Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 129080 |
| ensemblid | ENSG00000186998.16 |
| hgncid | 18036 |
| symbol | EMID1 |
| name | EMI domain containing 1 |
| refseq_nuc | NM_133455.4 |
| refseq_prot | NP_597712.2 |
| ensembl_nuc | ENST00000334018.11 |
| ensembl_prot | ENSP00000335481.6 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 29205896 |
| end | 29259597 |
| strand | + |
| ver | v1.2 |
| region | chr22:29205896-29259597 |
| region5000 | chr22:29200896-29264597 |
| regionname0 | EMID1_chr22_29205896_29259597 |
| regionname5000 | EMID1_chr22_29200896_29264597 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 443 | 143 | 19 | 28 | 52 | 9 | 33 | 40 | EMID1_chr22_29200896_29264597 | EMID1 | MGGPR others(438): Show |
chr22 | 29200896 | 29264597 |
| a0002 | 0/0 | 443 | 144 | 55 | 13 | 65 | 1 | 10 | 47 | EMID1_chr22_29200896_29264597 | EMID1 | MGGPR others(438): Show |
chr22 | 29200896 | 29264597 |
| a0003 | 0/0 | 443 | 37 | 16 | 2 | 19 | 0 | 0 | 16 | EMID1_chr22_29200896_29264597 | EMID1 | MGGPR others(438): Show |
chr22 | 29200896 | 29264597 |
| a0004 | 0/0 | 443 | 22 | 3 | 7 | 12 | 0 | 0 | 11 | EMID1_chr22_29200896_29264597 | EMID1 | MGGPR others(438): Show |
chr22 | 29200896 | 29264597 |
| a0005 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | MGGPR others(438): Show |
chr22 | 29200896 | 29264597 |
| a0006 | 0/0 | 443 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | MGGPR others(438): Show |
chr22 | 29200896 | 29264597 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1329 | 142 | 19 | 28 | 52 | 9 | 32 | EMID1_chr22_29200896_29264597 | EMID1 | ATGGG others(1324): Show |
chr22 | 29200896 | 29264597 | ||
| a0001c0005 | 0/0 | 1329 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | ATGGG others(1324): Show |
chr22 | 29200896 | 29264597 | ||
| a0002c0002 | 0/0 | 1329 | 142 | 53 | 13 | 65 | 1 | 10 | EMID1_chr22_29200896_29264597 | EMID1 | ATGGG others(1324): Show |
chr22 | 29200896 | 29264597 | ||
| a0002c0008 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | ATGGG others(1324): Show |
chr22 | 29200896 | 29264597 | ||
| a0002c0009 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | ATGGG others(1324): Show |
chr22 | 29200896 | 29264597 | ||
| a0003c0003 | 0/0 | 1329 | 37 | 16 | 2 | 19 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | ATGGG others(1324): Show |
chr22 | 29200896 | 29264597 | ||
| a0004c0004 | 0/0 | 1329 | 22 | 3 | 7 | 12 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | ATGGG others(1324): Show |
chr22 | 29200896 | 29264597 | ||
| a0005c0007 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | ATGGG others(1324): Show |
chr22 | 29200896 | 29264597 | ||
| a0006c0006 | 0/0 | 1329 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | ATGGG others(1324): Show |
chr22 | 29200896 | 29264597 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2128 | 79 | 4 | 20 | 27 | 5 | 22 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0001c0001t0002 | 0/0 | 2128 | 33 | 9 | 7 | 8 | 2 | 7 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0001c0001t0003 | 1/0 | 2128 | 24 | 5 | 1 | 14 | 2 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0001c0001t0007 | 0/0 | 2128 | 2 | 0 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0001c0001t0008 | 0/0 | 2128 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0001c0001t0009 | 0/0 | 2128 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0001c0001t0010 | 0/0 | 2128 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0001c0001t0012 | 0/0 | 2128 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0001c0005t0001 | 0/0 | 2128 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0002c0002t0001 | 0/0 | 2128 | 53 | 19 | 5 | 21 | 0 | 8 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0002c0002t0002 | 0/0 | 2128 | 63 | 23 | 7 | 31 | 1 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0002c0002t0003 | 0/0 | 2128 | 17 | 2 | 1 | 13 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0002c0002t0004 | 0/0 | 2128 | 6 | 6 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0002c0002t0006 | 0/0 | 2128 | 2 | 2 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0002c0002t0011 | 0/0 | 2128 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0002c0008t0002 | 0/0 | 2128 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0002c0009t0001 | 0/0 | 2128 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0003c0003t0001 | 0/0 | 2128 | 9 | 6 | 2 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0003c0003t0002 | 0/0 | 2128 | 4 | 2 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0003c0003t0003 | 0/0 | 2128 | 20 | 4 | 0 | 16 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0003c0003t0005 | 0/0 | 2128 | 4 | 4 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0004c0004t0001 | 0/0 | 2128 | 2 | 0 | 2 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0004c0004t0002 | 0/0 | 2128 | 3 | 1 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0004c0004t0003 | 0/0 | 2128 | 17 | 2 | 5 | 10 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0005c0007t0003 | 0/0 | 2128 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| a0006c0006t0003 | 0/0 | 2128 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | GCCTC others(2123): Show |
chr22 | 29200896 | 29264597 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0025 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0268 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0009g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0010g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0001t0012g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0001c0005t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0003g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0002t0011g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0008t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0002c0009t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0003c0003t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0004c0004t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0005c0007t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| a0006c0006t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0337 | EUR | GBR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0055 | EUR | GBR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | GBR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0327 | EUR | FIN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0217 | EUR | FIN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00438 | hp1 | a0004 | c0004 | t0002 | g0121 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00558 | hp2 | a0002 | c0002 | t0003 | g0064 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00597 | hp1 | a0002 | c0002 | t0003 | g0179 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00639 | hp1 | a0004 | c0004 | t0003 | g0215 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00642 | hp2 | a0004 | c0004 | t0003 | g0084 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00733 | hp1 | a0004 | c0004 | t0001 | g0213 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00741 | hp1 | a0003 | c0003 | t0001 | g0224 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0096 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01074 | hp2 | a0004 | c0004 | t0003 | g0073 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01099 | hp2 | a0002 | c0002 | t0003 | g0341 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01167 | hp2 | a0004 | c0004 | t0003 | g0083 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01175 | hp2 | a0004 | c0004 | t0003 | g0216 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0283 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0221 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0302 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01261 | hp2 | a0004 | c0004 | t0001 | g0059 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01496 | hp1 | a0003 | c0003 | t0001 | g0318 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0197 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | IBS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0271 | EUR | IBS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0053 | EUR | IBS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0289 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0192 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01891 | hp1 | a0003 | c0003 | t0003 | g0290 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0226 | AMR | PEL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0225 | AMR | PEL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02015 | hp1 | a0003 | c0003 | t0003 | g0258 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0178 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0287 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0317 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02071 | hp1 | a0001 | c0001 | t0012 | g0102 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02071 | hp2 | a0002 | c0002 | t0003 | g0259 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0201 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02132 | hp2 | a0002 | c0002 | t0003 | g0218 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02145 | hp1 | a0002 | c0002 | t0003 | g0314 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02145 | hp2 | a0003 | c0003 | t0005 | g0322 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PEL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0335 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02258 | hp1 | a0003 | c0003 | t0001 | g0331 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0237 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0286 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0301 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02451 | hp2 | a0002 | c0002 | t0003 | g0196 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02523 | hp1 | a0003 | c0003 | t0003 | g0205 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0336 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02572 | hp2 | a0001 | c0001 | t0010 | g0308 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0266 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02622 | hp1 | a0002 | c0008 | t0002 | g0049 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0189 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02630 | hp2 | a0002 | c0002 | t0006 | g0198 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02647 | hp1 | a0002 | c0002 | t0004 | g0001 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0338 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0253 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0329 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0288 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02717 | hp2 | a0002 | c0002 | t0004 | g0001 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02738 | hp1 | a0001 | c0005 | t0001 | g0276 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0033 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0295 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02818 | hp1 | a0005 | c0007 | t0003 | g0187 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0199 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0037 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02886 | hp2 | a0004 | c0004 | t0003 | g0304 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0232 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02896 | hp1 | a0003 | c0003 | t0003 | g0018 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0190 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02897 | hp2 | a0003 | c0003 | t0003 | g0017 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0200 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0204 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0236 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0278 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03041 | hp1 | a0004 | c0004 | t0002 | g0321 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0334 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03098 | hp1 | a0002 | c0002 | t0011 | g0305 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03098 | hp2 | a0002 | c0002 | t0004 | g0028 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0298 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0211 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0309 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0191 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03225 | hp1 | a0002 | c0002 | t0004 | g0027 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0333 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0039 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03486 | hp1 | a0002 | c0002 | t0006 | g0022 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03491 | hp1 | a0001 | c0001 | t0009 | g0241 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0306 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0297 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0315 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0300 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03579 | hp1 | a0003 | c0003 | t0005 | g0320 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0235 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0126 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0254 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0111 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0269 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG04115 | hp2 | a0002 | c0002 | t0003 | g0257 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0234 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG04228 | hp2 | a0001 | c0001 | t0008 | g0261 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18522 | hp1 | a0003 | c0003 | t0005 | g0281 | AFR | YRI | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18522 | hp2 | a0003 | c0003 | t0002 | g0319 | AFR | YRI | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18747 | hp1 | a0002 | c0002 | t0003 | g0214 | EAS | CHB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18747 | hp2 | a0003 | c0003 | t0001 | g0210 | EAS | CHB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0299 | AFR | YRI | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18906 | hp2 | a0003 | c0003 | t0005 | g0280 | AFR | YRI | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18940 | hp1 | a0004 | c0004 | t0002 | g0145 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18944 | hp2 | a0004 | c0004 | t0003 | g0115 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18945 | hp1 | a0003 | c0003 | t0003 | g0088 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18947 | hp1 | a0003 | c0003 | t0003 | g0139 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18953 | hp1 | a0003 | c0003 | t0003 | g0069 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18953 | hp2 | a0003 | c0003 | t0003 | g0208 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18954 | hp2 | a0003 | c0003 | t0003 | g0060 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18959 | hp2 | a0004 | c0004 | t0003 | g0219 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18960 | hp2 | a0003 | c0003 | t0003 | g0168 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18964 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18966 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18969 | hp1 | a0002 | c0002 | t0003 | g0123 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18969 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18970 | hp1 | a0001 | c0001 | t0007 | g0138 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18971 | hp1 | a0002 | c0002 | t0003 | g0184 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18973 | hp2 | a0004 | c0004 | t0003 | g0185 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18974 | hp1 | a0004 | c0004 | t0003 | g0116 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18979 | hp1 | a0003 | c0003 | t0003 | g0086 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18980 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18981 | hp1 | a0002 | c0002 | t0003 | g0057 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18985 | hp1 | a0003 | c0003 | t0003 | g0090 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0330 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18986 | hp2 | a0004 | c0004 | t0003 | g0120 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18990 | hp1 | a0003 | c0003 | t0003 | g0296 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18990 | hp2 | a0003 | c0003 | t0003 | g0181 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18993 | hp1 | a0004 | c0004 | t0003 | g0209 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18994 | hp2 | a0001 | c0001 | t0007 | g0161 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18995 | hp2 | a0002 | c0002 | t0003 | g0231 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18998 | hp2 | a0004 | c0004 | t0003 | g0105 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19000 | hp2 | a0002 | c0002 | t0003 | g0142 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19004 | hp2 | a0003 | c0003 | t0003 | g0220 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19005 | hp2 | a0003 | c0003 | t0002 | g0087 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19010 | hp1 | a0004 | c0004 | t0003 | g0134 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19012 | hp1 | a0004 | c0004 | t0003 | g0106 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0240 | AFR | LWK | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0264 | AFR | LWK | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0275 | AFR | LWK | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19043 | hp2 | a0002 | c0009 | t0001 | g0279 | AFR | LWK | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19081 | hp2 | a0003 | c0003 | t0002 | g0042 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19085 | hp1 | a0004 | c0004 | t0003 | g0172 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19088 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19091 | hp1 | a0003 | c0003 | t0003 | g0180 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19240 | hp1 | a0003 | c0003 | t0001 | g0030 | AFR | YRI | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0188 | AFR | YRI | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0332 | AFR | ASW | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ASW | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | GIH | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA20905 | hp2 | a0006 | c0006 | t0003 | g0068 | SAS | GIH | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02109 | hp2 | a0002 | c0002 | t0004 | g0029 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02486 | hp2 | a0004 | c0004 | t0003 | g0085 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0313 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0307 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG03471 | hp2 | a0003 | c0003 | t0002 | g0323 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG06807 | hp1 | a0002 | c0002 | t0004 | g0026 | AFR | USA | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| HG06807 | hp2 | a0003 | c0003 | t0001 | g0316 | AFR | USA | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0148 | AFR | USA | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0036 | AFR | USA | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA21309 | hp1 | a0003 | c0003 | t0003 | g0222 | AFR | LWK | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0212 | AFR | LWK | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0025 | REF | REF | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0268 | REF | REF | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29225139 | C | G | 4 | a0002 a0003 a0005 others(1): Show |
183 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(180): Show |
missense_variant | MODERATE | c.326C>G | p.Ala109Gly | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/15 | 469/2128 | 326/1332 | 109/443 | chr22 | 29225139 | |||
| chr22:29232285 | C | T | 1 | a0005 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.706C>T | p.Arg236Trp | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/15 | 849/2128 | 706/1332 | 236/443 | chr22 | 29232285 | |||
| chr22:29232304 | C | T | 1 | a0006 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.725C>T | p.Thr242Ile | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/15 | 868/2128 | 725/1332 | 242/443 | chr22 | 29232304 | |||
| chr22:29234348 | G | A | 3 | a0003 a0004 a0006 |
60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
missense_variant&splice_region_variant | MODERATE | c.1073G>A | p.Arg358Gln | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/15 | 1216/2128 | 1073/1332 | 358/443 | chr22 | 29234348 | |||
| chr22:29258907 | G | A | 1 | a0005 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1295G>A | p.Arg432Gln | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 1438/2128 | 1295/1332 | 432/443 | chr22 | 29258907 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29231121 | C | T | 1 | a0002c0009 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.567C>T | p.Pro189Pro | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/15 | 710/2128 | 567/1332 | 189/443 | chr22 | 29231121 | |||
| chr22:29231618 | C | T | 1 | a0002c0008 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.612C>T | p.Pro204Pro | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 7/15 | 755/2128 | 612/1332 | 204/443 | chr22 | 29231618 | |||
| chr22:29232275 | G | A | 1 | a0001c0005 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.696G>A | p.Gly232Gly | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/15 | 839/2128 | 696/1332 | 232/443 | chr22 | 29232275 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29205912 | C | T | 2 | a0001c0001t0007 a0001c0001t0012 |
3 | HG02071.hp1 NA18970.hp1 NA18994.hp2 |
5_prime_UTR_variant | MODIFIER | c.-127C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/15 | 127 | chr22 | 29205912 | ||||||
| chr22:29205916 | C | T | 1 | a0002c0002t0011 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-123C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/15 | 123 | chr22 | 29205916 | ||||||
| chr22:29206020 | G | A | 1 | a0002c0002t0004 | 6 | HG02109.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-19G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/15 | 19 | chr22 | 29206020 | ||||||
| chr22:29258957 | C | T | 1 | a0002c0002t0006 | 2 | HG02630.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*13C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 13 | chr22 | 29258957 | ||||||
| chr22:29259272 | G | C | 1 | a0001c0001t0008 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*328G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 328 | chr22 | 29259272 | ||||||
| chr22:29259320 | C | G | 1 | a0001c0001t0010 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*376C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 376 | chr22 | 29259320 | ||||||
| chr22:29259382 | C | T | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(17): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*438C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 438 | chr22 | 29259382 | ||||||
| chr22:29259427 | C | T | 13 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(10): Show |
121 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*483C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 483 | chr22 | 29259427 | ||||||
| chr22:29259506 | G | A | 2 | a0002c0002t0011 a0003c0003t0005 |
5 | HG02145.hp2 HG03098.hp1 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*562G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 562 | chr22 | 29259506 | ||||||
| chr22:29259550 | G | A | 1 | a0001c0001t0009 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*606G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 606 | chr22 | 29259550 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29206147 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0339 a0001c0001t0001g0340 others(3): Show |
7 | HG00099.hp1 HG01099.hp2 HG02148.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.101+8C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206147 | |||||||
| chr22:29206170 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(2): Show |
5 | HG01081.hp2 HG01109.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+31T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206170 | |||||||
| chr22:29206250 | T | TGAG | 12 | a0001c0001t0002g0013 a0001c0001t0002g0023 a0001c0001t0002g0024 others(9): Show |
12 | HG01081.hp1 HG01255.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.101+113_101+115dup others(3): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 29206250 | ||||||
| chr22:29206500 | C | T | 6 | a0001c0001t0003g0334 a0001c0001t0003g0335 a0001c0001t0003g0336 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+361C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206500 | |||||||
| chr22:29206503 | C | G | 7 | a0001c0001t0001g0325 a0001c0001t0001g0328 a0001c0001t0003g0326 others(4): Show |
7 | HG00280.hp1 HG02698.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+364C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206503 | |||||||
| chr22:29206663 | A | G | 11 | a0002c0002t0001g0313 a0002c0002t0002g0315 a0002c0002t0003g0314 others(8): Show |
11 | HG01496.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+524A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206663 | |||||||
| chr22:29206700 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.101+561C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206700 | |||||||
| chr22:29206801 | C | T | 1 | a0002c0002t0001g0311 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.101+662C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206801 | |||||||
| chr22:29206930 | T | C | 6 | a0002c0002t0004g0001 a0002c0002t0004g0026 a0002c0002t0004g0027 others(3): Show |
7 | HG02109.hp2 HG02258.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+791T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206930 | |||||||
| chr22:29206933 | T | C | 11 | a0001c0001t0001g0031 a0001c0001t0003g0035 a0002c0002t0001g0032 others(8): Show |
11 | HG02486.hp1 HG02723.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+794T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206933 | |||||||
| chr22:29206982 | G | A | 157 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0043 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.101+843G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206982 | |||||||
| chr22:29207007 | G | A | 1 | a0004c0004t0003g0185 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.101+868G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207007 | |||||||
| chr22:29207079 | G | A | 1 | a0002c0002t0002g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.101+940G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207079 | |||||||
| chr22:29207092 | C | A | 3 | a0002c0002t0001g0313 a0002c0002t0002g0315 a0002c0002t0003g0314 |
3 | HG02145.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.101+953C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207092 | |||||||
| chr22:29207266 | G | A | 6 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0001g0190 others(3): Show |
6 | HG01884.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+1127G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207266 | |||||||
| chr22:29207320 | G | T | 1 | a0001c0001t0001g0310 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101+1181G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207320 | |||||||
| chr22:29207494 | CTCAGAAA | C | 5 | a0002c0002t0004g0001 a0002c0002t0004g0026 a0002c0002t0004g0027 others(2): Show |
6 | HG02109.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+1358_101+1364d others(9): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 29207494 | ||||||
| chr22:29207552 | G | A | 22 | a0002c0002t0002g0193 a0002c0002t0002g0194 a0002c0002t0002g0195 others(19): Show |
22 | HG00408.hp1 HG00558.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.101+1413G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207552 | |||||||
| chr22:29207622 | A | G | 217 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(214): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.101+1483A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207622 | |||||||
| chr22:29207636 | A | G | 1 | a0003c0003t0001g0210 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.101+1497A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207636 | |||||||
| chr22:29207644 | G | T | 3 | a0001c0001t0002g0307 a0001c0001t0003g0309 a0001c0001t0010g0308 |
3 | HG02572.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.101+1505G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207644 | |||||||
| chr22:29207757 | C | T | 21 | a0001c0001t0001g0277 a0001c0001t0002g0278 a0001c0005t0001g0276 others(18): Show |
21 | HG00408.hp1 HG00558.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.101+1618C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207757 | |||||||
| chr22:29207807 | G | A | 298 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.101+1668G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207807 | |||||||
| chr22:29207875 | G | A | 7 | a0002c0002t0001g0313 a0002c0002t0002g0315 a0002c0002t0003g0314 others(4): Show |
7 | HG02145.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+1736G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207875 | |||||||
| chr22:29207918 | G | C | 10 | a0001c0001t0002g0013 a0002c0002t0001g0016 a0002c0002t0001g0020 others(7): Show |
10 | HG01081.hp1 HG01255.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+1779G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207918 | |||||||
| chr22:29208141 | A | G | 56 | a0001c0001t0001g0223 a0001c0001t0002g0006 a0001c0001t0002g0013 others(53): Show |
57 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.101+2002A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208141 | |||||||
| chr22:29208158 | C | G | 6 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0001g0190 others(3): Show |
6 | HG01884.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+2019C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208158 | |||||||
| chr22:29208286 | G | C | 179 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(176): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.101+2147G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208286 | |||||||
| chr22:29208321 | C | T | 24 | a0001c0001t0001g0223 a0001c0001t0002g0006 a0001c0001t0002g0228 others(21): Show |
24 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.101+2182C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208321 | |||||||
| chr22:29208375 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.101+2236C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208375 | |||||||
| chr22:29208572 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(182): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.101+2433G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208572 | |||||||
| chr22:29208798 | T | C | 241 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(238): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.101+2659T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208798 | |||||||
| chr22:29208902 | C | T | 1 | a0002c0002t0002g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.101+2763C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208902 | |||||||
| chr22:29208983 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.101+2844C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208983 | |||||||
| chr22:29209055 | C | T | 1 | a0004c0004t0003g0209 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.101+2916C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209055 | |||||||
| chr22:29209115 | G | A | 1 | a0001c0001t0002g0013 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.101+2976G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209115 | |||||||
| chr22:29209129 | T | C | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0002c0002t0001g0211 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.101+2990T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209129 | |||||||
| chr22:29209146 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.101+3007A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209146 | |||||||
| chr22:29209234 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.101+3095G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209234 | |||||||
| chr22:29209582 | G | A | 24 | a0001c0001t0001g0223 a0001c0001t0002g0006 a0001c0001t0002g0228 others(21): Show |
24 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.101+3443G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209582 | |||||||
| chr22:29209633 | A | G | 1 | a0002c0002t0002g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.101+3494A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209633 | |||||||
| chr22:29209689 | C | T | 1 | a0002c0002t0002g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.101+3550C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209689 | |||||||
| chr22:29209735 | A | G | 14 | a0001c0001t0002g0013 a0002c0002t0001g0016 a0002c0002t0001g0020 others(11): Show |
14 | HG01081.hp1 HG01255.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.101+3596A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209735 | |||||||
| chr22:29209818 | A | G | 4 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0002g0037 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+3679A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209818 | |||||||
| chr22:29209962 | G | A | 1 | a0003c0003t0002g0042 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.101+3823G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209962 | |||||||
| chr22:29210168 | C | G | 4 | a0003c0003t0001g0316 a0003c0003t0001g0317 a0003c0003t0001g0318 others(1): Show |
4 | HG01496.hp1 HG02055.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.101+4029C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210168 | |||||||
| chr22:29210168 | C | T | 10 | a0001c0001t0002g0013 a0002c0002t0001g0016 a0002c0002t0001g0020 others(7): Show |
10 | HG01081.hp1 HG01255.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+4029C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210168 | |||||||
| chr22:29210250 | AT | A | 219 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(216): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.101+4131delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 29210250 | ||||||
| chr22:29210254 | T | C | 8 | a0002c0002t0001g0016 a0002c0002t0001g0020 a0002c0002t0001g0021 others(5): Show |
8 | HG01081.hp1 HG01255.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.101+4115T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210254 | |||||||
| chr22:29210456 | G | A | 1 | a0004c0004t0001g0213 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.101+4317G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210456 | |||||||
| chr22:29210483 | G | C | 1 | a0002c0009t0001g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.101+4344G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210483 | |||||||
| chr22:29210593 | C | T | 12 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(9): Show |
12 | HG01074.hp1 HG01993.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.102-4333C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210593 | |||||||
| chr22:29210877 | G | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0043 others(147): Show |
152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.102-4049G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210877 | |||||||
| chr22:29210918 | C | T | 19 | a0001c0001t0001g0223 a0001c0001t0002g0006 a0001c0001t0003g0217 others(16): Show |
19 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.102-4008C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210918 | |||||||
| chr22:29210957 | A | AGT | 18 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0001c0001t0002g0146 others(15): Show |
18 | HG00639.hp2 HG01109.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.102-3956_102-3955d others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 29210957 | ||||||
| chr22:29211346 | C | T | 5 | a0002c0002t0004g0001 a0002c0002t0004g0026 a0002c0002t0004g0027 others(2): Show |
6 | HG02109.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-3580C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211346 | |||||||
| chr22:29211381 | G | C | 1 | a0002c0002t0001g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.102-3545G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211381 | |||||||
| chr22:29211418 | C | T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(192): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.102-3508C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211418 | |||||||
| chr22:29211467 | C | T | 3 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0002c0002t0001g0234 |
3 | HG02738.hp2 HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.102-3459C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211467 | |||||||
| chr22:29211480 | T | A | 12 | a0001c0001t0003g0334 a0001c0001t0003g0335 a0001c0001t0003g0336 others(9): Show |
12 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.102-3446T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211480 | |||||||
| chr22:29211550 | T | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0164 |
2 | HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.102-3376T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211550 | |||||||
| chr22:29211576 | A | G | 1 | a0004c0004t0002g0145 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.102-3350A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211576 | |||||||
| chr22:29211727 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102-3199A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211727 | |||||||
| chr22:29211938 | TA | T | 24 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(21): Show |
24 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.102-2987delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211938 | |||||||
| chr22:29212267 | G | A | 17 | a0001c0001t0003g0334 a0001c0001t0003g0335 a0001c0001t0003g0336 others(14): Show |
18 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.102-2659G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212267 | |||||||
| chr22:29212287 | C | T | 241 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(238): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.102-2639C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212287 | |||||||
| chr22:29212307 | A | T | 1 | a0001c0001t0001g0012 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.102-2619A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212307 | |||||||
| chr22:29212335 | G | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(237): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.102-2591G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212335 | |||||||
| chr22:29212409 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.102-2517C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212409 | |||||||
| chr22:29212569 | C | CT | 16 | a0001c0001t0001g0007 a0001c0001t0001g0141 a0001c0001t0001g0163 others(13): Show |
17 | HG00099.hp1 HG00733.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.102-2345dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 29212569 | ||||||
| chr22:29212626 | C | T | 19 | a0001c0001t0001g0223 a0001c0001t0002g0006 a0001c0001t0003g0217 others(16): Show |
19 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.102-2300C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212626 | |||||||
| chr22:29212627 | G | A | 1 | a0002c0002t0002g0044 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.102-2299G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212627 | |||||||
| chr22:29212757 | G | C | 2 | a0002c0002t0002g0288 a0002c0002t0002g0289 |
2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.102-2169G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212757 | |||||||
| chr22:29212779 | G | C | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0002c0002t0001g0211 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.102-2147G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212779 | |||||||
| chr22:29212939 | C | T | 1 | a0002c0002t0002g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.102-1987C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212939 | |||||||
| chr22:29212940 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 |
3 | HG01256.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.102-1986G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212940 | |||||||
| chr22:29213396 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.102-1530A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29213396 | |||||||
| chr22:29213488 | A | G | 2 | a0002c0002t0002g0286 a0002c0002t0002g0287 |
2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.102-1438A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29213488 | |||||||
| chr22:29213586 | G | A | 1 | a0002c0009t0001g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.102-1340G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29213586 | |||||||
| chr22:29213598 | G | A | 1 | a0002c0002t0001g0235 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.102-1328G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29213598 | |||||||
| chr22:29214037 | C | T | 7 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0001g0190 others(4): Show |
7 | HG01884.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-889C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214037 | |||||||
| chr22:29214149 | A | G | 241 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(238): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.102-777A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214149 | |||||||
| chr22:29214150 | C | T | 5 | a0002c0002t0004g0001 a0002c0002t0004g0026 a0002c0002t0004g0027 others(2): Show |
6 | HG02109.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-776C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214150 | |||||||
| chr22:29214179 | G | A | 5 | a0001c0001t0003g0047 a0002c0002t0002g0045 a0002c0002t0002g0046 others(2): Show |
5 | NA18944.hp1 NA18966.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-747G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214179 | |||||||
| chr22:29214248 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.102-678T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214248 | |||||||
| chr22:29214333 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.102-593A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214333 | |||||||
| chr22:29214343 | T | C | 335 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(332): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.102-583T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214343 | |||||||
| chr22:29214411 | A | G | 12 | a0001c0001t0003g0334 a0001c0001t0003g0335 a0001c0001t0003g0336 others(9): Show |
12 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.102-515A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214411 | |||||||
| chr22:29214654 | C | T | 1 | a0001c0001t0007g0138 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.102-272C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214654 | |||||||
| chr22:29215247 | T | C | 3 | a0002c0002t0001g0313 a0002c0002t0002g0315 a0002c0002t0003g0314 |
3 | HG02145.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.215+208T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 2/14 | chr22 | 29215247 | |||||||
| chr22:29215360 | G | T | 2 | a0002c0002t0002g0288 a0002c0002t0002g0289 |
2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.216-167G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 2/14 | chr22 | 29215360 | |||||||
| chr22:29215876 | A | G | 2 | a0002c0002t0001g0211 a0002c0002t0001g0212 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.319+246A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29215876 | |||||||
| chr22:29215917 | G | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(14): Show |
17 | HG00741.hp1 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.319+287G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29215917 | |||||||
| chr22:29215979 | C | T | 16 | a0001c0001t0001g0291 a0001c0001t0002g0023 a0001c0001t0002g0024 others(13): Show |
16 | HG01070.hp2 HG01081.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.319+349C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29215979 | |||||||
| chr22:29216051 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.319+421C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216051 | |||||||
| chr22:29216321 | A | G | 1 | a0001c0001t0001g0003 | 2 | HG00544.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.319+691A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216321 | |||||||
| chr22:29216331 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.319+701C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216331 | |||||||
| chr22:29216473 | G | C | 14 | a0002c0002t0001g0313 a0002c0002t0002g0014 a0002c0002t0002g0315 others(11): Show |
14 | HG01346.hp1 HG01496.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.319+843G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216473 | |||||||
| chr22:29216484 | G | A | 6 | a0003c0003t0002g0323 a0003c0003t0005g0280 a0003c0003t0005g0281 others(3): Show |
6 | HG02145.hp2 HG03041.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.319+854G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216484 | |||||||
| chr22:29216492 | G | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(152): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.319+862G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216492 | |||||||
| chr22:29216514 | A | C | 1 | a0002c0002t0002g0288 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.319+884A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216514 | |||||||
| chr22:29216519 | A | G | 50 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(47): Show |
51 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.319+889A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216519 | |||||||
| chr22:29216579 | G | A | 2 | a0002c0002t0001g0236 a0002c0002t0001g0237 |
2 | HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.319+949G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216579 | |||||||
| chr22:29216714 | C | T | 1 | a0002c0002t0006g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.319+1084C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216714 | |||||||
| chr22:29216747 | G | A | 337 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(334): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.319+1117G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216747 | |||||||
| chr22:29216912 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.319+1282G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216912 | |||||||
| chr22:29216945 | G | A | 25 | a0001c0001t0001g0282 a0001c0001t0002g0006 a0001c0001t0003g0217 others(22): Show |
26 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.319+1315G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216945 | |||||||
| chr22:29216959 | C | G | 3 | a0001c0001t0001g0292 a0001c0001t0002g0293 a0002c0009t0001g0279 |
3 | HG02622.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.319+1329C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216959 | |||||||
| chr22:29217012 | G | A | 7 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0001g0190 others(4): Show |
7 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+1382G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217012 | |||||||
| chr22:29217108 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.319+1478G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217108 | |||||||
| chr22:29217379 | G | A | 16 | a0001c0001t0003g0334 a0001c0001t0003g0335 a0001c0001t0003g0336 others(13): Show |
16 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.319+1749G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217379 | |||||||
| chr22:29217386 | T | A | 4 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0002g0037 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.319+1756T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217386 | |||||||
| chr22:29217450 | C | T | 36 | a0001c0001t0001g0043 a0001c0001t0001g0162 a0001c0001t0001g0223 others(33): Show |
36 | HG00423.hp2 HG01515.hp2 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.319+1820C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217450 | |||||||
| chr22:29217452 | G | T | 66 | a0001c0001t0001g0043 a0001c0001t0001g0162 a0001c0001t0001g0223 others(63): Show |
67 | HG00423.hp2 HG01346.hp1 HG01496.hp1 others(64): Show |
intron_variant | MODIFIER | c.319+1822G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217452 | |||||||
| chr22:29217462 | G | A | 9 | a0001c0001t0003g0334 a0001c0001t0003g0335 a0001c0001t0003g0336 others(6): Show |
9 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.319+1832G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217462 | |||||||
| chr22:29217606 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.319+1976G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217606 | |||||||
| chr22:29217878 | C | G | 1 | a0002c0002t0001g0118 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.319+2248C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217878 | |||||||
| chr22:29217941 | A | G | 64 | a0001c0001t0001g0007 a0001c0001t0001g0176 a0001c0001t0001g0263 others(61): Show |
67 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.319+2311A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217941 | |||||||
| chr22:29217965 | T | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(6): Show |
9 | HG01081.hp2 HG01109.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.319+2335T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217965 | |||||||
| chr22:29218001 | G | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(12): Show |
15 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.319+2371G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218001 | |||||||
| chr22:29218054 | TCTC | T | 10 | a0002c0002t0001g0313 a0002c0002t0002g0014 a0002c0002t0002g0315 others(7): Show |
10 | HG01346.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.319+2428_319+2430d others(5): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29218054 | ||||||
| chr22:29218111 | C | T | 1 | a0001c0001t0002g0284 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.319+2481C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218111 | |||||||
| chr22:29218195 | G | A | 1 | a0002c0002t0002g0240 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.319+2565G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218195 | |||||||
| chr22:29218205 | G | A | 1 | a0002c0008t0002g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.319+2575G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218205 | |||||||
| chr22:29218314 | C | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0339 a0001c0001t0001g0340 others(12): Show |
16 | HG00099.hp1 HG01099.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.319+2684C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218314 | |||||||
| chr22:29218362 | C | G | 10 | a0001c0001t0001g0031 a0001c0001t0002g0265 a0001c0001t0002g0285 others(7): Show |
10 | HG01496.hp2 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.319+2732C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218362 | |||||||
| chr22:29218577 | A | G | 7 | a0001c0001t0003g0035 a0002c0002t0001g0038 a0002c0002t0001g0039 others(4): Show |
7 | HG02486.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+2947A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218577 | |||||||
| chr22:29218601 | A | G | 1 | a0002c0002t0002g0269 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.319+2971A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218601 | |||||||
| chr22:29218688 | C | T | 2 | a0001c0001t0002g0297 a0001c0001t0002g0306 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.319+3058C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218688 | |||||||
| chr22:29218689 | G | A | 143 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(140): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.319+3059G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218689 | |||||||
| chr22:29218775 | T | A | 2 | a0001c0001t0001g0325 a0002c0002t0001g0324 |
2 | NA18942.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.319+3145T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218775 | |||||||
| chr22:29218940 | T | C | 32 | a0001c0001t0001g0176 a0001c0001t0001g0263 a0001c0001t0001g0277 others(29): Show |
33 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.319+3310T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218940 | |||||||
| chr22:29219059 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.319+3429A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219059 | |||||||
| chr22:29219268 | C | G | 1 | a0002c0002t0002g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.319+3638C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219268 | |||||||
| chr22:29219306 | G | A | 6 | a0002c0002t0004g0001 a0002c0002t0004g0026 a0002c0002t0004g0027 others(3): Show |
7 | HG02109.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.319+3676G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219306 | |||||||
| chr22:29219375 | C | T | 14 | a0002c0002t0001g0313 a0002c0002t0002g0014 a0002c0002t0002g0315 others(11): Show |
14 | HG01346.hp1 HG01496.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.319+3745C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219375 | |||||||
| chr22:29219377 | C | T | 1 | a0002c0002t0004g0029 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.319+3747C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219377 | |||||||
| chr22:29219547 | A | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0339 a0001c0001t0001g0340 others(3): Show |
7 | HG00099.hp1 HG01099.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+3917A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219547 | |||||||
| chr22:29219613 | C | CA | 10 | a0001c0001t0001g0050 a0001c0001t0003g0035 a0002c0002t0001g0038 others(7): Show |
10 | HG00639.hp1 HG01175.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.319+3993dupA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29219613 | ||||||
| chr22:29219743 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(174): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.319+4113C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219743 | |||||||
| chr22:29219801 | T | G | 4 | a0003c0003t0001g0030 a0003c0003t0001g0316 a0003c0003t0001g0317 others(1): Show |
4 | HG01496.hp1 HG02055.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+4171T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219801 | |||||||
| chr22:29219824 | C | G | 3 | a0002c0002t0001g0313 a0002c0002t0002g0315 a0002c0002t0003g0314 |
3 | HG02145.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.319+4194C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219824 | |||||||
| chr22:29220025 | A | G | 29 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(26): Show |
30 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.319+4395A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220025 | |||||||
| chr22:29220037 | C | G | 7 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0001g0190 others(4): Show |
7 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+4407C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220037 | |||||||
| chr22:29220188 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.319+4558G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220188 | |||||||
| chr22:29220276 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(180): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.319+4646A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220276 | |||||||
| chr22:29220287 | C | T | 8 | a0001c0001t0001g0135 a0001c0001t0003g0002 a0001c0001t0003g0130 others(5): Show |
9 | HG01346.hp1 NA18955.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.319+4657C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220287 | |||||||
| chr22:29220744 | A | C | 3 | a0002c0002t0001g0313 a0002c0002t0002g0315 a0002c0002t0003g0314 |
3 | HG02145.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.320-4389A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220744 | |||||||
| chr22:29220759 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.320-4374C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220759 | |||||||
| chr22:29220957 | G | A | 6 | a0002c0002t0001g0299 a0002c0002t0001g0300 a0002c0002t0001g0303 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.320-4176G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220957 | |||||||
| chr22:29220994 | T | G | 8 | a0002c0002t0002g0033 a0002c0002t0002g0240 a0002c0002t0004g0001 others(5): Show |
9 | HG02109.hp2 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.320-4139T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220994 | |||||||
| chr22:29221053 | C | G | 1 | a0002c0002t0002g0192 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.320-4080C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29221053 | |||||||
| chr22:29221066 | C | CGT | 8 | a0001c0001t0002g0114 a0001c0001t0003g0309 a0001c0001t0003g0336 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.320-4010_320-4009d others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221066 | C | CGTGT | 9 | a0001c0001t0001g0310 a0002c0002t0001g0298 a0002c0002t0002g0269 others(6): Show |
9 | HG02145.hp2 HG02258.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.320-4012_320-4009d others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221066 | CGT | C | 20 | a0001c0001t0001g0267 a0001c0001t0002g0104 a0001c0001t0002g0108 others(17): Show |
21 | HG00609.hp2 HG01243.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.320-4010_320-4009d others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221066 | CGTGT | C | 29 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0100 others(26): Show |
29 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.320-4012_320-4009d others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221066 | CGTGTGT | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(46): Show |
50 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.320-4014_320-4009d others(8): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221066 | CGTGTGTG others(1): Show |
C | 25 | a0001c0001t0001g0066 a0001c0001t0001g0070 a0001c0001t0001g0141 others(22): Show |
25 | HG00558.hp2 HG00597.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.320-4016_320-4009d others(10): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221066 | CGTGTGTG others(3): Show |
C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(27): Show |
30 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.320-4018_320-4009d others(12): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221066 | CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0002g0053 a0003c0003t0003g0290 |
2 | HG01517.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.320-4020_320-4009d others(14): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221066 | CGTGTGTG others(9): Show |
C | 11 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0188 others(8): Show |
11 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.320-4024_320-4009d others(18): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221066 | CGTGTGTG others(11): Show |
C | 34 | a0001c0001t0001g0162 a0001c0001t0001g0176 a0001c0001t0001g0260 others(31): Show |
35 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.320-4026_320-4009d others(20): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221066 | CGTGTGTG others(13): Show |
C | 54 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0043 others(51): Show |
56 | HG00423.hp2 HG01070.hp2 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.320-4028_320-4009d others(22): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221066 | CGTGTGTG others(15): Show |
C | 42 | a0001c0001t0001g0263 a0001c0001t0001g0277 a0001c0001t0001g0282 others(39): Show |
43 | HG00558.hp1 HG00733.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.320-4030_320-4009d others(24): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221066 | CGTGTGTG others(17): Show |
C | 12 | a0001c0001t0002g0006 a0001c0001t0003g0217 a0001c0001t0003g0239 others(9): Show |
12 | HG00280.hp2 HG00639.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.320-4032_320-4009d others(26): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221066 | CGTGTGTG others(19): Show |
C | 1 | a0001c0001t0003g0337 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.320-4034_320-4009d others(28): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221066 | CGTGTGTG others(21): Show |
C | 1 | a0003c0003t0001g0224 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.320-4036_320-4009d others(30): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | ||||||
| chr22:29221132 | G | T | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.320-4001G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29221132 | |||||||
| chr22:29221249 | GGGA | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(135): Show |
139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.320-3879_320-3877d others(5): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221249 | ||||||
| chr22:29221331 | A | G | 89 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0176 others(86): Show |
92 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.320-3802A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29221331 | |||||||
| chr22:29221500 | G | A | 1 | a0002c0002t0002g0174 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.320-3633G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29221500 | |||||||
| chr22:29221756 | G | A | 1 | a0003c0003t0003g0168 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.320-3377G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29221756 | |||||||
| chr22:29221963 | A | T | 1 | a0003c0003t0003g0290 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.320-3170A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29221963 | |||||||
| chr22:29222011 | G | A | 337 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(334): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.320-3122G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222011 | |||||||
| chr22:29222043 | A | G | 6 | a0001c0001t0001g0325 a0001c0001t0001g0328 a0001c0001t0003g0326 others(3): Show |
6 | HG00280.hp1 HG02698.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-3090A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222043 | |||||||
| chr22:29222118 | T | A | 7 | a0001c0001t0003g0035 a0002c0002t0001g0038 a0002c0002t0001g0039 others(4): Show |
7 | HG02486.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.320-3015T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222118 | |||||||
| chr22:29222204 | C | T | 2 | a0002c0002t0001g0211 a0002c0002t0001g0212 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.320-2929C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222204 | |||||||
| chr22:29222237 | G | A | 7 | a0002c0002t0002g0033 a0002c0002t0002g0240 a0002c0002t0004g0001 others(4): Show |
8 | HG02109.hp2 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.320-2896G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222237 | |||||||
| chr22:29222329 | A | G | 1 | a0002c0002t0002g0288 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.320-2804A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222329 | |||||||
| chr22:29222386 | G | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0339 a0001c0001t0001g0340 others(3): Show |
7 | HG00099.hp1 HG01099.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.320-2747G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222386 | |||||||
| chr22:29222406 | CT | C | 282 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(279): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.320-2708delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29222406 | ||||||
| chr22:29222406 | CTT | C | 42 | a0001c0001t0001g0282 a0001c0001t0002g0006 a0001c0001t0002g0244 others(39): Show |
43 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.320-2709_320-2708d others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29222406 | ||||||
| chr22:29222524 | C | G | 32 | a0001c0001t0001g0176 a0001c0001t0001g0263 a0001c0001t0001g0277 others(29): Show |
33 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.320-2609C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222524 | |||||||
| chr22:29222595 | G | A | 2 | a0002c0002t0001g0211 a0002c0002t0001g0212 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.320-2538G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222595 | |||||||
| chr22:29222610 | G | T | 1 | a0003c0003t0003g0090 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.320-2523G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222610 | |||||||
| chr22:29222656 | G | A | 3 | a0002c0002t0001g0110 a0003c0003t0002g0042 a0003c0003t0003g0060 |
3 | NA18954.hp2 NA19081.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.320-2477G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222656 | |||||||
| chr22:29222916 | C | G | 1 | a0002c0002t0002g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.320-2217C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222916 | |||||||
| chr22:29223009 | T | C | 22 | a0001c0001t0001g0031 a0001c0001t0001g0291 a0001c0001t0002g0023 others(19): Show |
22 | HG01070.hp2 HG01081.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.320-2124T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223009 | |||||||
| chr22:29223016 | A | G | 2 | a0001c0001t0001g0058 a0004c0004t0001g0059 |
2 | HG01261.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.320-2117A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223016 | |||||||
| chr22:29223022 | C | T | 2 | a0001c0001t0001g0292 a0001c0001t0002g0293 |
2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.320-2111C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223022 | |||||||
| chr22:29223028 | T | C | 12 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0001g0190 others(9): Show |
12 | HG01884.hp2 HG02145.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.320-2105T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223028 | |||||||
| chr22:29223047 | C | T | 26 | a0001c0001t0001g0263 a0001c0001t0001g0282 a0001c0001t0002g0006 others(23): Show |
27 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.320-2086C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223047 | |||||||
| chr22:29223476 | G | C | 2 | a0001c0001t0002g0297 a0001c0001t0002g0306 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.320-1657G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223476 | |||||||
| chr22:29223600 | T | C | 1 | a0002c0002t0001g0236 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.320-1533T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223600 | |||||||
| chr22:29223604 | A | C | 26 | a0001c0001t0001g0263 a0001c0001t0001g0282 a0001c0001t0002g0006 others(23): Show |
27 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.320-1529A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223604 | |||||||
| chr22:29223745 | A | AG | 7 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0002g0037 others(4): Show |
7 | HG02258.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.320-1387dupG | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29223745 | ||||||
| chr22:29223778 | C | A | 1 | a0002c0002t0002g0201 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.320-1355C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223778 | |||||||
| chr22:29224079 | C | T | 2 | a0001c0001t0002g0108 a0001c0001t0003g0109 |
2 | NA18939.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.320-1054C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224079 | |||||||
| chr22:29224135 | G | C | 1 | a0002c0002t0003g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.320-998G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224135 | |||||||
| chr22:29224186 | C | T | 1 | a0001c0001t0002g0278 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.320-947C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224186 | |||||||
| chr22:29224187 | G | A | 30 | a0001c0001t0001g0043 a0001c0001t0001g0162 a0001c0001t0001g0223 others(27): Show |
30 | HG00423.hp2 HG01515.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.320-946G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224187 | |||||||
| chr22:29224243 | C | T | 153 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(150): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.320-890C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224243 | |||||||
| chr22:29224316 | C | T | 3 | a0002c0002t0002g0221 a0003c0003t0003g0222 a0004c0004t0001g0213 |
3 | HG00733.hp1 HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.320-817C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224316 | |||||||
| chr22:29224336 | A | C | 79 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0052 others(76): Show |
81 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.320-797A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224336 | |||||||
| chr22:29224396 | C | T | 2 | a0002c0002t0001g0137 a0002c0002t0001g0143 |
2 | NA18943.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.320-737C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224396 | |||||||
| chr22:29224469 | G | C | 6 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0001g0190 others(3): Show |
6 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-664G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224469 | |||||||
| chr22:29224472 | T | C | 29 | a0001c0001t0001g0135 a0001c0001t0001g0291 a0001c0001t0001g0294 others(26): Show |
30 | HG01070.hp2 HG01081.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.320-661T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224472 | |||||||
| chr22:29224499 | G | T | 1 | a0002c0002t0002g0240 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320-634G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224499 | |||||||
| chr22:29224573 | T | A | 38 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(35): Show |
40 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.320-560T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224573 | |||||||
| chr22:29224575 | A | G | 330 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(327): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.320-558A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224575 | |||||||
| chr22:29224625 | C | T | 1 | a0001c0001t0007g0161 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.320-508C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224625 | |||||||
| chr22:29224690 | G | C | 1 | a0002c0002t0002g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.320-443G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224690 | |||||||
| chr22:29224911 | C | T | 7 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.320-222C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224911 | |||||||
| chr22:29224913 | C | T | 1 | a0002c0002t0002g0107 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.320-220C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224913 | |||||||
| chr22:29225072 | CA | C | 21 | a0002c0002t0001g0016 a0002c0002t0001g0232 a0002c0002t0001g0236 others(18): Show |
21 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.320-60delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29225072 | |||||||
| chr22:29225079 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.320-54G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29225079 | |||||||
| chr22:29225414 | C | T | 1 | a0002c0002t0002g0159 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.403+198C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29225414 | |||||||
| chr22:29225488 | C | T | 334 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(331): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.403+272C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29225488 | |||||||
| chr22:29225594 | G | T | 1 | a0001c0001t0008g0261 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.403+378G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29225594 | |||||||
| chr22:29225656 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.403+440G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29225656 | |||||||
| chr22:29225872 | T | C | 335 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(332): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.404-618T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29225872 | |||||||
| chr22:29225911 | G | A | 1 | a0001c0001t0002g0108 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.404-579G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29225911 | |||||||
| chr22:29225999 | C | T | 1 | a0002c0002t0004g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.404-491C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29225999 | |||||||
| chr22:29226000 | G | A | 24 | a0001c0001t0001g0072 a0001c0001t0001g0176 a0001c0001t0001g0312 others(21): Show |
24 | HG01346.hp1 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.404-490G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226000 | |||||||
| chr22:29226019 | C | A | 1 | a0002c0002t0001g0298 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.404-471C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226019 | |||||||
| chr22:29226139 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.404-351G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226139 | |||||||
| chr22:29226175 | C | T | 2 | a0002c0002t0002g0191 a0002c0002t0002g0275 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.404-315C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226175 | |||||||
| chr22:29226178 | C | A | 1 | a0004c0004t0003g0073 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.404-312C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226178 | |||||||
| chr22:29226178 | C | T | 4 | a0003c0003t0001g0030 a0003c0003t0001g0316 a0003c0003t0001g0317 others(1): Show |
4 | HG01496.hp1 HG02055.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-312C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226178 | |||||||
| chr22:29226265 | G | C | 15 | a0001c0001t0001g0031 a0001c0001t0001g0292 a0001c0001t0002g0023 others(12): Show |
15 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.404-225G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226265 | |||||||
| chr22:29226322 | C | T | 3 | a0002c0002t0002g0193 a0002c0002t0002g0194 a0002c0002t0002g0195 |
3 | NA18955.hp2 NA19005.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.404-168C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226322 | |||||||
| chr22:29226387 | A | G | 16 | a0001c0001t0001g0282 a0002c0002t0001g0188 a0002c0002t0001g0189 others(13): Show |
17 | HG01496.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-103A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226387 | |||||||
| chr22:29226415 | C | T | 1 | a0002c0002t0002g0182 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.404-75C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226415 | |||||||
| chr22:29226647 | A | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01081.hp2 HG01109.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.465+96A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29226647 | |||||||
| chr22:29226674 | G | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | NA18947.hp2 NA19011.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.465+123G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29226674 | |||||||
| chr22:29226716 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0091 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.465+165C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29226716 | |||||||
| chr22:29226833 | G | T | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.465+282G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29226833 | |||||||
| chr22:29226941 | C | T | 15 | a0001c0001t0001g0031 a0001c0001t0001g0292 a0001c0001t0002g0023 others(12): Show |
15 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.465+390C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29226941 | |||||||
| chr22:29226988 | T | A | 181 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(178): Show |
183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.465+437T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29226988 | |||||||
| chr22:29227000 | C | A | 14 | a0001c0001t0001g0282 a0002c0002t0001g0188 a0002c0002t0001g0189 others(11): Show |
15 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.465+449C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227000 | |||||||
| chr22:29227045 | A | T | 1 | a0002c0002t0002g0256 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.465+494A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227045 | |||||||
| chr22:29227394 | C | CTT | 15 | a0001c0001t0001g0031 a0001c0001t0001g0292 a0001c0001t0002g0023 others(12): Show |
15 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.465+856_465+857dup others(2): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29227394 | ||||||
| chr22:29227409 | A | G | 1 | a0002c0002t0003g0341 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.465+858A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227409 | |||||||
| chr22:29227414 | A | G | 1 | a0002c0008t0002g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.465+863A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227414 | |||||||
| chr22:29227436 | G | A | 1 | a0002c0002t0003g0257 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.465+885G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227436 | |||||||
| chr22:29227449 | A | G | 13 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0176 others(10): Show |
13 | HG00558.hp1 HG00609.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.465+898A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227449 | |||||||
| chr22:29227478 | G | A | 1 | a0003c0003t0001g0318 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.465+927G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227478 | |||||||
| chr22:29227704 | C | CA | 7 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0001t0001g0260 others(4): Show |
7 | HG00544.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.465+1176dupA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29227704 | ||||||
| chr22:29227704 | CA | C | 52 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(49): Show |
54 | HG00099.hp1 HG00280.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.465+1176delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29227704 | ||||||
| chr22:29227704 | CAA | C | 86 | a0001c0001t0001g0031 a0001c0001t0001g0050 a0001c0001t0001g0066 others(83): Show |
87 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.465+1175_465+1176d others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29227704 | ||||||
| chr22:29227704 | CAAA | C | 21 | a0001c0001t0001g0041 a0001c0001t0001g0058 a0001c0001t0001g0082 others(18): Show |
21 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.465+1174_465+1176d others(5): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29227704 | ||||||
| chr22:29227725 | A | AAC | 7 | a0001c0001t0001g0092 a0001c0001t0001g0294 a0002c0002t0001g0093 others(4): Show |
7 | HG00558.hp1 HG00609.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.465+1175_465+1176i others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29227725 | ||||||
| chr22:29227725 | A | AC | 37 | a0001c0001t0001g0072 a0001c0001t0001g0135 a0001c0001t0001g0176 others(34): Show |
38 | HG01346.hp1 HG01891.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.465+1174_465+1175i others(3): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227725 | |||||||
| chr22:29227725 | A | C | 117 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(114): Show |
119 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.465+1174A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227725 | |||||||
| chr22:29227782 | G | A | 1 | a0003c0003t0003g0208 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.465+1231G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227782 | |||||||
| chr22:29227786 | C | T | 1 | a0002c0002t0002g0195 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.465+1235C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227786 | |||||||
| chr22:29227839 | C | A | 3 | a0003c0003t0001g0331 a0003c0003t0001g0332 a0003c0003t0001g0333 |
3 | HG02258.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.465+1288C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227839 | |||||||
| chr22:29227859 | C | G | 5 | a0002c0002t0002g0034 a0002c0002t0002g0036 a0003c0003t0001g0331 others(2): Show |
5 | HG02258.hp1 HG02486.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+1308C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227859 | |||||||
| chr22:29227871 | C | T | 4 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0160 others(1): Show |
4 | HG00408.hp1 HG00438.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+1320C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227871 | |||||||
| chr22:29227930 | C | T | 3 | a0001c0001t0001g0255 a0002c0002t0001g0253 a0002c0002t0001g0254 |
3 | HG02683.hp2 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.465+1379C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227930 | |||||||
| chr22:29227931 | G | A | 1 | a0003c0003t0003g0290 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.465+1380G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227931 | |||||||
| chr22:29227970 | A | G | 2 | a0001c0001t0001g0031 a0002c0002t0002g0197 |
2 | HG01496.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.465+1419A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227970 | |||||||
| chr22:29227994 | A | G | 106 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(103): Show |
108 | HG00280.hp1 HG00558.hp1 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.465+1443A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227994 | |||||||
| chr22:29228051 | G | A | 20 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0274 others(17): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.465+1500G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228051 | |||||||
| chr22:29228104 | C | T | 1 | a0003c0003t0001g0210 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.465+1553C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228104 | |||||||
| chr22:29228150 | C | T | 3 | a0001c0001t0003g0230 a0002c0002t0003g0004 a0002c0002t0003g0214 |
4 | NA18747.hp1 NA18964.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+1599C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228150 | |||||||
| chr22:29228156 | C | CA | 49 | a0001c0001t0001g0007 a0001c0001t0001g0072 a0001c0001t0001g0092 others(46): Show |
51 | HG00558.hp1 HG00609.hp1 HG01192.hp1 others(48): Show |
intron_variant | MODIFIER | c.465+1626dupA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29228156 | ||||||
| chr22:29228156 | C | CAA | 10 | a0001c0001t0001g0263 a0001c0001t0001g0272 a0001c0001t0002g0167 others(7): Show |
10 | HG03017.hp2 HG03491.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.465+1625_465+1626d others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29228156 | ||||||
| chr22:29228156 | CA | C | 13 | a0001c0001t0001g0080 a0001c0001t0001g0166 a0001c0001t0001g0171 others(10): Show |
13 | HG00733.hp1 HG01070.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.465+1626delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29228156 | ||||||
| chr22:29228178 | T | A | 1 | a0001c0001t0002g0293 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.465+1627T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228178 | |||||||
| chr22:29228329 | A | G | 2 | a0001c0001t0001g0339 a0002c0002t0001g0126 |
2 | HG02148.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.465+1778A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228329 | |||||||
| chr22:29228593 | T | C | 45 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(42): Show |
46 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.465+2042T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228593 | |||||||
| chr22:29228856 | G | A | 1 | a0002c0002t0001g0303 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.466-2164G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228856 | |||||||
| chr22:29228892 | A | T | 51 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(48): Show |
52 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(49): Show |
intron_variant | MODIFIER | c.466-2128A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228892 | |||||||
| chr22:29228898 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.466-2122G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228898 | |||||||
| chr22:29229077 | C | T | 1 | a0002c0002t0001g0303 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.466-1943C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229077 | |||||||
| chr22:29229278 | G | A | 1 | a0002c0002t0003g0341 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.466-1742G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229278 | |||||||
| chr22:29229310 | G | T | 3 | a0003c0003t0003g0017 a0003c0003t0003g0018 a0004c0004t0003g0304 |
3 | HG02886.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.466-1710G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229310 | |||||||
| chr22:29229318 | G | A | 5 | a0001c0001t0001g0310 a0001c0001t0003g0334 a0001c0001t0003g0335 others(2): Show |
5 | HG02257.hp1 HG02572.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-1702G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229318 | |||||||
| chr22:29229369 | C | T | 1 | a0002c0002t0002g0014 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.466-1651C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229369 | |||||||
| chr22:29229643 | C | CA | 100 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(97): Show |
102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.466-1361dupA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29229643 | ||||||
| chr22:29229643 | CA | C | 7 | a0001c0001t0001g0158 a0002c0002t0002g0107 a0003c0003t0003g0018 others(4): Show |
7 | HG00639.hp1 HG01175.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.466-1361delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29229643 | ||||||
| chr22:29229657 | A | G | 2 | a0002c0002t0002g0315 a0002c0002t0003g0314 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.466-1363A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229657 | |||||||
| chr22:29229917 | C | T | 1 | a0002c0002t0002g0014 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.466-1103C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229917 | |||||||
| chr22:29229922 | G | A | 205 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(202): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.466-1098G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229922 | |||||||
| chr22:29229957 | T | C | 1 | a0001c0001t0001g0340 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.466-1063T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229957 | |||||||
| chr22:29230091 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.466-929G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230091 | |||||||
| chr22:29230201 | C | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0274 others(17): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.466-819C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230201 | |||||||
| chr22:29230336 | GA | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(174): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.466-672delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29230336 | ||||||
| chr22:29230338 | A | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.466-682A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230338 | |||||||
| chr22:29230342 | A | C | 2 | a0001c0001t0002g0104 a0002c0009t0001g0279 |
2 | NA19043.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.466-678A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230342 | |||||||
| chr22:29230347 | A | C | 5 | a0003c0003t0002g0087 a0003c0003t0003g0069 a0003c0003t0003g0086 others(2): Show |
5 | NA18945.hp1 NA18947.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-673A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230347 | |||||||
| chr22:29230348 | A | C | 1 | a0003c0003t0002g0319 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.466-672A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230348 | |||||||
| chr22:29230525 | C | T | 1 | a0002c0002t0001g0303 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.466-495C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230525 | |||||||
| chr22:29230526 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0274 a0001c0001t0001g0340 others(2): Show |
6 | HG00099.hp1 HG01074.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-494G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230526 | |||||||
| chr22:29230624 | C | T | 205 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(202): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.466-396C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230624 | |||||||
| chr22:29230794 | A | T | 1 | a0002c0002t0003g0341 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.466-226A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230794 | |||||||
| chr22:29230804 | A | T | 54 | a0002c0002t0001g0032 a0002c0002t0001g0303 a0002c0002t0003g0341 others(51): Show |
55 | HG00438.hp1 HG00639.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.466-216A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230804 | |||||||
| chr22:29230813 | A | G | 186 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(183): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.466-207A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230813 | |||||||
| chr22:29230871 | G | A | 50 | a0003c0003t0001g0030 a0003c0003t0001g0210 a0003c0003t0001g0224 others(47): Show |
51 | HG00438.hp1 HG00639.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.466-149G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230871 | |||||||
| chr22:29230885 | G | A | 1 | a0002c0002t0003g0341 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.466-135G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230885 | |||||||
| chr22:29230904 | G | A | 1 | a0002c0002t0001g0303 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.466-116G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230904 | |||||||
| chr22:29230926 | G | A | 1 | a0002c0002t0001g0245 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.466-94G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230926 | |||||||
| chr22:29231000 | G | A | 1 | a0002c0002t0001g0188 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.466-20G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29231000 | |||||||
| chr22:29231298 | C | T | 4 | a0003c0003t0002g0042 a0003c0003t0003g0060 a0003c0003t0003g0258 others(1): Show |
4 | HG00438.hp1 HG02015.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+158C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231298 | |||||||
| chr22:29231349 | G | C | 2 | a0001c0001t0003g0217 a0001c0001t0003g0239 |
2 | HG00280.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.586+209G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231349 | |||||||
| chr22:29231441 | T | A | 1 | a0002c0002t0001g0313 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.587-152T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231441 | |||||||
| chr22:29231442 | AC | A | 41 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0176 others(38): Show |
41 | HG00558.hp1 HG00609.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.587-143delC | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr22 | 29231442 | ||||||
| chr22:29231448 | C | T | 1 | a0002c0002t0003g0179 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.587-145C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231448 | |||||||
| chr22:29231450 | C | G | 4 | a0002c0002t0001g0032 a0002c0002t0001g0303 a0002c0002t0003g0341 others(1): Show |
4 | HG01099.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-143C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231450 | |||||||
| chr22:29231462 | G | C | 3 | a0001c0001t0001g0255 a0002c0002t0001g0253 a0002c0002t0001g0254 |
3 | HG02683.hp2 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.587-131G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231462 | |||||||
| chr22:29231502 | C | T | 1 | a0002c0002t0002g0014 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.587-91C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231502 | |||||||
| chr22:29231543 | G | T | 2 | a0002c0002t0001g0303 a0002c0009t0001g0279 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.587-50G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231543 | |||||||
| chr22:29231547 | C | G | 20 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0274 others(17): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.587-46C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231547 | |||||||
| chr22:29231588 | C | G | 5 | a0002c0002t0002g0034 a0002c0002t0002g0036 a0003c0003t0001g0331 others(2): Show |
5 | HG02258.hp1 HG02486.hp1 HG03225.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.587-5C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231588 | |||||||
| chr22:29231888 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.676+206C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 7/14 | chr22 | 29231888 | |||||||
| chr22:29231955 | C | G | 6 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(3): Show |
7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.676+273C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 7/14 | chr22 | 29231955 | |||||||
| chr22:29232107 | C | G | 137 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0076 others(134): Show |
139 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.677-149C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 7/14 | chr22 | 29232107 | |||||||
| chr22:29232195 | A | G | 2 | a0002c0002t0001g0299 a0002c0002t0001g0300 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.677-61A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 7/14 | chr22 | 29232195 | |||||||
| chr22:29232233 | A | G | 1 | a0002c0002t0001g0283 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.677-23A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 7/14 | chr22 | 29232233 | |||||||
| chr22:29232542 | C | T | 2 | a0001c0001t0002g0056 a0001c0001t0002g0071 |
2 | HG03490.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.823+140C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29232542 | |||||||
| chr22:29232626 | G | A | 135 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0076 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.823+224G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29232626 | |||||||
| chr22:29232681 | G | C | 5 | a0003c0003t0001g0030 a0003c0003t0001g0316 a0003c0003t0001g0317 others(2): Show |
5 | HG01496.hp1 HG02055.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+279G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29232681 | |||||||
| chr22:29232703 | T | G | 1 | a0002c0002t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.823+301T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29232703 | |||||||
| chr22:29232752 | C | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(29): Show |
33 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.823+350C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29232752 | |||||||
| chr22:29232817 | G | A | 56 | a0003c0003t0001g0030 a0003c0003t0001g0210 a0003c0003t0001g0224 others(53): Show |
57 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.823+415G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29232817 | |||||||
| chr22:29232909 | TCTC | T | 8 | a0001c0001t0001g0282 a0002c0002t0001g0188 a0002c0002t0001g0189 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.824-468_824-466del others(3): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 29232909 | ||||||
| chr22:29233024 | G | C | 4 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0140 others(1): Show |
4 | HG00733.hp2 HG01070.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-355G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29233024 | |||||||
| chr22:29233174 | G | T | 1 | a0002c0002t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.824-205G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29233174 | |||||||
| chr22:29233240 | G | T | 2 | a0001c0001t0001g0252 a0002c0002t0002g0256 |
2 | NA18959.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.824-139G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29233240 | |||||||
| chr22:29233737 | C | T | 9 | a0001c0001t0001g0242 a0001c0001t0001g0252 a0001c0001t0002g0114 others(6): Show |
9 | NA18948.hp1 NA18959.hp1 NA18977.hp2 others(6): Show |
intron_variant | MODIFIER | c.966+71C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 10/14 | chr22 | 29233737 | |||||||
| chr22:29234226 | G | A | 1 | a0002c0002t0001g0298 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1029+27G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 11/14 | chr22 | 29234226 | |||||||
| chr22:29234280 | C | T | 1 | a0002c0002t0001g0338 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1030-25C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 11/14 | chr22 | 29234280 | |||||||
| chr22:29234292 | C | T | 1 | a0002c0002t0001g0016 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1030-13C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 11/14 | chr22 | 29234292 | |||||||
| chr22:29234360 | C | T | 2 | a0003c0003t0001g0030 a0003c0003t0001g0318 |
2 | HG01496.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1074+11C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29234360 | |||||||
| chr22:29234509 | T | C | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1074+160T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29234509 | |||||||
| chr22:29234575 | C | T | 297 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0031 others(294): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1074+226C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29234575 | |||||||
| chr22:29234633 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1074+284G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29234633 | |||||||
| chr22:29234833 | C | G | 292 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0031 others(289): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1074+484C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29234833 | |||||||
| chr22:29234902 | A | G | 42 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(39): Show |
43 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1074+553A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29234902 | |||||||
| chr22:29234995 | G | A | 1 | a0002c0002t0002g0015 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1074+646G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29234995 | |||||||
| chr22:29235046 | A | T | 1 | a0002c0009t0001g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1074+697A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29235046 | |||||||
| chr22:29235103 | T | C | 67 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0072 others(64): Show |
70 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1074+754T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29235103 | |||||||
| chr22:29235158 | G | A | 1 | a0002c0002t0001g0110 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1074+809G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29235158 | |||||||
| chr22:29235348 | C | CA | 10 | a0001c0001t0001g0112 a0001c0001t0003g0130 a0001c0001t0003g0131 others(7): Show |
10 | HG00741.hp2 HG01099.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1074+1019dupA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235348 | ||||||
| chr22:29235348 | CA | C | 26 | a0001c0001t0001g0010 a0001c0001t0001g0147 a0001c0001t0001g0152 others(23): Show |
26 | HG00099.hp2 HG00408.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1074+1019delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235348 | ||||||
| chr22:29235348 | CAA | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(85): Show |
90 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1074+1018_1074+101 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235348 | ||||||
| chr22:29235348 | CAAA | C | 61 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0072 others(58): Show |
63 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.1074+1017_1074+101 others(7): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235348 | ||||||
| chr22:29235616 | A | G | 3 | a0001c0001t0001g0070 a0001c0001t0001g0091 a0002c0002t0002g0221 |
3 | HG01192.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1074+1267A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29235616 | |||||||
| chr22:29235780 | C | CT | 64 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0051 others(61): Show |
64 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1074+1458dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235780 | ||||||
| chr22:29235780 | C | CTT | 12 | a0001c0001t0001g0242 a0001c0001t0001g0252 a0001c0001t0001g0255 others(9): Show |
12 | HG00741.hp2 HG02071.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.1074+1457_1074+145 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235780 | ||||||
| chr22:29235780 | CT | C | 10 | a0001c0001t0002g0056 a0002c0002t0001g0237 a0002c0002t0001g0266 others(7): Show |
10 | HG01167.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1074+1458delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235780 | ||||||
| chr22:29235780 | CTT | C | 24 | a0001c0001t0001g0031 a0001c0001t0001g0274 a0001c0001t0001g0292 others(21): Show |
25 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1074+1457_1074+145 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235780 | ||||||
| chr22:29235780 | CTTT | C | 48 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(45): Show |
49 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1074+1456_1074+145 others(7): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235780 | ||||||
| chr22:29235780 | CTTTT | C | 20 | a0001c0001t0001g0012 a0001c0001t0001g0294 a0001c0001t0002g0167 others(17): Show |
20 | HG00741.hp1 HG01081.hp2 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1074+1455_1074+145 others(8): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235780 | ||||||
| chr22:29235780 | CTTTTT | C | 47 | a0003c0003t0001g0030 a0003c0003t0001g0210 a0003c0003t0001g0316 others(44): Show |
48 | HG00438.hp1 HG00639.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.1074+1454_1074+145 others(9): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235780 | ||||||
| chr22:29235793 | T | C | 6 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(3): Show |
7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1074+1444T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29235793 | |||||||
| chr22:29235814 | G | T | 1 | a0002c0002t0006g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1074+1465G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29235814 | |||||||
| chr22:29236063 | A | T | 1 | a0001c0001t0001g0242 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1074+1714A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236063 | |||||||
| chr22:29236122 | A | G | 1 | a0002c0002t0001g0237 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1074+1773A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236122 | |||||||
| chr22:29236269 | A | C | 92 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(89): Show |
94 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1074+1920A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236269 | |||||||
| chr22:29236407 | T | C | 23 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(20): Show |
24 | HG00558.hp1 HG00609.hp1 HG02080.hp1 others(21): Show |
intron_variant | MODIFIER | c.1074+2058T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236407 | |||||||
| chr22:29236418 | C | T | 35 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0176 others(32): Show |
35 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.1074+2069C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236418 | |||||||
| chr22:29236465 | G | T | 1 | a0002c0002t0001g0143 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1074+2116G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236465 | |||||||
| chr22:29236506 | C | T | 3 | a0003c0003t0001g0331 a0003c0003t0001g0332 a0003c0003t0001g0333 |
3 | HG02258.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1074+2157C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236506 | |||||||
| chr22:29236519 | C | T | 7 | a0001c0001t0001g0157 a0001c0001t0001g0325 a0001c0001t0001g0328 others(4): Show |
7 | HG00280.hp1 HG02698.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.1074+2170C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236519 | |||||||
| chr22:29236568 | G | A | 200 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0043 others(197): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.1074+2219G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236568 | |||||||
| chr22:29236607 | C | T | 125 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0076 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1074+2258C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236607 | |||||||
| chr22:29236742 | T | C | 59 | a0003c0003t0001g0030 a0003c0003t0001g0210 a0003c0003t0001g0224 others(56): Show |
60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1074+2393T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236742 | |||||||
| chr22:29236749 | A | G | 32 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(29): Show |
33 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.1074+2400A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236749 | |||||||
| chr22:29236798 | T | C | 7 | a0002c0002t0001g0016 a0002c0002t0001g0313 a0002c0002t0002g0015 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074+2449T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236798 | |||||||
| chr22:29236837 | C | T | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1074+2488C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236837 | |||||||
| chr22:29236883 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1074+2534G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236883 | |||||||
| chr22:29236893 | A | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(30): Show |
34 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.1074+2544A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236893 | |||||||
| chr22:29237040 | C | T | 1 | a0003c0003t0003g0005 | 2 | NA18969.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1074+2691C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237040 | |||||||
| chr22:29237041 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1074+2692G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237041 | |||||||
| chr22:29237070 | C | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(89): Show |
94 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1074+2721C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237070 | |||||||
| chr22:29237086 | C | G | 91 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(88): Show |
93 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1074+2737C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237086 | |||||||
| chr22:29237097 | TATTTTCT others(2297): Show |
T | 69 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0072 others(66): Show |
72 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1074+2752_1075-404 others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29237097 | ||||||
| chr22:29237245 | T | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(88): Show |
93 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1074+2896T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237245 | |||||||
| chr22:29237378 | A | G | 1 | a0001c0001t0003g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1074+3029A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237378 | |||||||
| chr22:29237499 | T | C | 1 | a0002c0009t0001g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1074+3150T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237499 | |||||||
| chr22:29237615 | G | A | 1 | a0002c0002t0001g0237 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1074+3266G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237615 | |||||||
| chr22:29237800 | C | CA | 127 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0076 others(124): Show |
128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1074+3459dupA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29237800 | ||||||
| chr22:29237800 | C | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01081.hp2 HG01109.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1074+3451C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237800 | |||||||
| chr22:29237837 | C | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(89): Show |
94 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1074+3488C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237837 | |||||||
| chr22:29237907 | C | T | 6 | a0001c0001t0003g0047 a0001c0001t0003g0217 a0001c0001t0003g0239 others(3): Show |
6 | HG00280.hp2 HG02132.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+3558C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237907 | |||||||
| chr22:29237946 | G | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(29): Show |
33 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.1074+3597G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237946 | |||||||
| chr22:29238154 | G | C | 1 | a0002c0002t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1074+3805G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238154 | |||||||
| chr22:29238254 | A | AATT | 10 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0162 others(7): Show |
10 | HG00438.hp2 HG01515.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1074+3952_1074+395 others(7): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238254 | ||||||
| chr22:29238254 | AATT | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(51): Show |
54 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1074+3952_1074+395 others(7): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238254 | ||||||
| chr22:29238254 | AATTATT | A | 26 | a0001c0001t0001g0154 a0001c0001t0001g0282 a0001c0001t0001g0291 others(23): Show |
26 | HG00642.hp2 HG01070.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.1074+3949_1074+395 others(10): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238254 | ||||||
| chr22:29238254 | AATTATTA others(2): Show |
A | 50 | a0001c0001t0001g0070 a0001c0001t0001g0091 a0001c0001t0001g0094 others(47): Show |
51 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1074+3946_1074+395 others(13): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238254 | ||||||
| chr22:29238254 | AATTATTA others(5): Show |
A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(14): Show |
17 | HG01081.hp2 HG01099.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1074+3943_1074+395 others(16): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238254 | ||||||
| chr22:29238254 | AATTATTA others(8): Show |
A | 2 | a0002c0002t0001g0054 a0002c0008t0002g0049 |
2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1074+3940_1074+395 others(19): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238254 | ||||||
| chr22:29238254 | AATTATTA others(14): Show |
A | 3 | a0002c0002t0002g0193 a0002c0002t0002g0194 a0002c0002t0002g0195 |
3 | NA18955.hp2 NA19005.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1074+3934_1074+395 others(25): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238254 | ||||||
| chr22:29238362 | C | A | 4 | a0002c0002t0001g0211 a0002c0002t0001g0212 a0002c0002t0001g0299 others(1): Show |
4 | HG03139.hp2 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+4013C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238362 | |||||||
| chr22:29238424 | T | C | 56 | a0002c0002t0002g0192 a0003c0003t0001g0030 a0003c0003t0001g0210 others(53): Show |
57 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1074+4075T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238424 | |||||||
| chr22:29238489 | C | G | 1 | a0002c0002t0001g0245 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1074+4140C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238489 | |||||||
| chr22:29238513 | G | A | 49 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0077 others(46): Show |
49 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.1074+4164G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238513 | |||||||
| chr22:29238715 | G | A | 130 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0076 others(127): Show |
131 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.1074+4366G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238715 | |||||||
| chr22:29238719 | AT | A | 64 | a0001c0001t0001g0273 a0001c0001t0002g0251 a0002c0002t0001g0032 others(61): Show |
65 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1074+4390delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238719 | ||||||
| chr22:29238719 | ATT | A | 125 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0076 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1074+4389_1074+439 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238719 | ||||||
| chr22:29238739 | T | A | 1 | a0001c0001t0001g0267 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1074+4390T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238739 | |||||||
| chr22:29238778 | G | T | 59 | a0002c0002t0002g0192 a0003c0003t0001g0030 a0003c0003t0001g0210 others(56): Show |
60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1074+4429G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238778 | |||||||
| chr22:29239299 | AT | A | 129 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0076 others(126): Show |
130 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1075-4137delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29239299 | ||||||
| chr22:29239300 | T | A | 1 | a0001c0001t0002g0149 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1075-4145T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239300 | |||||||
| chr22:29239322 | G | A | 130 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0076 others(127): Show |
131 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.1075-4123G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239322 | |||||||
| chr22:29239323 | G | T | 2 | a0002c0002t0001g0032 a0002c0009t0001g0279 |
2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1075-4122G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239323 | |||||||
| chr22:29239413 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1075-4032G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239413 | |||||||
| chr22:29239430 | C | T | 198 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0043 others(195): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1075-4015C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239430 | |||||||
| chr22:29239456 | C | T | 1 | a0004c0004t0003g0219 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1075-3989C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239456 | |||||||
| chr22:29239468 | C | A | 1 | a0004c0004t0003g0120 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1075-3977C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239468 | |||||||
| chr22:29239692 | C | G | 1 | a0002c0002t0002g0240 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1075-3753C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239692 | |||||||
| chr22:29239745 | A | G | 1 | a0003c0003t0003g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1075-3700A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239745 | |||||||
| chr22:29239761 | C | CT | 37 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(34): Show |
38 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1075-3670dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29239761 | ||||||
| chr22:29239786 | C | G | 1 | a0006c0006t0003g0068 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1075-3659C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239786 | |||||||
| chr22:29239869 | C | T | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1075-3576C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239869 | |||||||
| chr22:29239873 | CATCAACC others(45): Show |
C | 59 | a0002c0002t0002g0192 a0003c0003t0001g0030 a0003c0003t0001g0210 others(56): Show |
60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1075-3537_1075-348 others(56): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29239873 | ||||||
| chr22:29239879 | C | T | 6 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(3): Show |
7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-3566C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239879 | |||||||
| chr22:29239904 | C | T | 1 | a0002c0002t0001g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1075-3541C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239904 | |||||||
| chr22:29240013 | G | A | 198 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0043 others(195): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1075-3432G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240013 | |||||||
| chr22:29240121 | A | G | 3 | a0001c0001t0001g0070 a0001c0001t0001g0091 a0002c0002t0002g0221 |
3 | HG01192.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1075-3324A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240121 | |||||||
| chr22:29240152 | T | A | 198 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0043 others(195): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1075-3293T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240152 | |||||||
| chr22:29240274 | T | C | 1 | a0001c0001t0002g0244 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1075-3171T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240274 | |||||||
| chr22:29240394 | AAG | A | 127 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0076 others(124): Show |
128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1075-3048_1075-304 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29240394 | ||||||
| chr22:29240397 | A | G | 1 | a0002c0002t0003g0057 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1075-3048A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240397 | |||||||
| chr22:29240567 | G | C | 4 | a0002c0002t0001g0211 a0002c0002t0001g0212 a0002c0002t0001g0299 others(1): Show |
4 | HG03139.hp2 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1075-2878G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240567 | |||||||
| chr22:29240692 | G | A | 6 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(3): Show |
7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-2753G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240692 | |||||||
| chr22:29240724 | T | A | 62 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0002t0003g0341 others(59): Show |
63 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1075-2721T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240724 | |||||||
| chr22:29240767 | G | A | 2 | a0002c0002t0001g0032 a0002c0009t0001g0279 |
2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1075-2678G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240767 | |||||||
| chr22:29240841 | T | C | 62 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0002t0003g0341 others(59): Show |
63 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1075-2604T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240841 | |||||||
| chr22:29240852 | A | T | 7 | a0001c0001t0001g0282 a0002c0002t0001g0188 a0002c0002t0001g0189 others(4): Show |
7 | HG02109.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-2593A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240852 | |||||||
| chr22:29240879 | G | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0036 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1075-2566G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240879 | |||||||
| chr22:29240884 | C | A | 1 | a0001c0001t0001g0135 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1075-2561C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240884 | |||||||
| chr22:29240996 | C | T | 59 | a0002c0002t0002g0192 a0003c0003t0001g0030 a0003c0003t0001g0210 others(56): Show |
60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1075-2449C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240996 | |||||||
| chr22:29241104 | C | CTA | 62 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0002t0003g0341 others(59): Show |
63 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1075-2340_1075-233 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29241104 | ||||||
| chr22:29241150 | T | G | 8 | a0001c0001t0001g0112 a0001c0001t0001g0153 a0001c0001t0001g0154 others(5): Show |
8 | NA18612.hp1 NA18942.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.1075-2295T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241150 | |||||||
| chr22:29241255 | T | C | 46 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(43): Show |
47 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(44): Show |
intron_variant | MODIFIER | c.1075-2190T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241255 | |||||||
| chr22:29241292 | G | T | 6 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(3): Show |
7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-2153G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241292 | |||||||
| chr22:29241361 | CTTG | C | 6 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(3): Show |
7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-2078_1075-207 others(7): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29241361 | ||||||
| chr22:29241568 | T | G | 7 | a0003c0003t0003g0090 a0004c0004t0002g0145 a0004c0004t0003g0105 others(4): Show |
7 | NA18940.hp1 NA18944.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-1877T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241568 | |||||||
| chr22:29241578 | G | GA | 59 | a0002c0002t0002g0192 a0003c0003t0001g0030 a0003c0003t0001g0210 others(56): Show |
60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1075-1867_1075-186 others(5): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241578 | |||||||
| chr22:29241622 | C | T | 1 | a0002c0002t0002g0286 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1075-1823C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241622 | |||||||
| chr22:29241631 | C | T | 3 | a0002c0002t0002g0200 a0002c0002t0002g0301 a0002c0002t0002g0302 |
3 | HG01243.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1075-1814C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241631 | |||||||
| chr22:29241635 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0031 others(46): Show |
51 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.1075-1810C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241635 | |||||||
| chr22:29241636 | G | A | 82 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(79): Show |
83 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.1075-1809G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241636 | |||||||
| chr22:29241669 | G | C | 32 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(29): Show |
33 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.1075-1776G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241669 | |||||||
| chr22:29241793 | A | AT | 49 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0031 others(46): Show |
51 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.1075-1645dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29241793 | ||||||
| chr22:29241899 | G | A | 2 | a0002c0002t0001g0266 a0002c0002t0002g0269 |
2 | HG02602.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1075-1546G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241899 | |||||||
| chr22:29241950 | A | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0031 others(158): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1075-1495A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241950 | |||||||
| chr22:29242028 | A | G | 1 | a0006c0006t0003g0068 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1075-1417A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29242028 | |||||||
| chr22:29242220 | C | T | 2 | a0002c0002t0002g0096 a0002c0002t0002g0225 |
2 | HG00741.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1075-1225C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29242220 | |||||||
| chr22:29242398 | A | T | 62 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0002t0003g0341 others(59): Show |
63 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1075-1047A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29242398 | |||||||
| chr22:29242481 | G | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(25): Show |
29 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.1075-964G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29242481 | |||||||
| chr22:29242507 | A | G | 1 | a0002c0002t0003g0341 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1075-938A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29242507 | |||||||
| chr22:29243015 | C | A | 1 | a0002c0002t0002g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1075-430C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243015 | |||||||
| chr22:29243047 | C | T | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1075-398C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243047 | |||||||
| chr22:29243072 | C | T | 1 | a0002c0002t0003g0142 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1075-373C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243072 | |||||||
| chr22:29243101 | C | T | 59 | a0002c0002t0002g0192 a0003c0003t0001g0030 a0003c0003t0001g0210 others(56): Show |
60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1075-344C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243101 | |||||||
| chr22:29243126 | T | C | 1 | a0002c0002t0002g0201 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1075-319T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243126 | |||||||
| chr22:29243146 | CT | C | 161 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0031 others(158): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1075-297delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29243146 | ||||||
| chr22:29243172 | A | G | 60 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0003c0003t0001g0030 others(57): Show |
61 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.1075-273A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243172 | |||||||
| chr22:29243203 | C | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0031 others(158): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1075-242C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243203 | |||||||
| chr22:29243389 | G | A | 6 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(3): Show |
7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-56G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243389 | |||||||
| chr22:29243725 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1119+236C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29243725 | |||||||
| chr22:29243838 | A | G | 1 | a0001c0001t0002g0284 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1119+349A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29243838 | |||||||
| chr22:29243960 | G | A | 1 | a0002c0002t0001g0246 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1119+471G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29243960 | |||||||
| chr22:29244013 | A | G | 4 | a0003c0003t0005g0280 a0003c0003t0005g0281 a0003c0003t0005g0320 others(1): Show |
4 | HG02145.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+524A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244013 | |||||||
| chr22:29244030 | C | T | 59 | a0002c0002t0002g0192 a0003c0003t0001g0030 a0003c0003t0001g0210 others(56): Show |
60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1119+541C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244030 | |||||||
| chr22:29244245 | A | G | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1119+756A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244245 | |||||||
| chr22:29244262 | C | T | 4 | a0003c0003t0001g0030 a0003c0003t0001g0316 a0003c0003t0001g0317 others(1): Show |
4 | HG01496.hp1 HG02055.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+773C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244262 | |||||||
| chr22:29244320 | G | A | 60 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0003c0003t0001g0030 others(57): Show |
61 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.1119+831G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244320 | |||||||
| chr22:29244378 | G | T | 6 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(3): Show |
7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119+889G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244378 | |||||||
| chr22:29244383 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1119+894G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244383 | |||||||
| chr22:29244524 | A | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0031 others(46): Show |
51 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.1119+1035A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244524 | |||||||
| chr22:29244650 | AAG | A | 47 | a0003c0003t0001g0030 a0003c0003t0001g0210 a0003c0003t0001g0224 others(44): Show |
48 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.1119+1163_1119+116 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29244650 | ||||||
| chr22:29244651 | AG | A | 11 | a0002c0002t0002g0192 a0003c0003t0001g0331 a0003c0003t0003g0018 others(8): Show |
11 | HG01884.hp2 HG02258.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1119+1163delG | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244651 | |||||||
| chr22:29244657 | G | A | 61 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0009t0001g0279 others(58): Show |
62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1168G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244657 | |||||||
| chr22:29244662 | G | A | 61 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0009t0001g0279 others(58): Show |
62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1173G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244662 | |||||||
| chr22:29244667 | T | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): Show |
31 | HG01081.hp2 HG01099.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1119+1178T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244667 | |||||||
| chr22:29244667 | T | G | 61 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0009t0001g0279 others(58): Show |
62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1178T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244667 | |||||||
| chr22:29244716 | G | A | 37 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0041 others(34): Show |
39 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(36): Show |
intron_variant | MODIFIER | c.1119+1227G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244716 | |||||||
| chr22:29244731 | T | A | 61 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0009t0001g0279 others(58): Show |
62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1242T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244731 | |||||||
| chr22:29244748 | C | T | 6 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(3): Show |
7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119+1259C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244748 | |||||||
| chr22:29244757 | A | AAGACG | 37 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0041 others(34): Show |
39 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(36): Show |
intron_variant | MODIFIER | c.1119+1271_1119+127 others(9): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29244757 | ||||||
| chr22:29244840 | G | A | 1 | a0002c0002t0001g0020 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1119+1351G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244840 | |||||||
| chr22:29244856 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1119+1367G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244856 | |||||||
| chr22:29244912 | G | T | 1 | a0001c0001t0001g0339 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1119+1423G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244912 | |||||||
| chr22:29245029 | T | C | 61 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0009t0001g0279 others(58): Show |
62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1540T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245029 | |||||||
| chr22:29245069 | C | CT | 61 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0009t0001g0279 others(58): Show |
62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1581dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29245069 | ||||||
| chr22:29245106 | C | G | 61 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0009t0001g0279 others(58): Show |
62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1617C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245106 | |||||||
| chr22:29245188 | C | T | 1 | a0002c0002t0001g0303 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1119+1699C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245188 | |||||||
| chr22:29245189 | G | A | 2 | a0003c0003t0003g0017 a0003c0003t0003g0018 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1119+1700G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245189 | |||||||
| chr22:29245289 | A | G | 61 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0009t0001g0279 others(58): Show |
62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1800A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245289 | |||||||
| chr22:29245338 | T | C | 61 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0009t0001g0279 others(58): Show |
62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1849T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245338 | |||||||
| chr22:29245405 | C | A | 6 | a0001c0001t0002g0167 a0002c0002t0001g0173 a0002c0002t0001g0175 others(3): Show |
6 | NA18939.hp2 NA18943.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+1916C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245405 | |||||||
| chr22:29245451 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1119+1962G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245451 | |||||||
| chr22:29245479 | C | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0274 a0001c0001t0001g0340 others(2): Show |
6 | HG00099.hp1 HG01074.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+1990C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245479 | |||||||
| chr22:29245562 | T | C | 61 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0009t0001g0279 others(58): Show |
62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+2073T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245562 | |||||||
| chr22:29245566 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1119+2077G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245566 | |||||||
| chr22:29245579 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1119+2090G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245579 | |||||||
| chr22:29245672 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1119+2183T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245672 | |||||||
| chr22:29245706 | C | T | 58 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0009t0001g0279 others(55): Show |
59 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1119+2217C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245706 | |||||||
| chr22:29245750 | G | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0041 others(37): Show |
42 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.1119+2261G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245750 | |||||||
| chr22:29245752 | G | T | 56 | a0002c0002t0002g0192 a0003c0003t0001g0030 a0003c0003t0001g0210 others(53): Show |
57 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1119+2263G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245752 | |||||||
| chr22:29245758 | G | C | 7 | a0002c0002t0001g0016 a0002c0002t0001g0313 a0002c0002t0002g0015 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1119+2269G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245758 | |||||||
| chr22:29245868 | C | T | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1119+2379C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245868 | |||||||
| chr22:29245941 | C | T | 2 | a0002c0002t0001g0061 a0002c0002t0001g0062 |
2 | NA18952.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1119+2452C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245941 | |||||||
| chr22:29246008 | A | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0031 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1119+2519A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246008 | |||||||
| chr22:29246023 | A | G | 5 | a0004c0004t0001g0059 a0004c0004t0003g0073 a0004c0004t0003g0083 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119+2534A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246023 | |||||||
| chr22:29246109 | G | A | 1 | a0002c0002t0001g0313 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1119+2620G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246109 | |||||||
| chr22:29246111 | A | C | 2 | a0004c0004t0003g0215 a0004c0004t0003g0216 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1119+2622A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246111 | |||||||
| chr22:29246122 | A | G | 58 | a0002c0002t0001g0032 a0002c0002t0002g0192 a0002c0009t0001g0279 others(55): Show |
59 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1119+2633A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246122 | |||||||
| chr22:29246148 | T | C | 1 | a0002c0002t0003g0214 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1119+2659T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246148 | |||||||
| chr22:29246275 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1119+2786G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246275 | |||||||
| chr22:29246310 | A | C | 4 | a0001c0001t0002g0114 a0002c0002t0002g0127 a0002c0002t0002g0128 others(1): Show |
4 | NA18948.hp1 NA19000.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+2821A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246310 | |||||||
| chr22:29246376 | G | A | 129 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0076 others(126): Show |
130 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1119+2887G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246376 | |||||||
| chr22:29246384 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1119+2895C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246384 | |||||||
| chr22:29246394 | T | C | 3 | a0004c0004t0003g0120 a0004c0004t0003g0185 a0004c0004t0003g0209 |
3 | NA18973.hp2 NA18986.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1119+2905T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246394 | |||||||
| chr22:29246397 | C | T | 7 | a0001c0001t0001g0282 a0002c0002t0001g0188 a0002c0002t0001g0189 others(4): Show |
7 | HG02109.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1119+2908C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246397 | |||||||
| chr22:29246463 | G | C | 6 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(3): Show |
7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119+2974G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246463 | |||||||
| chr22:29246468 | G | A | 1 | a0002c0009t0001g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1119+2979G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246468 | |||||||
| chr22:29246503 | G | A | 44 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(41): Show |
45 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.1119+3014G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246503 | |||||||
| chr22:29246534 | G | C | 2 | a0002c0002t0001g0032 a0002c0009t0001g0279 |
2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1119+3045G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246534 | |||||||
| chr22:29246599 | G | A | 46 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(43): Show |
47 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(44): Show |
intron_variant | MODIFIER | c.1119+3110G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246599 | |||||||
| chr22:29246841 | C | A | 18 | a0001c0001t0001g0031 a0001c0001t0001g0292 a0001c0001t0002g0265 others(15): Show |
19 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.1119+3352C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246841 | |||||||
| chr22:29246853 | A | G | 1 | a0003c0003t0003g0296 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1119+3364A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246853 | |||||||
| chr22:29246859 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1119+3370C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246859 | |||||||
| chr22:29247096 | A | T | 2 | a0004c0004t0003g0215 a0004c0004t0003g0216 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1119+3607A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247096 | |||||||
| chr22:29247218 | G | A | 1 | a0002c0002t0003g0341 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1119+3729G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247218 | |||||||
| chr22:29247305 | A | G | 46 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(43): Show |
47 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(44): Show |
intron_variant | MODIFIER | c.1119+3816A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247305 | |||||||
| chr22:29247360 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1119+3871T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247360 | |||||||
| chr22:29247382 | C | T | 1 | a0002c0009t0001g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1119+3893C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247382 | |||||||
| chr22:29247432 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0031 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1119+3943G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247432 | |||||||
| chr22:29247532 | C | T | 7 | a0001c0001t0002g0124 a0002c0002t0001g0065 a0002c0002t0001g0099 others(4): Show |
7 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(4): Show |
intron_variant | MODIFIER | c.1119+4043C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247532 | |||||||
| chr22:29247549 | A | C | 12 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0080 others(9): Show |
12 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.1119+4060A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247549 | |||||||
| chr22:29247670 | G | A | 44 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(41): Show |
45 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.1119+4181G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247670 | |||||||
| chr22:29247787 | G | A | 6 | a0002c0002t0001g0211 a0002c0002t0001g0212 a0002c0002t0001g0298 others(3): Show |
6 | HG03130.hp1 HG03139.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+4298G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247787 | |||||||
| chr22:29247812 | G | A | 4 | a0003c0003t0005g0280 a0003c0003t0005g0281 a0003c0003t0005g0320 others(1): Show |
4 | HG02145.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+4323G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247812 | |||||||
| chr22:29247948 | CT | C | 57 | a0001c0001t0001g0080 a0002c0002t0002g0192 a0003c0003t0001g0030 others(54): Show |
58 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1119+4473delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29247948 | ||||||
| chr22:29247970 | A | G | 2 | a0002c0002t0001g0054 a0002c0008t0002g0049 |
2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1119+4481A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247970 | |||||||
| chr22:29248038 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1119+4549G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248038 | |||||||
| chr22:29248188 | A | G | 1 | a0002c0002t0001g0303 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1119+4699A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248188 | |||||||
| chr22:29248220 | A | G | 6 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(3): Show |
7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119+4731A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248220 | |||||||
| chr22:29248259 | C | CT | 23 | a0001c0001t0001g0112 a0001c0001t0001g0153 a0001c0001t0001g0154 others(20): Show |
23 | HG00423.hp2 HG00597.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1119+4791dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29248259 | ||||||
| chr22:29248259 | CT | C | 11 | a0001c0001t0001g0082 a0001c0001t0001g0282 a0001c0005t0001g0276 others(8): Show |
11 | HG01175.hp1 HG02109.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1119+4791delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29248259 | ||||||
| chr22:29248259 | CTT | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0050 others(35): Show |
39 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1119+4790_1119+479 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29248259 | ||||||
| chr22:29248259 | CTTT | C | 56 | a0001c0001t0001g0007 a0001c0001t0001g0274 a0001c0001t0001g0340 others(53): Show |
58 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1119+4789_1119+479 others(7): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29248259 | ||||||
| chr22:29248259 | CTTTT | C | 19 | a0001c0001t0001g0031 a0001c0001t0001g0176 a0001c0001t0001g0272 others(16): Show |
19 | HG01192.hp1 HG01243.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.1119+4788_1119+479 others(8): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29248259 | ||||||
| chr22:29248259 | CTTTTT | C | 45 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(42): Show |
47 | HG00558.hp1 HG00609.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.1119+4787_1119+479 others(9): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29248259 | ||||||
| chr22:29248281 | C | A | 1 | a0002c0002t0001g0118 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1119+4792C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248281 | |||||||
| chr22:29248790 | G | A | 1 | a0005c0007t0003g0187 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1119+5301G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248790 | |||||||
| chr22:29248818 | GC | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0031 others(158): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1119+5330delC | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248818 | |||||||
| chr22:29248942 | G | A | 9 | a0002c0002t0002g0045 a0002c0002t0002g0046 a0002c0002t0002g0074 others(6): Show |
9 | HG00544.hp2 NA18944.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.1120-5261G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248942 | |||||||
| chr22:29248972 | A | G | 13 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0176 others(10): Show |
13 | HG00558.hp1 HG00609.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.1120-5231A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248972 | |||||||
| chr22:29249237 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0274 a0001c0001t0001g0340 others(2): Show |
6 | HG00099.hp1 HG01074.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-4966T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249237 | |||||||
| chr22:29249246 | C | CT | 5 | a0001c0001t0001g0291 a0001c0001t0002g0293 a0001c0001t0002g0307 others(2): Show |
5 | HG01070.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120-4949dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249246 | ||||||
| chr22:29249258 | A | G | 5 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(2): Show |
6 | HG01884.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-4945A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249258 | |||||||
| chr22:29249275 | G | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1120-4928G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249275 | |||||||
| chr22:29249338 | C | T | 1 | a0002c0002t0002g0264 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1120-4865C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249338 | |||||||
| chr22:29249386 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1120-4817G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249386 | |||||||
| chr22:29249397 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1120-4806G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249397 | |||||||
| chr22:29249411 | C | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1120-4792C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249411 | |||||||
| chr22:29249418 | G | A | 2 | a0002c0002t0004g0028 a0003c0003t0002g0323 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1120-4785G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249418 | |||||||
| chr22:29249567 | C | T | 5 | a0004c0004t0001g0059 a0004c0004t0003g0073 a0004c0004t0003g0083 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120-4636C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249567 | |||||||
| chr22:29249587 | A | ATTAT | 30 | a0001c0001t0001g0092 a0001c0001t0002g0144 a0001c0001t0002g0251 others(27): Show |
30 | HG00544.hp2 HG00609.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1120-4577_1120-457 others(8): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | ||||||
| chr22:29249587 | A | ATTATTTA others(1): Show |
6 | a0002c0002t0002g0191 a0002c0002t0002g0315 a0002c0002t0003g0196 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-4581_1120-457 others(12): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | ||||||
| chr22:29249587 | A | ATTATTTA others(5): Show |
2 | a0002c0002t0001g0303 a0005c0007t0003g0187 |
2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1120-4585_1120-457 others(16): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | ||||||
| chr22:29249587 | A | ATTTATTA others(1): Show |
17 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(14): Show |
17 | HG01081.hp2 HG01255.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1120-4614_1120-461 others(12): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | ||||||
| chr22:29249587 | A | ATTTATTA others(5): Show |
11 | a0001c0001t0001g0282 a0001c0001t0002g0006 a0001c0001t0002g0284 others(8): Show |
11 | HG01243.hp1 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1120-4614_1120-461 others(16): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | ||||||
| chr22:29249587 | A | ATTTATTA others(9): Show |
1 | a0002c0002t0003g0341 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1120-4614_1120-461 others(20): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | ||||||
| chr22:29249587 | ATTAT | A | 42 | a0001c0001t0001g0100 a0001c0001t0001g0157 a0001c0001t0001g0238 others(39): Show |
42 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.1120-4577_1120-457 others(8): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | ||||||
| chr22:29249587 | ATTATTTA others(1): Show |
A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(38): Show |
43 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(40): Show |
intron_variant | MODIFIER | c.1120-4581_1120-457 others(12): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | ||||||
| chr22:29249590 | ATTTAT | A | 6 | a0001c0001t0002g0167 a0002c0002t0001g0173 a0002c0002t0001g0175 others(3): Show |
6 | NA18939.hp2 NA18943.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-4610_1120-460 others(9): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249590 | ||||||
| chr22:29249640 | G | T | 1 | a0002c0002t0001g0254 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1120-4563G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249640 | |||||||
| chr22:29249667 | G | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1120-4536G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249667 | |||||||
| chr22:29249671 | A | G | 1 | a0002c0002t0002g0240 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1120-4532A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249671 | |||||||
| chr22:29249768 | C | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1120-4435C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249768 | |||||||
| chr22:29249787 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1120-4416G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249787 | |||||||
| chr22:29249906 | C | T | 56 | a0002c0002t0002g0192 a0003c0003t0001g0030 a0003c0003t0001g0210 others(53): Show |
57 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1120-4297C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249906 | |||||||
| chr22:29249914 | C | T | 5 | a0001c0001t0001g0135 a0001c0001t0003g0002 a0001c0001t0003g0131 others(2): Show |
6 | NA18955.hp1 NA18963.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-4289C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249914 | |||||||
| chr22:29250106 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(103): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.1120-4097A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250106 | |||||||
| chr22:29250225 | C | T | 1 | a0001c0001t0007g0161 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1120-3978C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250225 | |||||||
| chr22:29250285 | AATCAAGG others(12): Show |
A | 1 | a0002c0002t0006g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1120-3917_1120-389 others(23): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250285 | |||||||
| chr22:29250286 | A | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(158): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1120-3917A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250286 | |||||||
| chr22:29250311 | G | T | 1 | a0002c0002t0002g0203 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1120-3892G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250311 | |||||||
| chr22:29250313 | T | G | 1 | a0002c0002t0002g0203 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1120-3890T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250313 | |||||||
| chr22:29250450 | A | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1120-3753A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250450 | |||||||
| chr22:29250489 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1120-3714C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250489 | |||||||
| chr22:29250539 | G | A | 1 | a0002c0009t0001g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1120-3664G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250539 | |||||||
| chr22:29250544 | A | T | 2 | a0001c0001t0003g0130 a0002c0002t0003g0184 |
2 | NA18971.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1120-3659A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250544 | |||||||
| chr22:29250561 | C | CT | 170 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(167): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1120-3632dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250561 | ||||||
| chr22:29250624 | T | C | 1 | a0003c0003t0003g0139 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1120-3579T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250624 | |||||||
| chr22:29250630 | G | A | 1 | a0002c0002t0003g0179 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1120-3573G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250630 | |||||||
| chr22:29250733 | A | AT | 11 | a0001c0001t0001g0031 a0001c0001t0002g0265 a0001c0001t0002g0285 others(8): Show |
11 | HG00741.hp1 HG01192.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1120-3435dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | A | ATTTT | 5 | a0002c0002t0002g0033 a0002c0002t0002g0289 a0002c0002t0004g0001 others(2): Show |
6 | HG01884.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-3438_1120-343 others(8): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | A | ATTTTTTT | 17 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0080 others(14): Show |
18 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(15): Show |
intron_variant | MODIFIER | c.1120-3441_1120-343 others(11): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | A | ATTTTTTT others(1): Show |
16 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0058 others(13): Show |
17 | HG01081.hp1 HG01109.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1120-3442_1120-343 others(12): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0003g0101 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1120-3444_1120-343 others(14): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1120-3445_1120-343 others(15): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0050 a0001c0001t0002g0108 |
2 | HG01257.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1120-3446_1120-343 others(16): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0041 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1120-3447_1120-343 others(17): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | AT | A | 35 | a0001c0001t0001g0325 a0001c0001t0001g0328 a0001c0001t0002g0124 others(32): Show |
36 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1120-3435delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | ATT | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1120-3436_1120-343 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | ATTT | A | 122 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0076 others(119): Show |
123 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1120-3437_1120-343 others(7): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | ATTTT | A | 13 | a0001c0001t0001g0291 a0001c0001t0002g0055 a0001c0001t0003g0230 others(10): Show |
13 | HG00099.hp2 HG01070.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1120-3438_1120-343 others(8): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0136 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1120-3447_1120-343 others(17): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | ATTTTTTT others(7): Show |
A | 42 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(39): Show |
43 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1120-3448_1120-343 others(18): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | ATTTTTTT others(8): Show |
A | 2 | a0001c0001t0003g0132 a0002c0002t0001g0062 |
2 | NA18986.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1120-3449_1120-343 others(19): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250733 | ATTTTTTT others(9): Show |
A | 3 | a0001c0001t0001g0292 a0003c0003t0003g0060 a0003c0003t0003g0258 |
3 | HG02015.hp1 HG03209.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1120-3450_1120-343 others(20): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | ||||||
| chr22:29250818 | C | T | 1 | a0002c0002t0001g0237 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1120-3385C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250818 | |||||||
| chr22:29251053 | A | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01081.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1120-3150A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251053 | |||||||
| chr22:29251093 | T | A | 1 | a0001c0001t0001g0328 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1120-3110T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251093 | |||||||
| chr22:29251117 | C | T | 1 | a0003c0003t0003g0005 | 2 | NA18969.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1120-3086C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251117 | |||||||
| chr22:29251124 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1120-3079G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251124 | |||||||
| chr22:29251138 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1120-3065G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251138 | |||||||
| chr22:29251186 | A | G | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1120-3017A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251186 | |||||||
| chr22:29251226 | C | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(158): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1120-2977C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251226 | |||||||
| chr22:29251274 | G | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1120-2929G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251274 | |||||||
| chr22:29251333 | C | T | 4 | a0001c0001t0003g0217 a0001c0001t0003g0239 a0002c0002t0003g0218 others(1): Show |
4 | HG00280.hp2 HG02132.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120-2870C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251333 | |||||||
| chr22:29251382 | AT | A | 294 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(291): Show |
298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.1120-2805delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29251382 | ||||||
| chr22:29251382 | ATT | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0242 a0001c0001t0001g0274 others(5): Show |
9 | HG00099.hp1 HG01074.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.1120-2806_1120-280 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29251382 | ||||||
| chr22:29251490 | C | T | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1120-2713C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251490 | |||||||
| chr22:29251509 | G | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0036 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1120-2694G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251509 | |||||||
| chr22:29251795 | A | G | 165 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(162): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1120-2408A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251795 | |||||||
| chr22:29251865 | A | G | 55 | a0001c0001t0001g0238 a0002c0002t0002g0192 a0003c0003t0001g0030 others(52): Show |
56 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1120-2338A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251865 | |||||||
| chr22:29251967 | C | T | 3 | a0003c0003t0001g0331 a0003c0003t0001g0332 a0003c0003t0001g0333 |
3 | HG02258.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1120-2236C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251967 | |||||||
| chr22:29252108 | G | A | 1 | a0002c0002t0002g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1120-2095G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252108 | |||||||
| chr22:29252146 | C | T | 1 | a0002c0009t0001g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1120-2057C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252146 | |||||||
| chr22:29252176 | T | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(161): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.1120-2027T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252176 | |||||||
| chr22:29252190 | C | T | 4 | a0003c0003t0005g0280 a0003c0003t0005g0281 a0003c0003t0005g0320 others(1): Show |
4 | HG02145.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120-2013C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252190 | |||||||
| chr22:29252226 | T | A | 42 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(39): Show |
43 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1120-1977T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252226 | |||||||
| chr22:29252285 | C | T | 42 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(39): Show |
43 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1120-1918C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252285 | |||||||
| chr22:29252362 | G | T | 42 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(39): Show |
43 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1120-1841G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252362 | |||||||
| chr22:29252424 | A | G | 2 | a0002c0002t0001g0032 a0002c0009t0001g0279 |
2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1120-1779A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252424 | |||||||
| chr22:29252538 | C | G | 2 | a0002c0002t0001g0032 a0002c0009t0001g0279 |
2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1120-1665C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252538 | |||||||
| chr22:29252572 | G | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0036 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1120-1631G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252572 | |||||||
| chr22:29252583 | T | C | 12 | a0001c0001t0001g0031 a0001c0001t0001g0292 a0001c0001t0002g0265 others(9): Show |
12 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1120-1620T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252583 | |||||||
| chr22:29252615 | A | T | 54 | a0002c0002t0002g0192 a0003c0003t0001g0030 a0003c0003t0001g0210 others(51): Show |
55 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1120-1588A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252615 | |||||||
| chr22:29252717 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1120-1486C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252717 | |||||||
| chr22:29252772 | C | G | 1 | a0003c0003t0003g0220 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1120-1431C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252772 | |||||||
| chr22:29252939 | G | A | 3 | a0002c0002t0001g0303 a0002c0002t0003g0196 a0005c0007t0003g0187 |
3 | HG02451.hp2 HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1120-1264G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252939 | |||||||
| chr22:29252957 | C | T | 5 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(2): Show |
6 | HG01884.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-1246C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252957 | |||||||
| chr22:29253215 | C | T | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(161): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.1120-988C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253215 | |||||||
| chr22:29253309 | G | A | 54 | a0002c0002t0002g0192 a0003c0003t0001g0030 a0003c0003t0001g0210 others(51): Show |
55 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1120-894G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253309 | |||||||
| chr22:29253321 | G | A | 54 | a0002c0002t0002g0192 a0003c0003t0001g0030 a0003c0003t0001g0210 others(51): Show |
55 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1120-882G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253321 | |||||||
| chr22:29253353 | C | T | 42 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0135 others(39): Show |
43 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1120-850C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253353 | |||||||
| chr22:29253355 | G | T | 1 | a0002c0002t0001g0237 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1120-848G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253355 | |||||||
| chr22:29253356 | G | T | 1 | a0002c0002t0001g0237 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1120-847G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253356 | |||||||
| chr22:29253382 | A | G | 12 | a0001c0001t0001g0031 a0001c0001t0001g0292 a0001c0001t0002g0265 others(9): Show |
12 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1120-821A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253382 | |||||||
| chr22:29253389 | C | T | 1 | a0002c0002t0003g0259 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1120-814C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253389 | |||||||
| chr22:29253441 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1120-762G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253441 | |||||||
| chr22:29253466 | C | A | 12 | a0001c0001t0001g0031 a0001c0001t0001g0292 a0001c0001t0002g0265 others(9): Show |
12 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1120-737C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253466 | |||||||
| chr22:29253487 | CAGG | C | 54 | a0002c0002t0002g0192 a0003c0003t0001g0030 a0003c0003t0001g0210 others(51): Show |
55 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1120-713_1120-711d others(5): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29253487 | ||||||
| chr22:29253537 | G | A | 1 | a0002c0002t0011g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1120-666G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253537 | |||||||
| chr22:29253538 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1120-665C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253538 | |||||||
| chr22:29253592 | T | C | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1120-611T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253592 | |||||||
| chr22:29253593 | G | A | 5 | a0002c0002t0002g0033 a0002c0002t0002g0264 a0002c0002t0002g0289 others(2): Show |
6 | HG01884.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-610G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253593 | |||||||
| chr22:29253725 | C | G | 1 | a0001c0001t0001g0328 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1120-478C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253725 | |||||||
| chr22:29253726 | G | C | 1 | a0001c0001t0001g0328 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1120-477G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253726 | |||||||
| chr22:29253743 | G | C | 3 | a0003c0003t0003g0017 a0003c0003t0003g0018 a0004c0004t0003g0304 |
3 | HG02886.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1120-460G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253743 | |||||||
| chr22:29253786 | G | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(12): Show |
15 | HG01081.hp2 HG01243.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1120-417G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253786 | |||||||
| chr22:29253855 | T | G | 2 | a0002c0002t0004g0029 a0002c0002t0011g0305 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1120-348T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253855 | |||||||
| chr22:29253931 | G | A | 2 | a0002c0002t0004g0029 a0002c0002t0011g0305 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1120-272G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253931 | |||||||
| chr22:29253976 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1120-227A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253976 | |||||||
| chr22:29254135 | A | C | 1 | a0002c0002t0001g0237 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1120-68A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29254135 | |||||||
| chr22:29254137 | C | T | 3 | a0003c0003t0002g0087 a0003c0003t0003g0088 a0003c0003t0003g0208 |
3 | NA18945.hp1 NA18953.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1120-66C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29254137 | |||||||
| chr22:29254307 | C | T | 1 | a0002c0002t0003g0179 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1204+20C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254307 | |||||||
| chr22:29254469 | C | T | 180 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(177): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.1204+182C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254469 | |||||||
| chr22:29254571 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1204+284A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254571 | |||||||
| chr22:29254588 | T | A | 5 | a0001c0001t0001g0282 a0002c0002t0001g0188 a0002c0002t0001g0189 others(2): Show |
5 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1204+301T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254588 | |||||||
| chr22:29254660 | C | A | 1 | a0005c0007t0003g0187 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1204+373C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254660 | |||||||
| chr22:29254703 | A | G | 197 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(194): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1204+416A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254703 | |||||||
| chr22:29254752 | C | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(38): Show |
43 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(40): Show |
intron_variant | MODIFIER | c.1204+465C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254752 | |||||||
| chr22:29254785 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0274 a0001c0001t0001g0340 others(4): Show |
8 | HG00099.hp1 HG01074.hp1 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.1204+498C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254785 | |||||||
| chr22:29254916 | C | T | 180 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(177): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.1204+629C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254916 | |||||||
| chr22:29254990 | C | T | 1 | a0003c0003t0003g0005 | 2 | NA18969.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1204+703C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254990 | |||||||
| chr22:29254998 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0274 a0001c0001t0001g0340 others(2): Show |
6 | HG00099.hp1 HG01074.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1204+711G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254998 | |||||||
| chr22:29255004 | C | T | 27 | a0001c0001t0001g0031 a0001c0001t0001g0282 a0001c0001t0001g0292 others(24): Show |
28 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1204+717C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255004 | |||||||
| chr22:29255031 | CCTCA | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(174): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.1204+750_1204+753d others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 29255031 | ||||||
| chr22:29255116 | T | A | 1 | a0004c0004t0003g0073 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1204+829T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255116 | |||||||
| chr22:29255202 | C | T | 1 | a0002c0002t0001g0303 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1204+915C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255202 | |||||||
| chr22:29255239 | C | T | 1 | a0002c0002t0002g0107 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1204+952C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255239 | |||||||
| chr22:29255336 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1204+1049C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255336 | |||||||
| chr22:29255641 | G | A | 1 | a0002c0002t0002g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1204+1354G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255641 | |||||||
| chr22:29255660 | G | A | 1 | a0004c0004t0003g0120 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1204+1373G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255660 | |||||||
| chr22:29255788 | C | A | 1 | a0001c0001t0001g0328 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1204+1501C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255788 | |||||||
| chr22:29255984 | T | G | 1 | a0001c0001t0001g0328 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1204+1697T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255984 | |||||||
| chr22:29256077 | G | T | 1 | a0003c0003t0003g0139 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1204+1790G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256077 | |||||||
| chr22:29256116 | G | A | 4 | a0002c0002t0002g0200 a0002c0002t0002g0288 a0002c0002t0004g0028 others(1): Show |
4 | HG02717.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204+1829G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256116 | |||||||
| chr22:29256142 | A | T | 1 | a0001c0001t0001g0328 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1204+1855A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256142 | |||||||
| chr22:29256169 | G | A | 58 | a0001c0001t0001g0255 a0001c0001t0002g0053 a0001c0001t0002g0056 others(55): Show |
59 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1204+1882G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256169 | |||||||
| chr22:29256201 | G | A | 1 | a0002c0002t0002g0128 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1204+1914G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256201 | |||||||
| chr22:29256226 | A | T | 1 | a0001c0001t0001g0328 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1204+1939A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256226 | |||||||
| chr22:29256239 | G | A | 4 | a0001c0001t0003g0334 a0001c0001t0003g0335 a0001c0001t0003g0336 others(1): Show |
4 | HG02257.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204+1952G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256239 | |||||||
| chr22:29256289 | A | G | 14 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0150 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1204+2002A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256289 | |||||||
| chr22:29256347 | C | G | 1 | a0002c0002t0002g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1204+2060C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256347 | |||||||
| chr22:29256463 | C | CA | 13 | a0001c0001t0001g0082 a0001c0001t0001g0136 a0001c0001t0001g0162 others(10): Show |
13 | HG00741.hp2 HG01175.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.1204+2196dupA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 29256463 | ||||||
| chr22:29256463 | CA | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0135 a0001c0001t0001g0156 others(12): Show |
15 | HG01256.hp1 HG02080.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1204+2196delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 29256463 | ||||||
| chr22:29256463 | CAA | C | 26 | a0001c0001t0002g0024 a0001c0001t0002g0150 a0001c0001t0002g0265 others(23): Show |
27 | HG00741.hp1 HG01109.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1204+2195_1204+219 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 29256463 | ||||||
| chr22:29256466 | A | T | 1 | a0001c0001t0001g0328 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1204+2179A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256466 | |||||||
| chr22:29256664 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1205-2153C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256664 | |||||||
| chr22:29256678 | A | G | 1 | a0002c0002t0003g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1205-2139A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256678 | |||||||
| chr22:29256782 | A | G | 2 | a0002c0002t0003g0196 a0005c0007t0003g0187 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1205-2035A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256782 | |||||||
| chr22:29256858 | A | T | 1 | a0001c0001t0001g0328 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1205-1959A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256858 | |||||||
| chr22:29256860 | GGT | G | 5 | a0002c0002t0011g0305 a0003c0003t0005g0280 a0003c0003t0005g0281 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1205-1953_1205-195 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 29256860 | ||||||
| chr22:29256975 | C | T | 2 | a0002c0002t0003g0196 a0005c0007t0003g0187 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1205-1842C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256975 | |||||||
| chr22:29257047 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1205-1770G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257047 | |||||||
| chr22:29257066 | A | T | 4 | a0002c0002t0002g0200 a0002c0002t0004g0001 a0002c0002t0004g0028 others(1): Show |
5 | HG02647.hp1 HG02717.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1205-1751A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257066 | |||||||
| chr22:29257139 | C | T | 7 | a0001c0001t0002g0284 a0002c0002t0002g0015 a0002c0002t0002g0275 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1205-1678C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257139 | |||||||
| chr22:29257210 | G | T | 1 | a0001c0001t0003g0113 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1205-1607G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257210 | |||||||
| chr22:29257420 | C | T | 20 | a0001c0001t0003g0002 a0001c0001t0003g0067 a0001c0001t0003g0103 others(17): Show |
22 | HG00558.hp2 HG00609.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.1205-1397C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257420 | |||||||
| chr22:29257421 | G | A | 4 | a0001c0001t0003g0337 a0004c0004t0003g0073 a0004c0004t0003g0084 others(1): Show |
4 | HG00099.hp1 HG00642.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1205-1396G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257421 | |||||||
| chr22:29257495 | G | C | 1 | a0001c0001t0001g0340 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1205-1322G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257495 | |||||||
| chr22:29257511 | C | T | 2 | a0002c0002t0002g0192 a0004c0004t0002g0321 |
2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1205-1306C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257511 | |||||||
| chr22:29257519 | G | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0036 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1205-1298G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257519 | |||||||
| chr22:29257575 | T | C | 332 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(329): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1205-1242T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257575 | |||||||
| chr22:29257622 | G | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
117 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.1205-1195G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257622 | |||||||
| chr22:29257690 | G | A | 2 | a0001c0001t0002g0244 a0002c0002t0002g0250 |
2 | HG02080.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1205-1127G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257690 | |||||||
| chr22:29257717 | C | T | 7 | a0001c0001t0002g0284 a0002c0002t0002g0015 a0002c0002t0002g0275 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1205-1100C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257717 | |||||||
| chr22:29257757 | T | C | 20 | a0001c0001t0003g0002 a0001c0001t0003g0067 a0001c0001t0003g0103 others(17): Show |
22 | HG00558.hp2 HG00609.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.1205-1060T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257757 | |||||||
| chr22:29257766 | C | T | 1 | a0001c0001t0003g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1205-1051C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257766 | |||||||
| chr22:29257852 | T | C | 1 | a0005c0007t0003g0187 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1205-965T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257852 | |||||||
| chr22:29257886 | G | A | 13 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0150 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1205-931G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257886 | |||||||
| chr22:29257924 | C | G | 4 | a0001c0001t0002g0244 a0001c0001t0002g0297 a0001c0001t0002g0306 others(1): Show |
4 | HG02080.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1205-893C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257924 | |||||||
| chr22:29257940 | G | A | 1 | a0002c0002t0003g0314 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1205-877G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257940 | |||||||
| chr22:29257940 | G | T | 83 | a0001c0001t0002g0006 a0001c0001t0002g0053 a0001c0001t0002g0055 others(80): Show |
83 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1205-877G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257940 | |||||||
| chr22:29258015 | C | T | 173 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(170): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1205-802C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29258015 | |||||||
| chr22:29258031 | C | G | 1 | a0002c0002t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1205-786C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29258031 | |||||||
| chr22:29258728 | G | A | 1 | a0001c0001t0003g0309 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1205-89G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29258728 |