 1 | a0001c0001t0002g0032 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.415+989A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446544 | |||||||
| chr4:100446696 | A | C | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.415+837T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446696 | |||||||
| chr4:100446997 | G | T | 39 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(36): Show |
40 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.415+536C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100446997 | |||||||
| chr4:100447058 | C | G | 1 | a0001c0001t0003g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.415+475G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447058 | |||||||
| chr4:100447125 | A | G | 226 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(223): Show |
230 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(227): Show |
intron_variant | MODIFIER | c.415+408T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447125 | |||||||
| chr4:100447127 | T | C | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+406A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447127 | |||||||
| chr4:100447130 | T | C | 1 | a0001c0001t0038g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.415+403A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447130 | |||||||
| chr4:100447171 | C | G | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+362G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447171 | |||||||
| chr4:100447172 | A | G | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+361T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447172 | |||||||
| chr4:100447205 | T | C | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415+328A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447205 | |||||||
| chr4:100447344 | A | G | 129 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(126): Show |
131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.415+189T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447344 | |||||||
| chr4:100447360 | T | C | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.415+173A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447360 | |||||||
| chr4:100447402 | T | C | 19 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(16): Show |
19 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.415+131A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447402 | |||||||
| chr4:100447409 | T | C | 6 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(3): Show |
6 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.415+124A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447409 | |||||||
| chr4:100447476 | T | G | 17 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(14): Show |
17 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.415+57A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447476 | |||||||
| chr4:100447504 | A | G | 41 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(38): Show |
42 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.415+29T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 5/11 | chr4 | 100447504 | |||||||
| chr4:100447822 | C | T | 2 | a0001c0001t0005g0256 a0001c0001t0005g0257 |
2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.377-251G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100447822 | |||||||
| chr4:100447834 | C | T | 1 | a0002c0002t0009g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.377-263G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100447834 | |||||||
| chr4:100447893 | G | A | 1 | a0002c0006t0004g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.377-322C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100447893 | |||||||
| chr4:100448016 | T | C | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.377-445A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448016 | |||||||
| chr4:100448021 | A | G | 2 | a0001c0001t0002g0021 a0001c0001t0002g0041 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.377-450T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448021 | |||||||
| chr4:100448468 | T | C | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.377-897A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448468 | |||||||
| chr4:100448557 | C | A | 6 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(3): Show |
6 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-986G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448557 | |||||||
| chr4:100448698 | C | T | 1 | a0002c0002t0037g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.377-1127G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448698 | |||||||
| chr4:100448730 | G | A | 6 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(3): Show |
6 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-1159C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448730 | |||||||
| chr4:100448795 | T | TTTTC | 23 | a0001c0001t0002g0003 a0001c0001t0002g0181 a0001c0001t0002g0184 others(20): Show |
24 | HG00639.hp1 HG00673.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | |||||||
| chr4:100448795 | T | TTTTCTTT others(1): Show |
13 | a0001c0001t0002g0176 a0001c0001t0002g0179 a0001c0001t0002g0203 others(10): Show |
14 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(10): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | |||||||
| chr4:100448795 | T | TTTTCTTT others(5): Show |
4 | a0001c0001t0002g0177 a0001c0001t0002g0230 a0001c0001t0012g0180 others(1): Show |
4 | HG02148.hp1 HG02486.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | |||||||
| chr4:100448795 | T | TTTTCTTT others(9): Show |
56 | a0001c0001t0001g0182 a0001c0001t0002g0007 a0001c0001t0002g0010 others(53): Show |
56 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(18): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | |||||||
| chr4:100448795 | T | TTTTCTTT others(13): Show |
69 | a0001c0001t0001g0185 a0001c0001t0001g0195 a0001c0001t0001g0196 others(66): Show |
70 | HG00597.hp2 HG00735.hp1 HG01074.hp2 others(67): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(22): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | |||||||
| chr4:100448795 | T | TTTTCTTT others(17): Show |
9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0004g0253 others(6): Show |
9 | HG00408.hp1 HG00408.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(26): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | |||||||
| chr4:100448795 | T | TTTTCTTT others(21): Show |
4 | a0001c0001t0004g0004 a0001c0001t0004g0251 a0002c0002t0001g0042 others(1): Show |
5 | HG01109.hp2 HG02148.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(30): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | |||||||
| chr4:100448795 | T | TTTTCTTT others(25): Show |
1 | a0002c0002t0001g0062 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.377-1225_377-1224i others(34): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | |||||||
| chr4:100448795 | T | TTTTCTTT others(29): Show |
2 | a0001c0001t0004g0252 a0001c0001t0028g0175 |
2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.377-1225_377-1224i others(38): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | |||||||
| chr4:100448795 | T | TTTTCTTT others(9): Show |
1 | a0001c0001t0011g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.377-1225_377-1224i others(18): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | |||||||
| chr4:100448795 | T | TTTTCTTT others(17): Show |
10 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0191 others(7): Show |
10 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(26): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | |||||||
| chr4:100448795 | T | TTTTCTTT others(21): Show |
7 | a0001c0001t0005g0183 a0001c0001t0005g0189 a0001c0001t0005g0244 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(30): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | |||||||
| chr4:100448795 | T | TTTTCTTT others(25): Show |
4 | a0001c0001t0005g0201 a0001c0001t0005g0257 a0001c0001t0011g0112 others(1): Show |
4 | HG02055.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-1225_377-1224i others(34): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448795 | |||||||
| chr4:100448796 | C | T | 46 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(43): Show |
47 | HG00639.hp1 HG00673.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.377-1225G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448796 | |||||||
| chr4:100448800 | C | T | 23 | a0001c0001t0002g0127 a0001c0001t0002g0129 a0001c0001t0002g0194 others(20): Show |
23 | HG00673.hp1 HG00741.hp1 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.377-1229G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448800 | |||||||
| chr4:100448820 | C | T | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 |
3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.377-1249G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448820 | |||||||
| chr4:100448822 | T | TCCTTCCT others(33): Show |
1 | a0001c0001t0003g0212 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.377-1252_377-1251i others(42): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | |||||||
| chr4:100448822 | T | TCCTTCCT others(33): Show |
5 | a0001c0001t0003g0207 a0001c0001t0003g0255 a0001c0001t0009g0242 others(2): Show |
5 | HG02559.hp2 HG03209.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.377-1252_377-1251i others(42): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | |||||||
| chr4:100448822 | T | TCCTTCCT others(37): Show |
5 | a0001c0001t0001g0101 a0001c0001t0003g0186 a0001c0001t0003g0206 others(2): Show |
5 | HG00642.hp1 HG01258.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.377-1252_377-1251i others(46): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | |||||||
| chr4:100448822 | T | TCCTTCCT others(33): Show |
1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.377-1252_377-1251i others(42): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | |||||||
| chr4:100448822 | T | TCCTTCCT others(37): Show |
2 | a0001c0001t0003g0210 a0001c0001t0009g0121 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.377-1252_377-1251i others(46): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | |||||||
| chr4:100448822 | T | TCCTTCCT others(41): Show |
12 | a0001c0001t0002g0187 a0001c0001t0002g0217 a0001c0001t0003g0102 others(9): Show |
12 | HG01516.hp1 HG01934.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.377-1252_377-1251i others(50): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | |||||||
| chr4:100448822 | T | TCCTTCCT others(41): Show |
1 | a0001c0001t0009g0153 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.377-1252_377-1251i others(50): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | |||||||
| chr4:100448822 | T | TCCTTCCT others(45): Show |
1 | a0001c0001t0003g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.377-1252_377-1251i others(54): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | |||||||
| chr4:100448822 | T | TCCTTCCT others(49): Show |
1 | a0001c0001t0003g0085 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.377-1252_377-1251i others(58): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | |||||||
| chr4:100448822 | T | TCCTTCCT others(53): Show |
1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.377-1252_377-1251i others(62): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | |||||||
| chr4:100448822 | TCCTC | T | 9 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0133 others(6): Show |
9 | HG00673.hp1 HG02056.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.377-1255_377-1252d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448822 | |||||||
| chr4:100448824 | C | T | 126 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(123): Show |
128 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.377-1253G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448824 | |||||||
| chr4:100448826 | C | T | 217 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(214): Show |
221 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(218): Show |
intron_variant | MODIFIER | c.377-1255G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448826 | |||||||
| chr4:100448830 | C | T | 226 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(223): Show |
230 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(227): Show |
intron_variant | MODIFIER | c.377-1259G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448830 | |||||||
| chr4:100448834 | C | T | 226 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(223): Show |
230 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(227): Show |
intron_variant | MODIFIER | c.377-1263G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448834 | |||||||
| chr4:100448838 | C | T | 226 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(223): Show |
230 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(227): Show |
intron_variant | MODIFIER | c.377-1267G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448838 | |||||||
| chr4:100448839 | C | A | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.377-1268G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448839 | |||||||
| chr4:100448842 | C | T | 226 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(223): Show |
230 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(227): Show |
intron_variant | MODIFIER | c.377-1271G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448842 | |||||||
| chr4:100448990 | C | G | 1 | a0001c0001t0002g0239 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.377-1419G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100448990 | |||||||
| chr4:100449050 | A | G | 6 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(3): Show |
6 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-1479T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100449050 | |||||||
| chr4:100449252 | G | A | 1 | a0002c0002t0001g0099 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.377-1681C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100449252 | |||||||
| chr4:100449345 | A | G | 1 | a0002c0002t0001g0055 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.377-1774T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100449345 | |||||||
| chr4:100449470 | C | T | 129 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(126): Show |
131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.377-1899G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100449470 | |||||||
| chr4:100449519 | A | G | 1 | a0002c0002t0022g0234 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.377-1948T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100449519 | |||||||
| chr4:100449930 | A | C | 1 | a0001c0001t0004g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.377-2359T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100449930 | |||||||
| chr4:100450184 | G | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.377-2613C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100450184 | |||||||
| chr4:100450335 | C | T | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-2764G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100450335 | |||||||
| chr4:100450346 | C | A | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-2775G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100450346 | |||||||
| chr4:100450660 | T | G | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.377-3089A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100450660 | |||||||
| chr4:100450835 | T | C | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-3264A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100450835 | |||||||
| chr4:100451227 | T | TAAG | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-3659_377-3657d others(5): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451227 | |||||||
| chr4:100451307 | T | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.377-3736A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451307 | |||||||
| chr4:100451308 | G | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.377-3737C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451308 | |||||||
| chr4:100451384 | T | A | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-3813A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451384 | |||||||
| chr4:100451449 | T | A | 4 | a0001c0001t0015g0022 a0001c0001t0015g0115 a0002c0002t0016g0110 others(1): Show |
4 | HG02922.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-3878A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451449 | |||||||
| chr4:100451653 | T | C | 1 | a0002c0002t0001g0170 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.377-4082A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451653 | |||||||
| chr4:100451800 | A | G | 13 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0133 others(10): Show |
13 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.377-4229T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451800 | |||||||
| chr4:100451936 | T | A | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-4365A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100451936 | |||||||
| chr4:100452156 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.377-4585C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452156 | |||||||
| chr4:100452248 | T | C | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.377-4677A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452248 | |||||||
| chr4:100452469 | G | A | 1 | a0001c0001t0003g0216 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.377-4898C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452469 | |||||||
| chr4:100452530 | C | T | 9 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0007g0163 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.377-4959G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452530 | |||||||
| chr4:100452570 | G | T | 58 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(55): Show |
59 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.377-4999C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452570 | |||||||
| chr4:100452573 | A | G | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-5002T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452573 | |||||||
| chr4:100452673 | G | A | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-5102C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452673 | |||||||
| chr4:100452894 | C | G | 10 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(7): Show |
11 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.377-5323G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100452894 | |||||||
| chr4:100453066 | A | G | 1 | a0001c0001t0034g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.377-5495T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453066 | |||||||
| chr4:100453081 | G | T | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-5510C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453081 | |||||||
| chr4:100453117 | A | T | 1 | a0001c0001t0002g0187 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.377-5546T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453117 | |||||||
| chr4:100453151 | A | C | 1 | a0001c0001t0003g0210 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.377-5580T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453151 | |||||||
| chr4:100453187 | A | C | 3 | a0001c0001t0003g0210 a0001c0001t0015g0022 a0001c0001t0015g0115 |
3 | HG02965.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-5616T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453187 | |||||||
| chr4:100453302 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.377-5731T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453302 | |||||||
| chr4:100453719 | A | T | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-6148T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453719 | |||||||
| chr4:100453847 | A | C | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-6276T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453847 | |||||||
| chr4:100453870 | T | C | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-6299A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453870 | |||||||
| chr4:100453915 | C | T | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.377-6344G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453915 | |||||||
| chr4:100453940 | G | A | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-6369C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100453940 | |||||||
| chr4:100454060 | T | A | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-6489A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454060 | |||||||
| chr4:100454061 | A | T | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-6490T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454061 | |||||||
| chr4:100454179 | TA | T | 16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.377-6609delT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454179 | |||||||
| chr4:100454188 | T | A | 11 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.377-6617A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454188 | |||||||
| chr4:100454238 | C | CA | 34 | a0001c0001t0002g0036 a0001c0001t0002g0187 a0001c0001t0002g0193 others(31): Show |
34 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.377-6668dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454238 | |||||||
| chr4:100454238 | C | CAA | 64 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(61): Show |
65 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.377-6669_377-6668d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454238 | |||||||
| chr4:100454238 | C | CAAA | 21 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0007g0130 others(18): Show |
21 | HG01123.hp1 HG01169.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.377-6670_377-6668d others(5): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454238 | |||||||
| chr4:100454238 | CA | C | 37 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(34): Show |
39 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.377-6668delT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454238 | |||||||
| chr4:100454540 | T | A | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.377-6969A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454540 | |||||||
| chr4:100454679 | T | C | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-7108A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454679 | |||||||
| chr4:100454710 | A | G | 1 | a0002c0002t0001g0058 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.377-7139T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454710 | |||||||
| chr4:100454852 | T | C | 3 | a0001c0001t0028g0175 a0001c0001t0038g0211 a0003c0003t0036g0160 |
3 | HG02486.hp1 HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.377-7281A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100454852 | |||||||
| chr4:100455148 | C | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.377-7577G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455148 | |||||||
| chr4:100455197 | G | T | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-7626C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455197 | |||||||
| chr4:100455476 | T | C | 95 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(92): Show |
96 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.377-7905A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455476 | |||||||
| chr4:100455509 | G | GT | 61 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(58): Show |
62 | HG00597.hp1 HG00673.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.377-7939dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455509 | |||||||
| chr4:100455509 | GT | G | 6 | a0001c0001t0005g0174 a0001c0001t0007g0130 a0001c0001t0038g0211 others(3): Show |
6 | HG02148.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-7939delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455509 | |||||||
| chr4:100455530 | A | C | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.377-7959T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455530 | |||||||
| chr4:100455540 | A | AT | 235 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(232): Show |
239 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(236): Show |
intron_variant | MODIFIER | c.377-7970_377-7969i others(3): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455540 | |||||||
| chr4:100455561 | C | T | 1 | a0001c0001t0005g0244 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.377-7990G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455561 | |||||||
| chr4:100455607 | C | T | 2 | a0004c0005t0017g0019 a0004c0005t0017g0020 |
2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.377-8036G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455607 | |||||||
| chr4:100455676 | A | G | 2 | a0002c0002t0001g0065 a0002c0002t0001g0081 |
2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.377-8105T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455676 | |||||||
| chr4:100455685 | T | C | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.377-8114A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100455685 | |||||||
| chr4:100456010 | G | C | 1 | a0002c0002t0001g0042 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.377-8439C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456010 | |||||||
| chr4:100456173 | G | T | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.377-8602C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456173 | |||||||
| chr4:100456327 | T | G | 2 | a0002c0002t0001g0061 a0002c0002t0001g0066 |
2 | HG02056.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.377-8756A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456327 | |||||||
| chr4:100456436 | T | C | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.377-8865A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456436 | |||||||
| chr4:100456479 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.377-8908G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456479 | |||||||
| chr4:100456543 | C | A | 221 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(218): Show |
225 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(222): Show |
intron_variant | MODIFIER | c.376+8880G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456543 | |||||||
| chr4:100456594 | T | A | 2 | a0002c0002t0001g0065 a0002c0002t0001g0081 |
2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.376+8829A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456594 | |||||||
| chr4:100456990 | C | T | 57 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(54): Show |
58 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.376+8433G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100456990 | |||||||
| chr4:100457038 | G | A | 10 | a0001c0001t0004g0004 a0001c0001t0004g0018 a0001c0001t0004g0131 others(7): Show |
11 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.376+8385C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457038 | |||||||
| chr4:100457071 | G | GT | 5 | a0001c0001t0002g0122 a0001c0001t0003g0220 a0002c0002t0001g0017 others(2): Show |
5 | HG00735.hp2 HG01934.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+8351dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457071 | |||||||
| chr4:100457190 | T | TTG | 17 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(14): Show |
17 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.376+8231_376+8232d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457190 | |||||||
| chr4:100457190 | T | TTGTG | 3 | a0001c0001t0027g0247 a0004c0005t0017g0019 a0004c0005t0017g0020 |
3 | HG00735.hp1 HG00741.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.376+8229_376+8232d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457190 | |||||||
| chr4:100457190 | TTGTG | T | 6 | a0001c0001t0002g0122 a0001c0001t0011g0109 a0001c0001t0011g0112 others(3): Show |
6 | HG00735.hp2 HG02486.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.376+8229_376+8232d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457190 | |||||||
| chr4:100457205 | TGTGTGTG others(5): Show |
T | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.376+8206_376+8217d others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457205 | |||||||
| chr4:100457213 | TGTGC | T | 135 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(132): Show |
138 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.376+8206_376+8209d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457213 | |||||||
| chr4:100457215 | TGC | T | 28 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(25): Show |
28 | HG00639.hp1 HG00673.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.376+8206_376+8207d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457215 | |||||||
| chr4:100457217 | C | T | 58 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(55): Show |
59 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.376+8206G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457217 | |||||||
| chr4:100457241 | A | T | 4 | a0001c0001t0002g0127 a0001c0001t0002g0129 a0001c0001t0013g0246 others(1): Show |
4 | HG00741.hp1 HG01361.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.376+8182T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457241 | |||||||
| chr4:100457470 | T | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.376+7953A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457470 | |||||||
| chr4:100457629 | C | T | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.376+7794G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457629 | |||||||
| chr4:100457865 | T | A | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.376+7558A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457865 | |||||||
| chr4:100457945 | C | T | 1 | a0001c0001t0008g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.376+7478G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457945 | |||||||
| chr4:100457946 | G | A | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.376+7477C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457946 | |||||||
| chr4:100457974 | G | A | 1 | a0002c0002t0006g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.376+7449C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100457974 | |||||||
| chr4:100458122 | A | C | 1 | a0001c0001t0005g0200 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.376+7301T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100458122 | |||||||
| chr4:100458690 | C | T | 3 | a0001c0001t0028g0175 a0001c0001t0038g0211 a0003c0003t0036g0160 |
3 | HG02486.hp1 HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.376+6733G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100458690 | |||||||
| chr4:100458784 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.376+6639G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100458784 | |||||||
| chr4:100458944 | G | A | 1 | a0001c0001t0003g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.376+6479C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100458944 | |||||||
| chr4:100458991 | G | C | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.376+6432C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100458991 | |||||||
| chr4:100459016 | G | GA | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.376+6406dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459016 | |||||||
| chr4:100459054 | G | A | 16 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(13): Show |
16 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.376+6369C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459054 | |||||||
| chr4:100459055 | G | A | 2 | a0002c0002t0001g0056 a0002c0002t0001g0064 |
2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.376+6368C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459055 | |||||||
| chr4:100459168 | GCTCT | G | 6 | a0001c0001t0001g0101 a0001c0001t0003g0206 a0001c0001t0003g0215 others(3): Show |
6 | HG00642.hp1 HG01496.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.376+6251_376+6254d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCT | G | 6 | a0001c0001t0002g0217 a0001c0001t0003g0102 a0001c0001t0003g0186 others(3): Show |
6 | HG01258.hp2 HG01943.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.376+6249_376+6254d others(8): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCTC others(1): Show |
G | 5 | a0001c0001t0002g0222 a0001c0001t0003g0212 a0001c0001t0004g0018 others(2): Show |
5 | HG01123.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+6247_376+6254d others(10): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCTC others(3): Show |
G | 6 | a0001c0001t0002g0181 a0001c0001t0003g0207 a0001c0001t0003g0210 others(3): Show |
6 | HG01192.hp1 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.376+6245_376+6254d others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCTC others(5): Show |
G | 13 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0178 others(10): Show |
14 | HG01109.hp2 HG01167.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.376+6243_376+6254d others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCTC others(7): Show |
G | 3 | a0001c0001t0002g0230 a0001c0001t0002g0236 a0001c0001t0011g0114 |
3 | HG01099.hp1 HG02486.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.376+6241_376+6254d others(16): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCTC others(9): Show |
G | 7 | a0001c0001t0002g0226 a0001c0001t0003g0235 a0001c0001t0003g0255 others(4): Show |
7 | HG02602.hp2 HG03041.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.376+6239_376+6254d others(18): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCTC others(11): Show |
G | 25 | a0001c0001t0002g0003 a0001c0001t0002g0127 a0001c0001t0002g0129 others(22): Show |
26 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.376+6237_376+6254d others(20): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCTC others(13): Show |
G | 5 | a0001c0001t0002g0221 a0001c0001t0011g0109 a0001c0001t0011g0113 others(2): Show |
5 | HG03209.hp1 HG03453.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+6235_376+6254d others(22): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCTC others(15): Show |
G | 3 | a0001c0001t0002g0122 a0001c0001t0032g0254 a0002c0002t0004g0162 |
3 | HG00735.hp2 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.376+6233_376+6254d others(24): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCTC others(17): Show |
G | 1 | a0001c0004t0004g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.376+6231_376+6254d others(26): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCTC others(19): Show |
G | 3 | a0003c0003t0004g0158 a0004c0005t0017g0019 a0004c0005t0017g0020 |
3 | HG00735.hp1 HG01515.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.376+6229_376+6254d others(28): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCTC others(21): Show |
G | 2 | a0001c0001t0002g0013 a0001c0001t0029g0159 |
2 | HG01975.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.376+6227_376+6254d others(30): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCTC others(23): Show |
G | 6 | a0001c0001t0002g0161 a0001c0001t0028g0175 a0001c0001t0038g0211 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.376+6225_376+6254d others(32): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCTC others(25): Show |
G | 145 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(142): Show |
147 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.376+6223_376+6254d others(34): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459168 | GCTCTCTC others(27): Show |
G | 16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.376+6221_376+6254d others(36): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459168 | |||||||
| chr4:100459226 | T | C | 1 | a0001c0001t0002g0031 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.376+6197A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459226 | |||||||
| chr4:100459304 | C | CAT | 222 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(219): Show |
226 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(223): Show |
intron_variant | MODIFIER | c.376+6117_376+6118d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459304 | |||||||
| chr4:100459538 | T | C | 221 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(218): Show |
225 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(222): Show |
intron_variant | MODIFIER | c.376+5885A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459538 | |||||||
| chr4:100459632 | G | A | 3 | a0001c0001t0028g0175 a0001c0001t0038g0211 a0003c0003t0036g0160 |
3 | HG02486.hp1 HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.376+5791C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459632 | |||||||
| chr4:100459734 | G | A | 214 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(211): Show |
218 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(215): Show |
intron_variant | MODIFIER | c.376+5689C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100459734 | |||||||
| chr4:100460064 | T | C | 1 | a0002c0002t0026g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.376+5359A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460064 | |||||||
| chr4:100460139 | C | G | 1 | a0001c0001t0012g0238 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.376+5284G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460139 | |||||||
| chr4:100460139 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.376+5284G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460139 | |||||||
| chr4:100460160 | A | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.376+5263T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460160 | |||||||
| chr4:100460370 | A | G | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.376+5053T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460370 | |||||||
| chr4:100460519 | G | A | 2 | a0002c0002t0001g0056 a0002c0002t0001g0064 |
2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.376+4904C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460519 | |||||||
| chr4:100460542 | G | C | 120 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(117): Show |
122 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.376+4881C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460542 | |||||||
| chr4:100460613 | G | A | 236 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(233): Show |
240 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(237): Show |
intron_variant | MODIFIER | c.376+4810C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460613 | |||||||
| chr4:100460705 | G | A | 1 | a0002c0002t0001g0105 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.376+4718C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460705 | |||||||
| chr4:100460796 | T | C | 2 | a0001c0001t0038g0211 a0003c0003t0036g0160 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.376+4627A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460796 | |||||||
| chr4:100460962 | T | C | 2 | a0001c0001t0002g0039 a0001c0001t0002g0040 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.376+4461A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100460962 | |||||||
| chr4:100461457 | A | G | 134 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(131): Show |
136 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.376+3966T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100461457 | |||||||
| chr4:100461682 | A | C | 124 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(121): Show |
126 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.376+3741T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100461682 | |||||||
| chr4:100461746 | C | T | 196 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(193): Show |
200 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.376+3677G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100461746 | |||||||
| chr4:100461935 | C | T | 196 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(193): Show |
200 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.376+3488G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100461935 | |||||||
| chr4:100462021 | A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.376+3402T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462021 | |||||||
| chr4:100462051 | T | C | 1 | a0002c0002t0037g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.376+3372A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462051 | |||||||
| chr4:100462055 | A | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.376+3368T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462055 | |||||||
| chr4:100462211 | C | T | 1 | a0001c0001t0015g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.376+3212G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462211 | |||||||
| chr4:100462337 | T | C | 19 | a0002c0002t0001g0086 a0002c0002t0001g0087 a0002c0002t0001g0088 others(16): Show |
19 | HG00597.hp2 HG01192.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.376+3086A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462337 | |||||||
| chr4:100462357 | A | G | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.376+3066T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462357 | |||||||
| chr4:100462475 | T | C | 196 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(193): Show |
200 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.376+2948A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462475 | |||||||
| chr4:100462559 | C | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.376+2864G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462559 | |||||||
| chr4:100462578 | T | C | 2 | a0001c0001t0006g0133 a0001c0001t0006g0134 |
2 | HG02735.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.376+2845A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462578 | |||||||
| chr4:100462619 | C | T | 5 | a0001c0001t0008g0116 a0001c0001t0008g0117 a0001c0001t0008g0118 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+2804G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100462619 | |||||||
| chr4:100463053 | T | C | 1 | a0001c0001t0011g0109 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.376+2370A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463053 | |||||||
| chr4:100463334 | T | G | 126 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(123): Show |
128 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.376+2089A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463334 | |||||||
| chr4:100463384 | C | A | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.376+2039G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463384 | |||||||
| chr4:100463403 | G | T | 11 | a0001c0001t0004g0004 a0001c0001t0004g0131 a0001c0001t0004g0250 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.376+2020C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463403 | |||||||
| chr4:100463511 | C | T | 5 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(2): Show |
5 | HG01975.hp1 HG02922.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+1912G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463511 | |||||||
| chr4:100463514 | C | T | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.376+1909G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463514 | |||||||
| chr4:100463689 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.376+1734G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463689 | |||||||
| chr4:100463705 | A | T | 3 | a0001c0001t0009g0121 a0001c0001t0009g0242 a0001c0001t0009g0243 |
3 | HG02559.hp2 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.376+1718T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463705 | |||||||
| chr4:100463810 | C | T | 121 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(118): Show |
123 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.376+1613G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463810 | |||||||
| chr4:100463864 | T | C | 2 | a0004c0005t0017g0019 a0004c0005t0017g0020 |
2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.376+1559A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463864 | |||||||
| chr4:100463918 | C | G | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.376+1505G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100463918 | |||||||
| chr4:100464151 | AC | A | 9 | a0001c0001t0004g0004 a0001c0001t0004g0131 a0001c0001t0004g0250 others(6): Show |
10 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.376+1271delG | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100464151 | |||||||
| chr4:100464252 | C | A | 196 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(193): Show |
200 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.376+1171G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100464252 | |||||||
| chr4:100464312 | C | T | 2 | a0001c0001t0028g0175 a0003c0003t0036g0160 |
2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.376+1111G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100464312 | |||||||
| chr4:100464346 | C | T | 196 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(193): Show |
200 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.376+1077G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100464346 | |||||||
| chr4:100464423 | A | G | 1 | a0001c0001t0002g0010 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.376+1000T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100464423 | |||||||
| chr4:100464872 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.376+551T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100464872 | |||||||
| chr4:100465137 | A | C | 11 | a0001c0001t0004g0004 a0001c0001t0004g0131 a0001c0001t0004g0250 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.376+286T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 4/11 | chr4 | 100465137 | |||||||
| chr4:100465629 | G | T | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.260-90C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100465629 | |||||||
| chr4:100465788 | C | T | 3 | a0003c0003t0004g0158 a0003c0003t0035g0198 a0003c0003t0036g0160 |
3 | HG02615.hp2 HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.260-249G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100465788 | |||||||
| chr4:100465976 | G | A | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-437C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100465976 | |||||||
| chr4:100466052 | A | G | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 |
3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.260-513T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466052 | |||||||
| chr4:100466067 | T | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.260-528A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466067 | |||||||
| chr4:100466096 | GA | G | 125 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(122): Show |
127 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.260-558delT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466096 | |||||||
| chr4:100466214 | G | GT | 10 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(7): Show |
11 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-676dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466214 | |||||||
| chr4:100466215 | T | C | 1 | a0001c0001t0002g0228 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.260-676A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466215 | |||||||
| chr4:100466268 | C | G | 3 | a0003c0003t0004g0158 a0003c0003t0035g0198 a0003c0003t0036g0160 |
3 | HG02615.hp2 HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.260-729G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466268 | |||||||
| chr4:100466631 | A | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.260-1092T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466631 | |||||||
| chr4:100466800 | G | A | 2 | a0003c0003t0004g0158 a0003c0003t0035g0198 |
2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.260-1261C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466800 | |||||||
| chr4:100466808 | T | G | 2 | a0001c0001t0003g0210 a0001c0001t0038g0211 |
2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.260-1269A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466808 | |||||||
| chr4:100466991 | G | A | 121 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(118): Show |
123 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.260-1452C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100466991 | |||||||
| chr4:100467170 | T | A | 1 | a0002c0002t0010g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.260-1631A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467170 | |||||||
| chr4:100467303 | A | G | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-1764T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467303 | |||||||
| chr4:100467454 | G | A | 38 | a0001c0001t0001g0182 a0001c0001t0002g0003 a0001c0001t0002g0176 others(35): Show |
39 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.260-1915C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467454 | |||||||
| chr4:100467460 | C | T | 89 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(86): Show |
90 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.260-1921G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467460 | |||||||
| chr4:100467540 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.260-2001C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467540 | |||||||
| chr4:100467635 | T | C | 1 | a0001c0001t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.260-2096A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467635 | |||||||
| chr4:100467638 | C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.260-2099G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467638 | |||||||
| chr4:100467681 | C | CA | 70 | a0001c0001t0001g0182 a0001c0001t0001g0195 a0001c0001t0002g0003 others(67): Show |
72 | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.260-2143dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467681 | |||||||
| chr4:100467681 | C | CAA | 21 | a0001c0001t0002g0127 a0001c0001t0002g0129 a0001c0001t0002g0181 others(18): Show |
21 | HG00639.hp1 HG01192.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.260-2144_260-2143d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100467681 | |||||||
| chr4:100468073 | G | T | 1 | a0002c0002t0037g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.260-2534C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468073 | |||||||
| chr4:100468153 | G | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0012g0026 |
3 | HG00738.hp1 HG01106.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.260-2614C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468153 | |||||||
| chr4:100468217 | G | A | 1 | a0001c0001t0006g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.260-2678C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468217 | |||||||
| chr4:100468296 | G | A | 2 | a0003c0003t0004g0158 a0003c0003t0035g0198 |
2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.260-2757C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468296 | |||||||
| chr4:100468297 | T | A | 1 | a0002c0002t0001g0144 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.260-2758A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468297 | |||||||
| chr4:100468372 | T | C | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.260-2833A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468372 | |||||||
| chr4:100468414 | T | G | 3 | a0001c0001t0009g0121 a0001c0001t0009g0242 a0001c0001t0009g0243 |
3 | HG02559.hp2 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.260-2875A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468414 | |||||||
| chr4:100468443 | A | T | 1 | a0001c0001t0002g0245 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.260-2904T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468443 | |||||||
| chr4:100468674 | T | A | 196 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(193): Show |
200 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.260-3135A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468674 | |||||||
| chr4:100468708 | C | G | 196 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(193): Show |
200 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.260-3169G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100468708 | |||||||
| chr4:100469169 | C | A | 40 | a0001c0001t0001g0182 a0001c0001t0002g0003 a0001c0001t0002g0176 others(37): Show |
41 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.260-3630G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469169 | |||||||
| chr4:100469213 | C | T | 59 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(56): Show |
60 | HG00408.hp1 HG00408.hp2 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.260-3674G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469213 | |||||||
| chr4:100469314 | T | C | 7 | a0002c0002t0001g0139 a0002c0002t0001g0144 a0002c0002t0001g0146 others(4): Show |
7 | HG01109.hp1 HG01123.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-3775A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469314 | |||||||
| chr4:100469358 | G | C | 196 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(193): Show |
200 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.260-3819C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469358 | |||||||
| chr4:100469418 | T | A | 1 | a0001c0001t0006g0006 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.260-3879A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469418 | |||||||
| chr4:100469477 | AAAATGAA others(171): Show |
A | 58 | a0001c0001t0001g0182 a0001c0001t0002g0003 a0001c0001t0002g0127 others(55): Show |
59 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-4116_260-3939d others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469477 | |||||||
| chr4:100469781 | T | G | 196 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(193): Show |
200 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.260-4242A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469781 | |||||||
| chr4:100469786 | A | G | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-4247T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469786 | |||||||
| chr4:100469856 | C | T | 199 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(196): Show |
203 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(200): Show |
intron_variant | MODIFIER | c.260-4317G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469856 | |||||||
| chr4:100469894 | C | T | 196 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(193): Show |
200 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.260-4355G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469894 | |||||||
| chr4:100469948 | T | G | 58 | a0001c0001t0001g0182 a0001c0001t0002g0003 a0001c0001t0002g0127 others(55): Show |
59 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.260-4409A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469948 | |||||||
| chr4:100469959 | A | G | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.260-4420T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100469959 | |||||||
| chr4:100470076 | C | A | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.260-4537G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470076 | |||||||
| chr4:100470103 | G | C | 1 | a0002c0002t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.260-4564C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470103 | |||||||
| chr4:100470214 | TAACA | T | 11 | a0001c0001t0004g0004 a0001c0001t0004g0131 a0001c0001t0004g0250 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.260-4679_260-4676d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470214 | |||||||
| chr4:100470263 | T | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.260-4724A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470263 | |||||||
| chr4:100470313 | C | A | 198 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(195): Show |
202 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(199): Show |
intron_variant | MODIFIER | c.259+4725G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470313 | |||||||
| chr4:100470322 | C | G | 6 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0223 others(3): Show |
6 | HG00597.hp1 HG00673.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+4716G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470322 | |||||||
| chr4:100470378 | T | TAAAA | 179 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(176): Show |
182 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(179): Show |
intron_variant | MODIFIER | c.259+4656_259+4659d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470378 | |||||||
| chr4:100470378 | T | TAAAAA | 11 | a0001c0001t0004g0004 a0001c0001t0004g0131 a0001c0001t0004g0250 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.259+4655_259+4659d others(7): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470378 | |||||||
| chr4:100470391 | A | T | 1 | a0001c0001t0002g0230 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.259+4647T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470391 | |||||||
| chr4:100470403 | G | T | 1 | a0002c0002t0001g0144 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.259+4635C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470403 | |||||||
| chr4:100470439 | T | C | 195 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(192): Show |
199 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.259+4599A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470439 | |||||||
| chr4:100470593 | T | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.259+4445A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470593 | |||||||
| chr4:100470897 | G | A | 121 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(118): Show |
123 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.259+4141C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470897 | |||||||
| chr4:100470943 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.259+4095G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470943 | |||||||
| chr4:100470999 | G | T | 14 | a0001c0001t0002g0021 a0001c0001t0002g0024 a0001c0001t0002g0025 others(11): Show |
14 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+4039C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100470999 | |||||||
| chr4:100471082 | A | G | 11 | a0001c0001t0004g0004 a0001c0001t0004g0131 a0001c0001t0004g0250 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.259+3956T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471082 | |||||||
| chr4:100471100 | C | A | 196 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(193): Show |
200 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.259+3938G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471100 | |||||||
| chr4:100471325 | C | T | 1 | a0001c0001t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.259+3713G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471325 | |||||||
| chr4:100471335 | G | A | 5 | a0001c0001t0002g0122 a0001c0001t0004g0154 a0001c0001t0004g0156 others(2): Show |
5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+3703C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471335 | |||||||
| chr4:100471424 | A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259+3614T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471424 | |||||||
| chr4:100471505 | A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259+3533T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471505 | |||||||
| chr4:100471507 | A | G | 3 | a0001c0001t0006g0128 a0001c0001t0006g0149 a0001c0001t0033g0141 |
3 | HG00673.hp1 HG02056.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.259+3531T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471507 | |||||||
| chr4:100471564 | A | G | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.259+3474T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471564 | |||||||
| chr4:100471580 | C | A | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.259+3458G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471580 | |||||||
| chr4:100471622 | C | T | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259+3416G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471622 | |||||||
| chr4:100471844 | A | G | 2 | a0002c0002t0001g0050 a0002c0002t0001g0051 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.259+3194T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471844 | |||||||
| chr4:100471860 | C | A | 2 | a0003c0003t0004g0158 a0003c0003t0035g0198 |
2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.259+3178G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471860 | |||||||
| chr4:100471903 | C | T | 1 | a0002c0002t0007g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.259+3135G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471903 | |||||||
| chr4:100471904 | G | A | 196 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(193): Show |
200 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.259+3134C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100471904 | |||||||
| chr4:100472091 | A | G | 196 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(193): Show |
200 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(197): Show |
intron_variant | MODIFIER | c.259+2947T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472091 | |||||||
| chr4:100472191 | T | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259+2847A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472191 | |||||||
| chr4:100472285 | T | C | 1 | a0001c0001t0002g0029 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.259+2753A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472285 | |||||||
| chr4:100472349 | T | A | 15 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(12): Show |
15 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.259+2689A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472349 | |||||||
| chr4:100472543 | T | C | 1 | a0001c0001t0003g0186 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.259+2495A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472543 | |||||||
| chr4:100472587 | C | A | 11 | a0001c0001t0004g0004 a0001c0001t0004g0131 a0001c0001t0004g0250 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.259+2451G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472587 | |||||||
| chr4:100472783 | T | A | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.259+2255A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472783 | |||||||
| chr4:100472892 | C | T | 1 | a0001c0001t0020g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259+2146G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472892 | |||||||
| chr4:100472919 | TATAG | T | 4 | a0002c0002t0001g0062 a0003c0003t0004g0158 a0003c0003t0035g0198 others(1): Show |
4 | HG02129.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+2115_259+2118d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100472919 | |||||||
| chr4:100473009 | T | TTA | 9 | a0001c0001t0002g0029 a0001c0001t0034g0140 a0002c0002t0001g0086 others(6): Show |
9 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.259+2027_259+2028d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473009 | |||||||
| chr4:100473012 | T | G | 1 | a0001c0001t0009g0121 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.259+2026A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473012 | |||||||
| chr4:100473015 | A | G | 1 | a0002c0002t0001g0054 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.259+2023T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473015 | |||||||
| chr4:100473019 | A | AT | 9 | a0001c0001t0002g0204 a0001c0001t0002g0222 a0001c0001t0002g0236 others(6): Show |
9 | HG00735.hp1 HG01099.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.259+2018dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473019 | |||||||
| chr4:100473021 | A | AT | 114 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(111): Show |
116 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.259+2016dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473021 | |||||||
| chr4:100473021 | A | T | 16 | a0001c0001t0002g0204 a0001c0001t0002g0222 a0001c0001t0002g0236 others(13): Show |
16 | HG00735.hp1 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.259+2017T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473021 | |||||||
| chr4:100473022 | T | TA | 45 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(42): Show |
46 | HG00639.hp1 HG00642.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.259+2015_259+2016i others(3): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473022 | |||||||
| chr4:100473023 | T | A | 11 | a0001c0001t0002g0122 a0001c0001t0003g0210 a0001c0001t0003g0255 others(8): Show |
11 | HG00735.hp2 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.259+2015A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473023 | |||||||
| chr4:100473024 | T | A | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.259+2014A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473024 | |||||||
| chr4:100473025 | T | A | 5 | a0001c0001t0002g0122 a0001c0001t0004g0154 a0001c0001t0004g0156 others(2): Show |
5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+2013A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473025 | |||||||
| chr4:100473054 | G | A | 16 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.259+1984C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473054 | |||||||
| chr4:100473168 | C | T | 9 | a0001c0001t0004g0004 a0001c0001t0004g0131 a0001c0001t0004g0250 others(6): Show |
10 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+1870G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473168 | |||||||
| chr4:100473365 | G | GTTTT | 12 | a0002c0002t0001g0002 a0002c0002t0001g0050 a0002c0002t0001g0051 others(9): Show |
13 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.259+1669_259+1672d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | |||||||
| chr4:100473365 | G | GTTTTT | 17 | a0001c0001t0001g0196 a0001c0001t0002g0032 a0002c0002t0001g0017 others(14): Show |
17 | HG00408.hp2 HG01074.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.259+1668_259+1672d others(7): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | |||||||
| chr4:100473365 | G | GTTTTTT | 17 | a0001c0001t0001g0195 a0001c0001t0002g0024 a0001c0001t0002g0028 others(14): Show |
17 | HG00639.hp2 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.259+1667_259+1672d others(8): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | |||||||
| chr4:100473365 | G | GTTTTTTT | 12 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(9): Show |
12 | HG00408.hp1 HG00738.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.259+1666_259+1672d others(9): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | |||||||
| chr4:100473365 | G | GTTTTTTT others(1): Show |
10 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0034 others(7): Show |
10 | HG00642.hp2 HG01069.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.259+1672_259+1673i others(10): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | |||||||
| chr4:100473365 | G | GTTTTTTT others(2): Show |
6 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0033 others(3): Show |
7 | HG00741.hp2 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.259+1672_259+1673i others(11): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | |||||||
| chr4:100473365 | G | GTTTTTTT others(3): Show |
3 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0023g0005 |
3 | HG02027.hp1 HG03927.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.259+1672_259+1673i others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | |||||||
| chr4:100473365 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0002g0015 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.259+1672_259+1673i others(13): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | |||||||
| chr4:100473365 | G | GTTTTTTT others(5): Show |
2 | a0001c0001t0002g0014 a0001c0001t0013g0008 |
2 | HG03492.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.259+1672_259+1673i others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | |||||||
| chr4:100473365 | G | GTTTTTTT others(6): Show |
1 | a0002c0002t0001g0016 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.259+1672_259+1673i others(15): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | |||||||
| chr4:100473365 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.259+1663_259+1672d others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | |||||||
| chr4:100473365 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0002g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.259+1662_259+1672d others(13): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | |||||||
| chr4:100473365 | GTTTTTTT others(5): Show |
G | 2 | a0002c0002t0001g0054 a0002c0002t0001g0055 |
2 | NA19058.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.259+1661_259+1672d others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | |||||||
| chr4:100473365 | GTTTTTTT others(6): Show |
G | 12 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0004g0162 others(9): Show |
12 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.259+1660_259+1672d others(15): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473365 | |||||||
| chr4:100473373 | G | GT | 31 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(28): Show |
31 | HG00639.hp1 HG00673.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.259+1664dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473373 | |||||||
| chr4:100473373 | G | GTT | 50 | a0001c0001t0001g0182 a0001c0001t0002g0003 a0001c0001t0002g0122 others(47): Show |
51 | HG00597.hp1 HG00673.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.259+1663_259+1664d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473373 | |||||||
| chr4:100473373 | G | GTTT | 24 | a0001c0001t0002g0127 a0001c0001t0002g0129 a0001c0001t0002g0181 others(21): Show |
24 | HG00597.hp2 HG01123.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.259+1662_259+1664d others(5): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473373 | |||||||
| chr4:100473373 | G | T | 85 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(82): Show |
87 | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.259+1665C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473373 | |||||||
| chr4:100473374 | TTTTTTTT others(5): Show |
T | 6 | a0001c0001t0004g0004 a0001c0001t0004g0131 a0001c0001t0004g0250 others(3): Show |
7 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.259+1652_259+1663d others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473374 | |||||||
| chr4:100473375 | TTTTTTTT others(4): Show |
T | 3 | a0001c0004t0004g0248 a0001c0004t0004g0249 a0002c0006t0004g0048 |
3 | HG02257.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.259+1652_259+1662d others(13): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473375 | |||||||
| chr4:100473381 | T | TG | 3 | a0001c0001t0005g0256 a0004c0005t0017g0019 a0004c0005t0017g0020 |
3 | HG00735.hp1 HG01515.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.259+1656_259+1657i others(3): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473381 | |||||||
| chr4:100473386 | G | T | 183 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(180): Show |
186 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(183): Show |
intron_variant | MODIFIER | c.259+1652C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473386 | |||||||
| chr4:100473499 | C | T | 3 | a0001c0001t0009g0121 a0001c0001t0009g0242 a0001c0001t0009g0243 |
3 | HG02559.hp2 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.259+1539G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473499 | |||||||
| chr4:100473559 | C | T | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259+1479G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473559 | |||||||
| chr4:100473599 | A | G | 30 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(27): Show |
31 | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.259+1439T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473599 | |||||||
| chr4:100473729 | T | C | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259+1309A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473729 | |||||||
| chr4:100473812 | CGAAAATT others(18): Show |
C | 2 | a0001c0001t0013g0246 a0001c0001t0027g0247 |
2 | HG00741.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.259+1201_259+1225d others(27): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473812 | |||||||
| chr4:100473820 | A | T | 1 | a0001c0001t0002g0228 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.259+1218T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473820 | |||||||
| chr4:100473837 | A | C | 2 | a0001c0001t0002g0127 a0001c0001t0002g0129 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.259+1201T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100473837 | |||||||
| chr4:100474005 | T | C | 89 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(86): Show |
90 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.259+1033A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474005 | |||||||
| chr4:100474019 | A | C | 1 | a0003c0003t0035g0198 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.259+1019T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474019 | |||||||
| chr4:100474058 | T | C | 10 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0004g0162 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.259+980A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474058 | |||||||
| chr4:100474487 | C | T | 2 | a0003c0003t0004g0158 a0003c0003t0035g0198 |
2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.259+551G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474487 | |||||||
| chr4:100474513 | A | C | 6 | a0002c0002t0001g0088 a0002c0002t0001g0093 a0002c0002t0001g0094 others(3): Show |
6 | HG00597.hp2 HG01361.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+525T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474513 | |||||||
| chr4:100474556 | T | C | 5 | a0001c0001t0008g0116 a0001c0001t0008g0117 a0001c0001t0008g0118 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+482A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474556 | |||||||
| chr4:100474601 | G | A | 5 | a0001c0001t0008g0116 a0001c0001t0008g0117 a0001c0001t0008g0118 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+437C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474601 | |||||||
| chr4:100474763 | T | G | 6 | a0001c0001t0002g0021 a0001c0001t0002g0037 a0001c0001t0002g0038 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+275A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474763 | |||||||
| chr4:100474829 | A | G | 137 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(134): Show |
140 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.259+209T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474829 | |||||||
| chr4:100474834 | G | A | 18 | a0001c0001t0003g0207 a0001c0001t0003g0255 a0001c0001t0005g0173 others(15): Show |
18 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.259+204C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474834 | |||||||
| chr4:100474954 | G | A | 1 | a0002c0002t0009g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.259+84C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 3/11 | chr4 | 100474954 | |||||||
| chr4:100475195 | G | A | 89 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(86): Show |
90 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.188-86C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475195 | |||||||
| chr4:100475244 | G | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.188-135C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475244 | |||||||
| chr4:100475302 | T | TAC | 9 | a0001c0001t0003g0220 a0001c0001t0003g0235 a0001c0001t0005g0202 others(6): Show |
9 | HG01934.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-195_188-194dup others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | |||||||
| chr4:100475302 | T | TACAC | 11 | a0001c0001t0002g0122 a0001c0001t0006g0006 a0001c0001t0006g0128 others(8): Show |
11 | HG00673.hp1 HG00735.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.188-197_188-194dup others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | |||||||
| chr4:100475302 | T | TACACAC | 24 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(21): Show |
24 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.188-199_188-194dup others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | |||||||
| chr4:100475302 | T | TACACACA others(1): Show |
33 | a0001c0001t0002g0007 a0001c0001t0002g0021 a0001c0001t0002g0024 others(30): Show |
34 | HG00639.hp2 HG01081.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.188-201_188-194dup others(8): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | |||||||
| chr4:100475302 | T | TACACACA others(3): Show |
91 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0002g0003 others(88): Show |
93 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.188-203_188-194dup others(10): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | |||||||
| chr4:100475302 | T | TACACACA others(5): Show |
16 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0182 others(13): Show |
17 | HG00408.hp1 HG00673.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.188-205_188-194dup others(12): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | |||||||
| chr4:100475302 | T | TACACACA others(7): Show |
11 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0230 others(8): Show |
11 | HG00741.hp2 HG01074.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.188-207_188-194dup others(14): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | |||||||
| chr4:100475302 | T | TACACACA others(9): Show |
6 | a0001c0001t0008g0116 a0001c0001t0008g0117 a0001c0001t0008g0118 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-209_188-194dup others(16): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | |||||||
| chr4:100475302 | TAC | T | 3 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 |
3 | HG03041.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.188-195_188-194del others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475302 | |||||||
| chr4:100475472 | C | T | 11 | a0001c0001t0004g0004 a0001c0001t0004g0131 a0001c0001t0004g0250 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.188-363G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475472 | |||||||
| chr4:100475512 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.188-403A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475512 | |||||||
| chr4:100475534 | T | C | 120 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(117): Show |
122 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.188-425A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475534 | |||||||
| chr4:100475658 | CCTTTTTT others(1): Show |
C | 24 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(21): Show |
25 | HG00741.hp2 HG01074.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.188-557_188-550del others(8): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475658 | |||||||
| chr4:100475658 | CCTTTTTT others(2): Show |
C | 94 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(91): Show |
95 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.188-558_188-550del others(9): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475658 | |||||||
| chr4:100475658 | CCTTTTTT others(3): Show |
C | 17 | a0001c0001t0002g0035 a0001c0001t0002g0122 a0001c0001t0004g0004 others(14): Show |
18 | HG00735.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.188-559_188-550del others(10): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475658 | |||||||
| chr4:100475659 | C | CT | 6 | a0001c0001t0003g0255 a0001c0001t0005g0174 a0001c0001t0005g0189 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-551dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | |||||||
| chr4:100475659 | C | CTT | 5 | a0001c0001t0001g0101 a0001c0001t0005g0173 a0001c0001t0005g0183 others(2): Show |
5 | HG02976.hp2 HG03139.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-552_188-551dup others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | |||||||
| chr4:100475659 | CT | C | 11 | a0001c0001t0002g0213 a0001c0001t0002g0217 a0001c0001t0003g0102 others(8): Show |
11 | HG00642.hp1 HG00642.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.188-551delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | |||||||
| chr4:100475659 | CTT | C | 6 | a0001c0001t0002g0187 a0001c0001t0003g0216 a0001c0001t0003g0218 others(3): Show |
6 | HG01516.hp1 HG01934.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-552_188-551del others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | |||||||
| chr4:100475659 | CTTTT | C | 13 | a0001c0001t0011g0112 a0001c0001t0011g0113 a0001c0001t0011g0114 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.188-554_188-551del others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | |||||||
| chr4:100475659 | CTTTTT | C | 8 | a0001c0001t0002g0178 a0001c0001t0002g0181 a0001c0001t0002g0224 others(5): Show |
8 | HG00597.hp1 HG00741.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-555_188-551del others(5): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | |||||||
| chr4:100475659 | CTTTTTT | C | 34 | a0001c0001t0001g0182 a0001c0001t0002g0003 a0001c0001t0002g0127 others(31): Show |
35 | HG00673.hp2 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.188-556_188-551del others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | |||||||
| chr4:100475659 | CTTTTTTT | C | 18 | a0001c0001t0002g0194 a0001c0001t0006g0128 a0001c0001t0006g0132 others(15): Show |
18 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.188-557_188-551del others(7): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | |||||||
| chr4:100475659 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0003g0210 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.188-566_188-551del others(16): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475659 | |||||||
| chr4:100475666 | T | A | 2 | a0001c0001t0004g0018 a0001c0001t0020g0023 |
2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.188-557A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475666 | |||||||
| chr4:100475666 | T | G | 7 | a0001c0001t0002g0178 a0001c0001t0002g0181 a0001c0001t0002g0224 others(4): Show |
7 | HG00597.hp1 HG00741.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-557A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475666 | |||||||
| chr4:100475667 | T | A | 24 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(21): Show |
25 | HG00741.hp2 HG01074.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.188-558A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475667 | |||||||
| chr4:100475667 | T | G | 34 | a0001c0001t0001g0182 a0001c0001t0002g0003 a0001c0001t0002g0127 others(31): Show |
35 | HG00673.hp2 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.188-558A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475667 | |||||||
| chr4:100475668 | T | A | 94 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 others(91): Show |
95 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.188-559A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475668 | |||||||
| chr4:100475668 | T | G | 16 | a0001c0001t0002g0194 a0001c0001t0006g0128 a0001c0001t0006g0132 others(13): Show |
16 | HG00639.hp1 HG00673.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.188-559A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475668 | |||||||
| chr4:100475669 | T | A | 17 | a0001c0001t0002g0035 a0001c0001t0002g0122 a0001c0001t0004g0004 others(14): Show |
18 | HG00735.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.188-560A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475669 | |||||||
| chr4:100475669 | T | G | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.188-560A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475669 | |||||||
| chr4:100475676 | T | G | 2 | a0001c0001t0002g0184 a0001c0001t0002g0232 |
2 | HG03831.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.188-567A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475676 | |||||||
| chr4:100475956 | GAGCCACT others(6): Show |
G | 6 | a0001c0001t0004g0004 a0001c0001t0004g0131 a0001c0001t0004g0250 others(3): Show |
7 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-860_188-848del others(13): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100475956 | |||||||
| chr4:100476162 | TCTCC | T | 21 | a0001c0001t0002g0122 a0001c0001t0003g0212 a0001c0001t0004g0154 others(18): Show |
21 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.188-1057_188-1054d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476162 | |||||||
| chr4:100476241 | CTTTCCTT others(9): Show |
C | 1 | a0001c0001t0002g0233 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.188-1148_188-1133d others(18): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476241 | |||||||
| chr4:100476687 | A | G | 64 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(61): Show |
66 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.188-1578T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476687 | |||||||
| chr4:100476721 | C | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(61): Show |
66 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.188-1612G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476721 | |||||||
| chr4:100476824 | A | G | 64 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(61): Show |
66 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.188-1715T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476824 | |||||||
| chr4:100476869 | G | A | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.188-1760C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476869 | |||||||
| chr4:100476878 | G | C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(61): Show |
66 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.188-1769C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476878 | |||||||
| chr4:100476922 | C | G | 43 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(40): Show |
44 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.188-1813G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476922 | |||||||
| chr4:100476949 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.188-1840A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476949 | |||||||
| chr4:100476986 | C | G | 1 | a0001c0001t0038g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.188-1877G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100476986 | |||||||
| chr4:100477024 | G | A | 9 | a0001c0001t0004g0004 a0001c0001t0004g0131 a0001c0001t0004g0250 others(6): Show |
10 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.188-1915C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477024 | |||||||
| chr4:100477029 | A | G | 1 | a0001c0001t0003g0210 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.188-1920T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477029 | |||||||
| chr4:100477048 | T | G | 64 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(61): Show |
66 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.188-1939A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477048 | |||||||
| chr4:100477220 | T | C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(61): Show |
66 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.188-2111A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477220 | |||||||
| chr4:100477261 | TAAAA | T | 64 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(61): Show |
66 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.188-2156_188-2153d others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477261 | |||||||
| chr4:100477365 | C | CT | 64 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(61): Show |
66 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.188-2257dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477365 | |||||||
| chr4:100477793 | CT | C | 71 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(68): Show |
73 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.187+2123delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477793 | |||||||
| chr4:100477849 | G | A | 64 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(61): Show |
66 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.187+2068C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477849 | |||||||
| chr4:100477882 | G | C | 151 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(148): Show |
154 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(151): Show |
intron_variant | MODIFIER | c.187+2035C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477882 | |||||||
| chr4:100477944 | A | C | 1 | a0001c0001t0005g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.187+1973T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477944 | |||||||
| chr4:100477969 | A | G | 10 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0004g0162 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.187+1948T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100477969 | |||||||
| chr4:100478078 | G | T | 9 | a0001c0001t0004g0004 a0001c0001t0004g0131 a0001c0001t0004g0250 others(6): Show |
10 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.187+1839C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478078 | |||||||
| chr4:100478124 | C | T | 1 | a0001c0001t0006g0006 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.187+1793G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478124 | |||||||
| chr4:100478127 | A | G | 64 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(61): Show |
66 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.187+1790T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478127 | |||||||
| chr4:100478156 | C | T | 63 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(60): Show |
65 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.187+1761G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478156 | |||||||
| chr4:100478348 | C | T | 5 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(2): Show |
5 | HG02486.hp2 HG02896.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+1569G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478348 | |||||||
| chr4:100478502 | T | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.187+1415A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478502 | |||||||
| chr4:100478546 | G | C | 1 | a0001c0001t0002g0003 | 2 | NA19001.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.187+1371C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478546 | |||||||
| chr4:100478660 | A | G | 5 | a0001c0001t0002g0122 a0001c0001t0004g0154 a0001c0001t0004g0156 others(2): Show |
5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+1257T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478660 | |||||||
| chr4:100478663 | C | T | 1 | a0002c0002t0001g0075 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.187+1254G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100478663 | |||||||
| chr4:100479078 | C | A | 3 | a0001c0004t0004g0248 a0001c0004t0004g0249 a0002c0006t0004g0048 |
3 | HG02257.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.187+839G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479078 | |||||||
| chr4:100479139 | G | A | 1 | a0001c0001t0007g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.187+778C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479139 | |||||||
| chr4:100479268 | T | A | 5 | a0001c0001t0002g0127 a0001c0001t0002g0129 a0001c0001t0006g0142 others(2): Show |
5 | HG00639.hp1 HG01255.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+649A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479268 | |||||||
| chr4:100479271 | G | GTTTTTC | 87 | a0002c0002t0001g0002 a0002c0002t0001g0016 a0002c0002t0001g0017 others(84): Show |
88 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(85): Show |
intron_variant | MODIFIER | c.187+645_187+646ins others(6): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479271 | |||||||
| chr4:100479348 | T | C | 2 | a0001c0001t0002g0021 a0001c0001t0002g0041 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.187+569A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479348 | |||||||
| chr4:100479564 | C | T | 4 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(1): Show |
4 | HG01975.hp1 HG02922.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+353G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479564 | |||||||
| chr4:100479633 | C | A | 1 | a0001c0001t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.187+284G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479633 | |||||||
| chr4:100479681 | A | G | 2 | a0001c0001t0002g0027 a0001c0001t0002g0028 |
2 | HG01081.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.187+236T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479681 | |||||||
| chr4:100479762 | C | A | 1 | a0001c0001t0012g0026 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.187+155G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479762 | |||||||
| chr4:100479845 | A | G | 76 | a0002c0002t0001g0002 a0002c0002t0001g0016 a0002c0002t0001g0017 others(73): Show |
77 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(74): Show |
intron_variant | MODIFIER | c.187+72T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479845 | |||||||
| chr4:100479858 | T | C | 1 | a0001c0001t0006g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.187+59A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 2/11 | chr4 | 100479858 | |||||||
| chr4:100480338 | G | T | 144 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(141): Show |
147 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(144): Show |
intron_variant | MODIFIER | c.65-299C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100480338 | |||||||
| chr4:100480585 | CAT | C | 78 | a0002c0002t0001g0002 a0002c0002t0001g0016 a0002c0002t0001g0017 others(75): Show |
79 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.65-548_65-547delAT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100480585 | |||||||
| chr4:100480710 | C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65-671G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100480710 | |||||||
| chr4:100481064 | T | C | 10 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0004g0162 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-1025A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481064 | |||||||
| chr4:100481083 | G | A | 1 | a0002c0002t0001g0100 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.65-1044C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481083 | |||||||
| chr4:100481145 | G | A | 2 | a0001c0001t0011g0109 a0001c0001t0011g0113 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.65-1106C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481145 | |||||||
| chr4:100481241 | C | G | 76 | a0002c0002t0001g0002 a0002c0002t0001g0016 a0002c0002t0001g0017 others(73): Show |
77 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(74): Show |
intron_variant | MODIFIER | c.65-1202G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481241 | |||||||
| chr4:100481344 | T | C | 174 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(171): Show |
177 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(174): Show |
intron_variant | MODIFIER | c.65-1305A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481344 | |||||||
| chr4:100481381 | G | C | 55 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(52): Show |
56 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.65-1342C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481381 | |||||||
| chr4:100481413 | A | G | 12 | a0001c0001t0002g0122 a0001c0001t0004g0154 a0001c0001t0004g0156 others(9): Show |
12 | HG00735.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.65-1374T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481413 | |||||||
| chr4:100481492 | C | T | 1 | a0002c0002t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.65-1453G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481492 | |||||||
| chr4:100481673 | A | G | 75 | a0002c0002t0001g0002 a0002c0002t0001g0016 a0002c0002t0001g0017 others(72): Show |
76 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.65-1634T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481673 | |||||||
| chr4:100481764 | C | G | 8 | a0001c0001t0004g0004 a0001c0001t0004g0131 a0001c0001t0004g0250 others(5): Show |
9 | HG01109.hp2 HG01891.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-1725G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481764 | |||||||
| chr4:100481828 | G | A | 14 | a0001c0001t0002g0122 a0001c0001t0004g0004 a0001c0001t0004g0131 others(11): Show |
15 | HG00735.hp2 HG01109.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.65-1789C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481828 | |||||||
| chr4:100481856 | T | A | 1 | a0001c0001t0003g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.65-1817A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100481856 | |||||||
| chr4:100482049 | T | C | 1 | a0001c0001t0002g0236 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.65-2010A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482049 | |||||||
| chr4:100482120 | A | G | 2 | a0001c0001t0015g0022 a0001c0001t0015g0115 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.65-2081T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482120 | |||||||
| chr4:100482304 | T | G | 67 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(64): Show |
69 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.65-2265A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482304 | |||||||
| chr4:100482310 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.65-2271A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482310 | |||||||
| chr4:100482319 | T | C | 5 | a0001c0001t0002g0122 a0001c0001t0004g0154 a0001c0001t0004g0156 others(2): Show |
5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-2280A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482319 | |||||||
| chr4:100482440 | A | G | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.65-2401T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482440 | |||||||
| chr4:100482459 | T | C | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.65-2420A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482459 | |||||||
| chr4:100482620 | T | C | 1 | a0001c0001t0004g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.65-2581A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482620 | |||||||
| chr4:100482625 | C | T | 1 | a0001c0001t0005g0244 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.65-2586G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482625 | |||||||
| chr4:100482744 | C | T | 2 | a0004c0005t0017g0019 a0004c0005t0017g0020 |
2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.65-2705G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482744 | |||||||
| chr4:100482880 | C | T | 1 | a0001c0001t0004g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.65-2841G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482880 | |||||||
| chr4:100482907 | A | G | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65-2868T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100482907 | |||||||
| chr4:100483033 | A | G | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | NA18973.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.65-2994T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100483033 | |||||||
| chr4:100483437 | C | T | 5 | a0001c0001t0008g0116 a0001c0001t0008g0117 a0001c0001t0008g0118 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-3398G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100483437 | |||||||
| chr4:100483448 | C | T | 1 | a0001c0001t0005g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-3409G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100483448 | |||||||
| chr4:100483482 | T | G | 1 | a0001c0001t0011g0109 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.65-3443A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100483482 | |||||||
| chr4:100483593 | C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65-3554G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100483593 | |||||||
| chr4:100484243 | A | G | 1 | a0001c0001t0002g0007 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.65-4204T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100484243 | |||||||
| chr4:100484435 | A | G | 5 | a0001c0001t0008g0116 a0001c0001t0008g0117 a0001c0001t0008g0118 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-4396T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100484435 | |||||||
| chr4:100484478 | C | T | 3 | a0001c0001t0009g0121 a0001c0001t0009g0242 a0001c0001t0009g0243 |
3 | HG02559.hp2 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.65-4439G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100484478 | |||||||
| chr4:100484578 | T | C | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.65-4539A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100484578 | |||||||
| chr4:100484924 | T | C | 2 | a0002c0002t0001g0065 a0002c0002t0001g0081 |
2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.65-4885A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100484924 | |||||||
| chr4:100484961 | C | T | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 |
3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.65-4922G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100484961 | |||||||
| chr4:100485056 | A | T | 10 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0004g0162 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-5017T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485056 | |||||||
| chr4:100485262 | G | T | 75 | a0001c0001t0001g0101 a0001c0001t0003g0085 a0001c0001t0003g0102 others(72): Show |
76 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.65-5223C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485262 | |||||||
| chr4:100485308 | T | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-5269A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485308 | |||||||
| chr4:100485310 | T | A | 1 | a0001c0001t0013g0246 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.65-5271A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485310 | |||||||
| chr4:100485429 | C | T | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-5390G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485429 | |||||||
| chr4:100485752 | C | A | 126 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(123): Show |
128 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.65-5713G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485752 | |||||||
| chr4:100485774 | G | A | 1 | a0001c0001t0006g0006 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.65-5735C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485774 | |||||||
| chr4:100485889 | C | G | 5 | a0001c0001t0002g0122 a0001c0001t0004g0154 a0001c0001t0004g0156 others(2): Show |
5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-5850G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485889 | |||||||
| chr4:100485922 | A | C | 5 | a0001c0001t0002g0122 a0001c0001t0004g0154 a0001c0001t0004g0156 others(2): Show |
5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-5883T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100485922 | |||||||
| chr4:100486058 | A | G | 1 | a0002c0002t0006g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.65-6019T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100486058 | |||||||
| chr4:100486139 | G | A | 1 | a0001c0001t0004g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.65-6100C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100486139 | |||||||
| chr4:100486516 | G | GTT | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-6479_65-6478dup others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100486516 | |||||||
| chr4:100486624 | A | T | 10 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(7): Show |
11 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-6585T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100486624 | |||||||
| chr4:100486801 | C | A | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.65-6762G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100486801 | |||||||
| chr4:100486809 | G | T | 27 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(24): Show |
28 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.65-6770C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100486809 | |||||||
| chr4:100486882 | A | G | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 |
3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.65-6843T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100486882 | |||||||
| chr4:100487401 | G | T | 1 | a0002c0002t0001g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.65-7362C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100487401 | |||||||
| chr4:100487493 | A | C | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.65-7454T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100487493 | |||||||
| chr4:100487619 | T | G | 1 | a0001c0001t0002g0245 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.65-7580A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100487619 | |||||||
| chr4:100487621 | T | C | 1 | a0001c0001t0006g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.65-7582A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100487621 | |||||||
| chr4:100487649 | G | A | 30 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(27): Show |
31 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.65-7610C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100487649 | |||||||
| chr4:100487802 | C | T | 2 | a0002c0002t0016g0111 a0003c0003t0036g0160 |
2 | HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.65-7763G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100487802 | |||||||
| chr4:100488879 | T | A | 7 | a0001c0001t0004g0004 a0001c0001t0004g0250 a0001c0001t0004g0251 others(4): Show |
8 | HG01109.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-8840A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100488879 | |||||||
| chr4:100489013 | C | G | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65-8974G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489013 | |||||||
| chr4:100489069 | G | C | 30 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(27): Show |
31 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.65-9030C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489069 | |||||||
| chr4:100489233 | G | T | 73 | a0001c0001t0001g0101 a0001c0001t0003g0085 a0001c0001t0003g0102 others(70): Show |
74 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.65-9194C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489233 | |||||||
| chr4:100489252 | T | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-9213A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489252 | |||||||
| chr4:100489497 | A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-9458T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489497 | |||||||
| chr4:100489625 | A | G | 5 | a0001c0001t0002g0122 a0001c0001t0004g0154 a0001c0001t0004g0156 others(2): Show |
5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-9586T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489625 | |||||||
| chr4:100489749 | C | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65-9710G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489749 | |||||||
| chr4:100489797 | A | G | 3 | a0002c0002t0007g0163 a0002c0002t0007g0164 a0002c0002t0007g0165 |
3 | HG01070.hp1 HG01071.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.65-9758T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489797 | |||||||
| chr4:100489819 | C | T | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65-9780G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489819 | |||||||
| chr4:100489926 | G | C | 7 | a0002c0002t0001g0139 a0002c0002t0001g0144 a0002c0002t0001g0146 others(4): Show |
7 | HG01109.hp1 HG01123.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-9887C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100489926 | |||||||
| chr4:100490174 | T | TA | 127 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(124): Show |
129 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.65-10136dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100490174 | |||||||
| chr4:100490178 | A | G | 5 | a0001c0001t0002g0122 a0001c0001t0004g0154 a0001c0001t0004g0156 others(2): Show |
5 | HG00735.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-10139T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100490178 | |||||||
| chr4:100490249 | C | A | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.65-10210G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100490249 | |||||||
| chr4:100490393 | C | A | 1 | a0001c0001t0012g0180 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.65-10354G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100490393 | |||||||
| chr4:100490750 | G | T | 128 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(125): Show |
130 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.65-10711C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100490750 | |||||||
| chr4:100490922 | T | C | 7 | a0001c0001t0004g0004 a0001c0001t0004g0250 a0001c0001t0004g0251 others(4): Show |
8 | HG01109.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-10883A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100490922 | |||||||
| chr4:100491048 | T | G | 1 | a0002c0002t0001g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.65-11009A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491048 | |||||||
| chr4:100491241 | C | A | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.65-11202G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491241 | |||||||
| chr4:100491245 | A | G | 1 | a0002c0002t0031g0138 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.65-11206T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491245 | |||||||
| chr4:100491261 | T | C | 1 | a0002c0002t0001g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.65-11222A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491261 | |||||||
| chr4:100491316 | G | A | 1 | a0001c0001t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-11277C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491316 | |||||||
| chr4:100491541 | A | G | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.65-11502T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491541 | |||||||
| chr4:100491765 | C | G | 5 | a0001c0001t0008g0116 a0001c0001t0008g0117 a0001c0001t0008g0118 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-11726G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491765 | |||||||
| chr4:100491857 | C | A | 27 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(24): Show |
28 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.65-11818G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491857 | |||||||
| chr4:100491884 | T | G | 70 | a0001c0001t0001g0101 a0001c0001t0003g0085 a0001c0001t0003g0102 others(67): Show |
71 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.65-11845A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491884 | |||||||
| chr4:100491983 | G | A | 22 | a0001c0001t0006g0006 a0001c0001t0006g0128 a0001c0001t0006g0133 others(19): Show |
22 | HG00639.hp1 HG00673.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.65-11944C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100491983 | |||||||
| chr4:100492103 | G | A | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.65-12064C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492103 | |||||||
| chr4:100492118 | A | G | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.65-12079T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492118 | |||||||
| chr4:100492385 | G | C | 3 | a0001c0001t0015g0022 a0001c0001t0015g0115 a0001c0001t0020g0023 |
3 | HG03225.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.65-12346C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492385 | |||||||
| chr4:100492426 | C | T | 10 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0004g0162 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-12387G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492426 | |||||||
| chr4:100492453 | A | G | 1 | a0001c0001t0011g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.65-12414T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492453 | |||||||
| chr4:100492510 | C | G | 1 | a0001c0001t0003g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-12471G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492510 | |||||||
| chr4:100492672 | ACAT | A | 5 | a0001c0001t0004g0004 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-12636_65-12634d others(5): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492672 | |||||||
| chr4:100492845 | C | T | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.65-12806G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100492845 | |||||||
| chr4:100493123 | G | A | 1 | a0001c0001t0012g0238 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.65-13084C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493123 | |||||||
| chr4:100493217 | C | T | 7 | a0001c0001t0004g0004 a0001c0001t0004g0250 a0001c0001t0004g0251 others(4): Show |
8 | HG01109.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-13178G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493217 | |||||||
| chr4:100493241 | G | A | 3 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0002g0241 |
3 | HG01257.hp1 HG01346.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.65-13202C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493241 | |||||||
| chr4:100493410 | G | A | 2 | a0001c0008t0005g0197 a0002c0002t0001g0066 |
2 | HG02056.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.65-13371C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493410 | |||||||
| chr4:100493554 | A | T | 1 | a0001c0001t0007g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.65-13515T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493554 | |||||||
| chr4:100493599 | CTTCTA | C | 3 | a0002c0002t0001g0135 a0002c0002t0001g0136 a0002c0002t0014g0137 |
3 | NA18980.hp2 NA19060.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.65-13565_65-13561d others(7): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493599 | |||||||
| chr4:100493684 | C | G | 1 | a0001c0008t0005g0197 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.65-13645G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493684 | |||||||
| chr4:100493763 | C | G | 1 | a0001c0001t0003g0206 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.65-13724G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493763 | |||||||
| chr4:100493868 | C | T | 1 | a0002c0002t0001g0135 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.65-13829G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100493868 | |||||||
| chr4:100494120 | G | T | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 |
3 | HG01884.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.65-14081C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100494120 | |||||||
| chr4:100494272 | T | C | 134 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(131): Show |
137 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.65-14233A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100494272 | |||||||
| chr4:100494422 | G | T | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.65-14383C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100494422 | |||||||
| chr4:100494761 | C | T | 69 | a0001c0001t0001g0101 a0001c0001t0003g0085 a0001c0001t0003g0102 others(66): Show |
70 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.65-14722G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100494761 | |||||||
| chr4:100494787 | C | CT | 11 | a0001c0001t0002g0122 a0002c0002t0001g0169 a0002c0002t0001g0170 others(8): Show |
11 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-14749dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100494787 | |||||||
| chr4:100494947 | A | AT | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-14909dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100494947 | |||||||
| chr4:100495007 | T | A | 173 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(170): Show |
176 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(173): Show |
intron_variant | MODIFIER | c.65-14968A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100495007 | |||||||
| chr4:100495622 | G | A | 1 | a0001c0001t0011g0109 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.65-15583C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100495622 | |||||||
| chr4:100495648 | C | T | 1 | a0001c0001t0002g0007 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.65-15609G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100495648 | |||||||
| chr4:100495764 | A | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-15725T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100495764 | |||||||
| chr4:100495874 | T | C | 138 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(135): Show |
141 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(138): Show |
intron_variant | MODIFIER | c.65-15835A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100495874 | |||||||
| chr4:100496016 | C | T | 2 | a0002c0002t0001g0050 a0002c0002t0001g0051 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.65-15977G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100496016 | |||||||
| chr4:100496517 | C | G | 2 | a0001c0001t0028g0175 a0003c0003t0036g0160 |
2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.65-16478G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100496517 | |||||||
| chr4:100496604 | A | C | 2 | a0001c0001t0028g0175 a0003c0003t0036g0160 |
2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.65-16565T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100496604 | |||||||
| chr4:100497066 | G | A | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-17027C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497066 | |||||||
| chr4:100497113 | A | G | 1 | a0001c0001t0007g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.65-17074T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497113 | |||||||
| chr4:100497239 | T | C | 29 | a0001c0001t0002g0127 a0001c0001t0002g0129 a0001c0001t0004g0154 others(26): Show |
29 | HG00639.hp1 HG00673.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.65-17200A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497239 | |||||||
| chr4:100497246 | T | TAA | 8 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0004g0162 others(5): Show |
8 | HG02451.hp1 HG02717.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-17209_65-17208d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497246 | |||||||
| chr4:100497246 | TAA | T | 5 | a0001c0001t0004g0004 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-17209_65-17208d others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497246 | |||||||
| chr4:100497323 | A | G | 2 | a0001c0001t0028g0175 a0003c0003t0036g0160 |
2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.65-17284T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497323 | |||||||
| chr4:100497387 | T | G | 3 | a0001c0001t0002g0032 a0001c0001t0002g0245 a0001c0001t0005g0244 |
3 | HG02886.hp1 HG03490.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.65-17348A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497387 | |||||||
| chr4:100497416 | G | T | 2 | a0002c0002t0001g0016 a0002c0002t0001g0017 |
2 | NA18946.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.65-17377C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497416 | |||||||
| chr4:100497427 | A | G | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-17388T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497427 | |||||||
| chr4:100497435 | A | G | 134 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(131): Show |
137 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.65-17396T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497435 | |||||||
| chr4:100497520 | G | C | 124 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(121): Show |
126 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.65-17481C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497520 | |||||||
| chr4:100497668 | T | G | 134 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(131): Show |
137 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.65-17629A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497668 | |||||||
| chr4:100497829 | G | A | 3 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 |
4 | HG01257.hp2 HG01258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-17790C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100497829 | |||||||
| chr4:100498115 | G | A | 2 | a0001c0001t0006g0128 a0001c0001t0006g0149 |
2 | HG02056.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.65-18076C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100498115 | |||||||
| chr4:100498274 | A | G | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | NA18979.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.65-18235T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100498274 | |||||||
| chr4:100498303 | G | A | 7 | a0001c0001t0004g0004 a0001c0001t0004g0250 a0001c0001t0004g0251 others(4): Show |
8 | HG01109.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-18264C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100498303 | |||||||
| chr4:100498648 | G | T | 79 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(76): Show |
80 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.65-18609C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100498648 | |||||||
| chr4:100498732 | G | A | 5 | a0001c0001t0008g0116 a0001c0001t0008g0117 a0001c0001t0008g0118 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-18693C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100498732 | |||||||
| chr4:100499054 | G | A | 1 | a0001c0001t0008g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.64+18797C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100499054 | |||||||
| chr4:100499059 | AT | A | 5 | a0001c0001t0004g0004 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+18791delA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100499059 | |||||||
| chr4:100499336 | T | G | 2 | a0001c0001t0011g0109 a0001c0001t0011g0113 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.64+18515A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100499336 | |||||||
| chr4:100499374 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.64+18477T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100499374 | |||||||
| chr4:100499448 | C | A | 5 | a0001c0001t0004g0004 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+18403G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100499448 | |||||||
| chr4:100499811 | G | A | 1 | a0002c0002t0001g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.64+18040C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100499811 | |||||||
| chr4:100499998 | A | G | 1 | a0002c0002t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.64+17853T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100499998 | |||||||
| chr4:100500101 | T | TA | 7 | a0001c0001t0004g0004 a0001c0001t0004g0250 a0001c0001t0004g0251 others(4): Show |
8 | HG01109.hp2 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+17749dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500101 | |||||||
| chr4:100500150 | A | G | 2 | a0002c0002t0026g0049 a0002c0006t0004g0048 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64+17701T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500150 | |||||||
| chr4:100500303 | C | A | 1 | a0001c0001t0004g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.64+17548G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500303 | |||||||
| chr4:100500478 | T | C | 1 | a0002c0002t0016g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64+17373A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500478 | |||||||
| chr4:100500734 | A | G | 2 | a0001c0001t0006g0133 a0001c0001t0006g0134 |
2 | HG02735.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.64+17117T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500734 | |||||||
| chr4:100500794 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+17057T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500794 | |||||||
| chr4:100500892 | A | T | 133 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(130): Show |
136 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.64+16959T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500892 | |||||||
| chr4:100500967 | T | C | 11 | a0002c0002t0001g0002 a0002c0002t0001g0042 a0002c0002t0001g0046 others(8): Show |
12 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+16884A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100500967 | |||||||
| chr4:100501010 | T | G | 1 | a0001c0001t0008g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64+16841A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501010 | |||||||
| chr4:100501120 | G | A | 134 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(131): Show |
137 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.64+16731C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501120 | |||||||
| chr4:100501195 | G | C | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.64+16656C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501195 | |||||||
| chr4:100501386 | A | G | 14 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0183 others(11): Show |
14 | HG01070.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.64+16465T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501386 | |||||||
| chr4:100501572 | T | C | 23 | a0001c0001t0001g0101 a0001c0001t0003g0085 a0001c0001t0003g0102 others(20): Show |
23 | HG00597.hp2 HG01192.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.64+16279A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501572 | |||||||
| chr4:100501594 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.64+16257A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501594 | |||||||
| chr4:100501638 | T | C | 13 | a0002c0002t0001g0002 a0002c0002t0001g0042 a0002c0002t0001g0046 others(10): Show |
14 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.64+16213A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501638 | |||||||
| chr4:100501855 | G | GT | 32 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(29): Show |
33 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.64+15995dupA | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100501855 | |||||||
| chr4:100502007 | T | G | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+15844A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502007 | |||||||
| chr4:100502013 | G | A | 1 | a0001c0001t0003g0106 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.64+15838C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502013 | |||||||
| chr4:100502015 | C | T | 5 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0002g0193 others(2): Show |
5 | HG02027.hp1 NA18943.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+15836G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502015 | |||||||
| chr4:100502023 | A | G | 1 | a0002c0002t0003g0047 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.64+15828T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502023 | |||||||
| chr4:100502106 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64+15745C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502106 | |||||||
| chr4:100502162 | T | C | 2 | a0001c0001t0028g0175 a0003c0003t0036g0160 |
2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.64+15689A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502162 | |||||||
| chr4:100502169 | A | G | 134 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(131): Show |
137 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.64+15682T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502169 | |||||||
| chr4:100502256 | T | A | 3 | a0001c0001t0015g0022 a0001c0001t0015g0115 a0001c0001t0020g0023 |
3 | HG03225.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.64+15595A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502256 | |||||||
| chr4:100502861 | T | G | 3 | a0002c0002t0001g0075 a0002c0002t0001g0076 a0002c0002t0001g0077 |
3 | HG00408.hp2 NA19066.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.64+14990A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100502861 | |||||||
| chr4:100503231 | T | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+14620A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503231 | |||||||
| chr4:100503248 | C | T | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.64+14603G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503248 | |||||||
| chr4:100503327 | G | C | 1 | a0001c0001t0020g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64+14524C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503327 | |||||||
| chr4:100503336 | TTTGGCAT others(12): Show |
T | 6 | a0001c0001t0005g0183 a0001c0001t0005g0191 a0001c0001t0005g0192 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+14496_64+14514d others(21): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503336 | |||||||
| chr4:100503420 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+14431T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503420 | |||||||
| chr4:100503549 | T | C | 1 | a0004c0005t0017g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64+14302A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503549 | |||||||
| chr4:100503712 | A | G | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+14139T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503712 | |||||||
| chr4:100503827 | A | G | 4 | a0001c0001t0002g0187 a0001c0001t0003g0186 a0001c0001t0003g0188 others(1): Show |
4 | HG01258.hp2 HG01516.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+14024T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100503827 | |||||||
| chr4:100504076 | A | G | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0012g0026 |
3 | HG00738.hp1 HG01106.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.64+13775T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504076 | |||||||
| chr4:100504192 | A | G | 1 | a0001c0001t0003g0186 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.64+13659T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504192 | |||||||
| chr4:100504240 | G | A | 1 | a0001c0001t0027g0247 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.64+13611C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504240 | |||||||
| chr4:100504302 | A | C | 126 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(123): Show |
128 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.64+13549T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504302 | |||||||
| chr4:100504320 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64+13531C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504320 | |||||||
| chr4:100504352 | T | A | 1 | a0002c0002t0001g0150 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.64+13499A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504352 | |||||||
| chr4:100504422 | T | G | 29 | a0001c0001t0002g0127 a0001c0001t0002g0129 a0001c0001t0004g0154 others(26): Show |
29 | HG00639.hp1 HG00673.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.64+13429A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504422 | |||||||
| chr4:100504517 | C | A | 3 | a0002c0002t0001g0078 a0002c0002t0001g0079 a0002c0002t0001g0080 |
3 | HG02132.hp2 NA18984.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.64+13334G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504517 | |||||||
| chr4:100504579 | TAGG | T | 124 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(121): Show |
126 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.64+13269_64+13271d others(5): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504579 | |||||||
| chr4:100504721 | C | T | 124 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(121): Show |
126 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.64+13130G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504721 | |||||||
| chr4:100504877 | G | T | 1 | a0001c0001t0008g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64+12974C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504877 | |||||||
| chr4:100504940 | T | G | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+12911A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100504940 | |||||||
| chr4:100505108 | A | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0185 |
3 | HG00408.hp1 NA19012.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.64+12743T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505108 | |||||||
| chr4:100505197 | G | A | 4 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0178 others(1): Show |
4 | NA18747.hp2 NA18955.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+12654C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505197 | |||||||
| chr4:100505241 | G | C | 2 | a0001c0001t0013g0246 a0001c0001t0027g0247 |
2 | HG00741.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.64+12610C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505241 | |||||||
| chr4:100505310 | G | A | 33 | a0001c0001t0004g0131 a0001c0001t0004g0154 a0001c0001t0004g0156 others(30): Show |
33 | HG00639.hp1 HG00673.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.64+12541C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505310 | |||||||
| chr4:100505505 | C | T | 41 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(38): Show |
42 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.64+12346G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505505 | |||||||
| chr4:100505571 | C | A | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+12280G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505571 | |||||||
| chr4:100505575 | T | C | 1 | a0001c0001t0006g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.64+12276A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505575 | |||||||
| chr4:100505665 | T | C | 1 | a0003c0003t0036g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+12186A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505665 | |||||||
| chr4:100505693 | C | T | 1 | a0001c0001t0003g0085 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.64+12158G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505693 | |||||||
| chr4:100505701 | C | T | 2 | a0004c0005t0017g0019 a0004c0005t0017g0020 |
2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.64+12150G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505701 | |||||||
| chr4:100505732 | C | G | 39 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(36): Show |
40 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.64+12119G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505732 | |||||||
| chr4:100505804 | T | TA | 4 | a0001c0001t0011g0109 a0001c0001t0011g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+12046dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505804 | |||||||
| chr4:100505836 | C | T | 1 | a0002c0002t0001g0046 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64+12015G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100505836 | |||||||
| chr4:100506075 | A | T | 2 | a0001c0001t0028g0175 a0003c0003t0036g0160 |
2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.64+11776T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506075 | |||||||
| chr4:100506132 | A | G | 3 | a0001c0001t0015g0022 a0001c0001t0015g0115 a0001c0001t0020g0023 |
3 | HG03225.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.64+11719T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506132 | |||||||
| chr4:100506139 | A | C | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.64+11712T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506139 | |||||||
| chr4:100506255 | T | A | 1 | a0001c0001t0002g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64+11596A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506255 | |||||||
| chr4:100506384 | A | G | 2 | a0001c0004t0004g0248 a0001c0004t0004g0249 |
2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.64+11467T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506384 | |||||||
| chr4:100506414 | C | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.64+11437G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506414 | |||||||
| chr4:100506468 | T | C | 126 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(123): Show |
128 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.64+11383A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506468 | |||||||
| chr4:100506481 | G | A | 6 | a0001c0001t0008g0116 a0001c0001t0008g0117 a0001c0001t0008g0118 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+11370C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506481 | |||||||
| chr4:100506516 | G | A | 172 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(169): Show |
175 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(172): Show |
intron_variant | MODIFIER | c.64+11335C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506516 | |||||||
| chr4:100506531 | C | A | 2 | a0001c0001t0028g0175 a0003c0003t0036g0160 |
2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.64+11320G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506531 | |||||||
| chr4:100506548 | T | C | 5 | a0001c0001t0008g0116 a0001c0001t0008g0117 a0001c0001t0008g0118 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+11303A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506548 | |||||||
| chr4:100506671 | T | C | 126 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(123): Show |
128 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.64+11180A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506671 | |||||||
| chr4:100506820 | G | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.64+11031C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100506820 | |||||||
| chr4:100507056 | T | A | 6 | a0001c0001t0002g0021 a0001c0001t0002g0037 a0001c0001t0002g0038 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+10795A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100507056 | |||||||
| chr4:100507097 | T | A | 124 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(121): Show |
126 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.64+10754A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100507097 | |||||||
| chr4:100507657 | C | T | 1 | a0001c0001t0002g0184 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.64+10194G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100507657 | |||||||
| chr4:100507829 | C | T | 2 | a0001c0001t0005g0183 a0003c0003t0036g0160 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.64+10022G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100507829 | |||||||
| chr4:100507901 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+9950T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100507901 | |||||||
| chr4:100507910 | A | G | 10 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0004g0162 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+9941T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100507910 | |||||||
| chr4:100508232 | A | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG00408.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.64+9619T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100508232 | |||||||
| chr4:100508296 | T | A | 132 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(129): Show |
135 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.64+9555A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100508296 | |||||||
| chr4:100508451 | T | C | 132 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(129): Show |
135 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.64+9400A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100508451 | |||||||
| chr4:100508569 | A | G | 1 | a0002c0002t0001g0045 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.64+9282T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100508569 | |||||||
| chr4:100508797 | T | G | 1 | a0002c0002t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.64+9054A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100508797 | |||||||
| chr4:100508953 | G | C | 174 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(171): Show |
177 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(174): Show |
intron_variant | MODIFIER | c.64+8898C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100508953 | |||||||
| chr4:100509142 | A | T | 52 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(49): Show |
53 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.64+8709T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509142 | |||||||
| chr4:100509344 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+8507T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509344 | |||||||
| chr4:100509485 | A | G | 10 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0004g0162 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+8366T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509485 | |||||||
| chr4:100509488 | G | C | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+8363C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509488 | |||||||
| chr4:100509568 | T | C | 1 | a0001c0001t0006g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.64+8283A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509568 | |||||||
| chr4:100509589 | C | A | 10 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0004g0162 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+8262G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509589 | |||||||
| chr4:100509613 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64+8238G>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509613 | |||||||
| chr4:100509662 | A | C | 2 | a0002c0002t0016g0110 a0002c0002t0016g0111 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.64+8189T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509662 | |||||||
| chr4:100509697 | G | A | 1 | a0002c0002t0001g0107 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64+8154C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509697 | |||||||
| chr4:100509915 | T | TTAG | 127 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(124): Show |
129 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.64+7933_64+7935dup others(3): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100509915 | |||||||
| chr4:100510014 | T | G | 2 | a0002c0002t0003g0082 a0002c0002t0003g0083 |
2 | NA18984.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.64+7837A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100510014 | |||||||
| chr4:100510102 | T | G | 127 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(124): Show |
129 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.64+7749A>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100510102 | |||||||
| chr4:100510106 | G | C | 10 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0004g0162 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+7745C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100510106 | |||||||
| chr4:100510448 | G | A | 127 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(124): Show |
129 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.64+7403C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100510448 | |||||||
| chr4:100510575 | C | T | 1 | a0001c0001t0028g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.64+7276G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100510575 | |||||||
| chr4:100510787 | A | G | 3 | a0001c0001t0011g0109 a0001c0001t0011g0113 a0001c0001t0011g0114 |
3 | HG02486.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.64+7064T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100510787 | |||||||
| chr4:100510928 | G | A | 75 | a0001c0001t0001g0101 a0001c0001t0003g0085 a0001c0001t0003g0102 others(72): Show |
76 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.64+6923C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100510928 | |||||||
| chr4:100511032 | A | G | 127 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(124): Show |
129 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.64+6819T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511032 | |||||||
| chr4:100511057 | G | C | 1 | a0001c0001t0009g0121 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.64+6794C>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511057 | |||||||
| chr4:100511103 | C | T | 3 | a0001c0001t0015g0022 a0001c0001t0015g0115 a0001c0001t0020g0023 |
3 | HG03225.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.64+6748G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511103 | |||||||
| chr4:100511298 | A | G | 1 | a0001c0001t0011g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.64+6553T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511298 | |||||||
| chr4:100511384 | T | A | 5 | a0001c0001t0004g0154 a0001c0001t0004g0156 a0001c0001t0006g0157 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+6467A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511384 | |||||||
| chr4:100511488 | T | A | 127 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(124): Show |
129 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.64+6363A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511488 | |||||||
| chr4:100511537 | C | A | 1 | a0002c0002t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.64+6314G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511537 | |||||||
| chr4:100511672 | G | A | 10 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0004g0162 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+6179C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511672 | |||||||
| chr4:100511692 | G | T | 127 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(124): Show |
129 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.64+6159C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511692 | |||||||
| chr4:100511836 | T | TA | 133 | a0001c0001t0001g0101 a0001c0001t0002g0001 a0001c0001t0002g0007 others(130): Show |
136 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.64+6014dupT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511836 | |||||||
| chr4:100511985 | T | C | 1 | a0001c0001t0032g0254 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.64+5866A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511985 | |||||||
| chr4:100511999 | A | G | 1 | a0001c0001t0006g0006 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.64+5852T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100511999 | |||||||
| chr4:100512097 | G | A | 23 | a0001c0001t0001g0101 a0001c0001t0003g0085 a0001c0001t0003g0102 others(20): Show |
23 | HG00597.hp2 HG01192.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.64+5754C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512097 | |||||||
| chr4:100512139 | C | A | 1 | a0002c0002t0001g0107 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64+5712G>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512139 | |||||||
| chr4:100512178 | G | A | 33 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(30): Show |
34 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.64+5673C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512178 | |||||||
| chr4:100512186 | G | A | 1 | a0001c0001t0003g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+5665C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512186 | |||||||
| chr4:100512517 | A | T | 1 | a0001c0001t0006g0128 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.64+5334T>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512517 | |||||||
| chr4:100512622 | T | C | 1 | a0001c0001t0008g0120 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.64+5229A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512622 | |||||||
| chr4:100512750 | G | A | 75 | a0001c0001t0001g0101 a0001c0001t0003g0085 a0001c0001t0003g0102 others(72): Show |
76 | HG00408.hp2 HG00597.hp2 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.64+5101C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512750 | |||||||
| chr4:100512786 | A | G | 1 | a0001c0001t0002g0127 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.64+5065T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512786 | |||||||
| chr4:100512806 | CA | C | 5 | a0001c0001t0002g0021 a0001c0001t0002g0181 a0001c0001t0012g0180 others(2): Show |
5 | HG01070.hp1 HG01192.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+5044delT | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512806 | |||||||
| chr4:100512906 | T | C | 10 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0004g0162 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+4945A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100512906 | |||||||
| chr4:100513207 | G | A | 128 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(125): Show |
130 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.64+4644C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100513207 | |||||||
| chr4:100513584 | T | C | 1 | a0003c0003t0004g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64+4267A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100513584 | |||||||
| chr4:100513596 | A | C | 128 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(125): Show |
130 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.64+4255T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100513596 | |||||||
| chr4:100513613 | G | T | 1 | a0002c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.64+4238C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100513613 | |||||||
| chr4:100513755 | T | C | 1 | a0002c0002t0001g0108 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.64+4096A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100513755 | |||||||
| chr4:100513999 | T | C | 1 | a0001c0001t0011g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.64+3852A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100513999 | |||||||
| chr4:100514140 | C | T | 3 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 |
3 | HG01975.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.64+3711G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100514140 | |||||||
| chr4:100514224 | A | G | 129 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(126): Show |
131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.64+3627T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100514224 | |||||||
| chr4:100514236 | A | C | 13 | a0001c0001t0002g0122 a0001c0001t0028g0175 a0002c0002t0001g0169 others(10): Show |
13 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.64+3615T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100514236 | |||||||
| chr4:100514694 | T | C | 2 | a0001c0001t0005g0256 a0001c0001t0005g0257 |
2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.64+3157A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100514694 | |||||||
| chr4:100514955 | T | C | 129 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(126): Show |
131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.64+2896A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100514955 | |||||||
| chr4:100515044 | A | G | 71 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(68): Show |
72 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.64+2807T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100515044 | |||||||
| chr4:100515161 | G | T | 39 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(36): Show |
40 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.64+2690C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100515161 | |||||||
| chr4:100515309 | T | C | 1 | a0001c0001t0004g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64+2542A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100515309 | |||||||
| chr4:100515406 | G | A | 1 | a0001c0001t0011g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.64+2445C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100515406 | |||||||
| chr4:100515509 | G | A | 127 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(124): Show |
129 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.64+2342C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100515509 | |||||||
| chr4:100515701 | T | A | 1 | a0001c0001t0029g0159 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.64+2150A>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100515701 | |||||||
| chr4:100515835 | A | AAAAC | 12 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(9): Show |
13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.64+2012_64+2015dup others(4): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100515835 | |||||||
| chr4:100516003 | T | TG | 116 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(113): Show |
118 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.64+1847dupC | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516003 | |||||||
| chr4:100516097 | C | T | 4 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0178 others(1): Show |
4 | NA18747.hp2 NA18955.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+1754G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516097 | |||||||
| chr4:100516185 | G | T | 128 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(125): Show |
130 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.64+1666C>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516185 | |||||||
| chr4:100516208 | A | G | 38 | a0001c0001t0002g0127 a0001c0001t0002g0129 a0001c0001t0004g0131 others(35): Show |
38 | HG00639.hp1 HG00673.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.64+1643T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516208 | |||||||
| chr4:100516357 | A | G | 129 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(126): Show |
131 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.64+1494T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516357 | |||||||
| chr4:100516366 | C | T | 128 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(125): Show |
130 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.64+1485G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516366 | |||||||
| chr4:100516372 | T | C | 1 | a0001c0001t0003g0258 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.64+1479A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516372 | |||||||
| chr4:100516389 | G | GGA | 10 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0004g0162 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+1460_64+1461dup others(2): Show |
EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516389 | |||||||
| chr4:100516427 | T | C | 128 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(125): Show |
130 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.64+1424A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516427 | |||||||
| chr4:100516522 | A | G | 167 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(164): Show |
169 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(166): Show |
intron_variant | MODIFIER | c.64+1329T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516522 | |||||||
| chr4:100516693 | T | C | 1 | a0001c0001t0015g0115 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.64+1158A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516693 | |||||||
| chr4:100516735 | A | G | 2 | a0001c0001t0005g0173 a0001c0001t0005g0174 |
2 | HG02559.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.64+1116T>C | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516735 | |||||||
| chr4:100516829 | A | C | 1 | a0001c0001t0002g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64+1022T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516829 | |||||||
| chr4:100516863 | T | C | 5 | a0001c0001t0008g0116 a0001c0001t0008g0117 a0001c0001t0008g0118 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+988A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516863 | |||||||
| chr4:100516932 | C | T | 1 | a0003c0003t0002g0172 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.64+919G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100516932 | |||||||
| chr4:100517018 | G | A | 166 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(163): Show |
168 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(165): Show |
intron_variant | MODIFIER | c.64+833C>T | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100517018 | |||||||
| chr4:100517233 | T | C | 167 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(164): Show |
169 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(166): Show |
intron_variant | MODIFIER | c.64+618A>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100517233 | |||||||
| chr4:100517350 | C | T | 168 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(165): Show |
170 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.64+501G>A | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100517350 | |||||||
| chr4:100517417 | A | C | 117 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0101 others(114): Show |
119 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.64+434T>G | EMCN | ENSG00000164035.10 | transcript | ENST00000296420.9 | protein_coding | 1/11 | chr4 | 100517417 |