Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25896 |
| ensemblid | ENSG00000143493.13 |
| hgncid | 24484 |
| symbol | INTS7 |
| name | integrator complex subunit 7 |
| refseq_nuc | NM_015434.4 |
| refseq_prot | NP_056249.1 |
| ensembl_nuc | ENST00000366994.8 |
| ensembl_prot | ENSP00000355961.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 211940403 |
| end | 212035557 |
| strand | - |
| ver | v1.2 |
| region | chr1:211940403-212035557 |
| region5000 | chr1:211935403-212040557 |
| regionname0 | INTS7_chr1_211940403_212035557 |
| regionname5000 | INTS7_chr1_211935403_212040557 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 962 | 344 | 71 | 62 | 149 | 16 | 44 | 115 | INTS7_chr1_211935403_212040557 | INTS7 | MASNS others(957): Show |
chr1 | 211935403 | 212040557 |
| a0002 | 0/0 | 962 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | MASNS others(957): Show |
chr1 | 211935403 | 212040557 |
| a0003 | 0/0 | 962 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | MASNS others(957): Show |
chr1 | 211935403 | 212040557 |
| a0004 | 0/0 | 962 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | MASNS others(957): Show |
chr1 | 211935403 | 212040557 |
| a0005 | 0/0 | 962 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | MASNS others(957): Show |
chr1 | 211935403 | 212040557 |
| a0006 | 0/0 | 962 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | MASNS others(957): Show |
chr1 | 211935403 | 212040557 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2886 | 328 | 61 | 62 | 144 | 15 | 44 | INTS7_chr1_211935403_212040557 | INTS7 | ATGGC others(2881): Show |
chr1 | 211935403 | 212040557 | ||
| a0001c0002 | 0/0 | 2886 | 8 | 8 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | ATGGC others(2881): Show |
chr1 | 211935403 | 212040557 | ||
| a0001c0004 | 0/0 | 2886 | 3 | 2 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | ATGGC others(2881): Show |
chr1 | 211935403 | 212040557 | ||
| a0001c0005 | 0/0 | 2886 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | ATGGC others(2881): Show |
chr1 | 211935403 | 212040557 | ||
| a0001c0006 | 0/0 | 2886 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | ATGGC others(2881): Show |
chr1 | 211935403 | 212040557 | ||
| a0001c0010 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | ATGGC others(2881): Show |
chr1 | 211935403 | 212040557 | ||
| a0002c0003 | 0/0 | 2886 | 3 | 3 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | ATGGC others(2881): Show |
chr1 | 211935403 | 212040557 | ||
| a0002c0007 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | ATGGC others(2881): Show |
chr1 | 211935403 | 212040557 | ||
| a0003c0008 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | ATGGC others(2881): Show |
chr1 | 211935403 | 212040557 | ||
| a0004c0011 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | ATGGC others(2881): Show |
chr1 | 211935403 | 212040557 | ||
| a0005c0009 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | ATGGC others(2881): Show |
chr1 | 211935403 | 212040557 | ||
| a0006c0012 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | ATGGC others(2881): Show |
chr1 | 211935403 | 212040557 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4430 | 92 | 14 | 12 | 54 | 2 | 9 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0002 | 0/0 | 4430 | 91 | 5 | 18 | 46 | 8 | 14 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0003 | 0/1 | 4430 | 74 | 9 | 16 | 33 | 2 | 13 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0004 | 0/0 | 4430 | 36 | 18 | 3 | 7 | 1 | 7 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0005 | 0/0 | 4430 | 10 | 8 | 2 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0006 | 0/0 | 4430 | 7 | 0 | 7 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0008 | 0/0 | 4430 | 3 | 1 | 2 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0009 | 0/0 | 4430 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0010 | 0/0 | 4430 | 3 | 0 | 0 | 3 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0011 | 0/0 | 4430 | 2 | 2 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0012 | 0/0 | 4430 | 2 | 0 | 0 | 0 | 2 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0013 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0014 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0016 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0017 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0018 | 0/0 | 4430 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0019 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0001t0023 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0002t0005 | 0/0 | 4430 | 5 | 5 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0002t0009 | 0/0 | 4430 | 2 | 2 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0002t0015 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0004t0007 | 0/0 | 4430 | 2 | 2 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0004t0022 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0005t0001 | 0/0 | 4430 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0006t0001 | 0/0 | 4430 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0001c0010t0002 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0002c0003t0007 | 0/0 | 4430 | 2 | 2 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0002c0003t0020 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0002c0007t0021 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0003c0008t0002 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0004c0011t0001 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0005c0009t0001 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| a0006c0012t0001 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | GTAAC others(4425): Show |
chr1 | 211935403 | 212040557 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0005g0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0006g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0006g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0008g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0008g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0009g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0010g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0010g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0010g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0011g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0012g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0012g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0013g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0014g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0016g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0017g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0018g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0019g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0001t0023g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0002t0005g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0002t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0002t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0002t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0002t0015g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0004t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0004t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0004t0022g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0005t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0006t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0006t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0001c0010t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0002c0003t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0002c0003t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0002c0003t0020g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0002c0007t0021g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0003c0008t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0004c0011t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0005c0009t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| a0006c0012t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0012 | EUR | GBR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0217 | EUR | GBR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0178 | EUR | FIN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00323 | hp2 | a0001 | c0004 | t0022 | g0322 | EUR | FIN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0254 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00642 | hp1 | a0001 | c0001 | t0009 | g0198 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0280 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0023 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0252 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0037 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0278 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0123 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0130 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0036 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0259 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0292 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0061 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0041 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0122 | EUR | IBS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01516 | hp1 | a0001 | c0001 | t0012 | g0325 | EUR | IBS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0216 | EUR | IBS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01517 | hp2 | a0001 | c0001 | t0012 | g0324 | EUR | IBS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0155 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01952 | hp2 | a0001 | c0001 | t0018 | g0305 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0306 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02132 | hp2 | a0003 | c0008 | t0002 | g0223 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02135 | hp1 | a0004 | c0011 | t0001 | g0043 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0116 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | CDX | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02257 | hp1 | a0002 | c0003 | t0007 | g0316 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02280 | hp1 | a0001 | c0002 | t0009 | g0033 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0311 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02572 | hp2 | a0001 | c0001 | t0011 | g0202 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02630 | hp2 | a0001 | c0004 | t0007 | g0321 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0315 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0276 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0260 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0134 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0263 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02922 | hp1 | a0001 | c0002 | t0005 | g0003 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02965 | hp1 | a0002 | c0003 | t0020 | g0318 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02965 | hp2 | a0001 | c0001 | t0023 | g0323 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0309 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02976 | hp1 | a0002 | c0003 | t0007 | g0317 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0167 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0135 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03098 | hp2 | a0001 | c0004 | t0007 | g0320 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03225 | hp1 | a0001 | c0002 | t0005 | g0003 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0314 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03453 | hp2 | a0001 | c0001 | t0016 | g0313 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0258 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0166 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0312 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03579 | hp1 | a0001 | c0001 | t0019 | g0203 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0271 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0277 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0063 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03831 | hp2 | a0001 | c0001 | t0013 | g0270 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0262 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0273 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0266 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0104 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18522 | hp1 | a0001 | c0002 | t0005 | g0003 | AFR | YRI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | YRI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | CHB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | CHB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | CHB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18906 | hp1 | a0001 | c0002 | t0015 | g0030 | AFR | YRI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | YRI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18952 | hp1 | a0001 | c0001 | t0014 | g0181 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18979 | hp1 | a0001 | c0001 | t0010 | g0189 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18991 | hp1 | a0001 | c0010 | t0002 | g0250 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18991 | hp2 | a0001 | c0006 | t0001 | g0121 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18994 | hp1 | a0001 | c0001 | t0010 | g0185 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA18998 | hp2 | a0001 | c0005 | t0001 | g0076 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19005 | hp1 | a0001 | c0006 | t0001 | g0102 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0133 | AFR | LWK | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19030 | hp2 | a0001 | c0002 | t0005 | g0028 | AFR | LWK | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0204 | AFR | LWK | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | LWK | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19058 | hp1 | a0001 | c0005 | t0001 | g0097 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19068 | hp2 | a0005 | c0009 | t0001 | g0053 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19084 | hp1 | a0001 | c0001 | t0010 | g0184 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19240 | hp1 | a0001 | c0001 | t0017 | g0025 | AFR | YRI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA19240 | hp2 | a0006 | c0012 | t0001 | g0156 | AFR | YRI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA20129 | hp1 | a0001 | c0002 | t0005 | g0029 | AFR | ASW | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | ASW | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0275 | EUR | TSI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0014 | EUR | TSI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0182 | EUR | TSI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0255 | EUR | TSI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0272 | SAS | GIH | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | GIH | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG02559 | hp2 | a0002 | c0007 | t0021 | g0319 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0035 | AFR | USA | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| HG06807 | hp2 | a0001 | c0002 | t0009 | g0034 | AFR | USA | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | USA | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | USA | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0201 | REF | REF | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0153 | REF | REF | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:211942044 | G | A | 1 | a0004 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.2669C>T | p.Thr890Ile | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 2789/4430 | 2669/2889 | 890/962 | chr1 | 211942044 | |||
| chr1:211967939 | A | G | 1 | a0005 | 1 | NA19068.hp2 | missense_variant | MODERATE | c.2053T>C | p.Tyr685His | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/20 | 2173/4430 | 2053/2889 | 685/962 | chr1 | 211967939 | |||
| chr1:211976665 | T | C | 1 | a0006 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1525A>G | p.Ser509Gly | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/20 | 1645/4430 | 1525/2889 | 509/962 | chr1 | 211976665 | |||
| chr1:211981112 | C | T | 1 | a0003 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.1211G>A | p.Gly404Asp | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/20 | 1331/4430 | 1211/2889 | 404/962 | chr1 | 211981112 | |||
| chr1:211987897 | C | T | 1 | a0002 | 4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.986G>A | p.Ser329Asn | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/20 | 1106/4430 | 986/2889 | 329/962 | chr1 | 211987897 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:211941971 | A | G | 1 | a0001c0005 | 2 | NA18998.hp2 NA19058.hp1 |
synonymous_variant | LOW | c.2742T>C | p.Asn914Asn | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 2862/4430 | 2742/2889 | 914/962 | chr1 | 211941971 | |||
| chr1:211944874 | G | A | 1 | a0001c0002 | 8 | HG02280.hp1 HG02922.hp1 HG03225.hp1 others(5): Show |
synonymous_variant | LOW | c.2511C>T | p.His837His | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/20 | 2631/4430 | 2511/2889 | 837/962 | chr1 | 211944874 | |||
| chr1:211946703 | G | A | 2 | a0001c0004 a0002c0003 |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.2319C>T | p.His773His | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/20 | 2439/4430 | 2319/2889 | 773/962 | chr1 | 211946703 | |||
| chr1:211952653 | A | G | 1 | a0001c0010 | 1 | NA18991.hp1 | synonymous_variant | LOW | c.2232T>C | p.Tyr744Tyr | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/20 | 2352/4430 | 2232/2889 | 744/962 | chr1 | 211952653 | |||
| chr1:211981147 | G | A | 1 | a0001c0006 | 2 | NA18991.hp2 NA19005.hp1 |
synonymous_variant | LOW | c.1176C>T | p.Ser392Ser | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/20 | 1296/4430 | 1176/2889 | 392/962 | chr1 | 211981147 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:211940491 | T | C | 1 | a0001c0001t0017 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1333A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 1333 | chr1 | 211940491 | ||||||
| chr1:211940553 | A | C | 4 | a0001c0001t0005 a0001c0001t0017 a0001c0002t0005 others(1): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1271T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 1271 | chr1 | 211940553 | ||||||
| chr1:211940628 | C | T | 1 | a0001c0004t0022 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1196G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 1196 | chr1 | 211940628 | ||||||
| chr1:211940653 | G | A | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(23): Show |
245 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*1171C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 1171 | chr1 | 211940653 | ||||||
| chr1:211940925 | T | A | 2 | a0001c0001t0011 a0001c0001t0019 |
3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*899A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 899 | chr1 | 211940925 | ||||||
| chr1:211940925 | T | C | 1 | a0001c0001t0018 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*899A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 899 | chr1 | 211940925 | ||||||
| chr1:211940942 | CTT | C | 1 | a0001c0001t0003 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*880_*881delAA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 880 | chr1 | 211940942 | ||||||
| chr1:211941081 | C | T | 1 | a0001c0001t0008 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*743G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 743 | chr1 | 211941081 | ||||||
| chr1:211941083 | G | C | 1 | a0001c0001t0006 | 7 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*741C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 741 | chr1 | 211941083 | ||||||
| chr1:211941150 | G | A | 1 | a0001c0001t0014 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*674C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 674 | chr1 | 211941150 | ||||||
| chr1:211941162 | C | T | 1 | a0001c0001t0016 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 662 | chr1 | 211941162 | ||||||
| chr1:211941169 | A | C | 1 | a0001c0002t0015 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*655T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 655 | chr1 | 211941169 | ||||||
| chr1:211941320 | A | G | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0014 others(2): Show |
97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*504T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 504 | chr1 | 211941320 | ||||||
| chr1:211941321 | G | A | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0014 others(2): Show |
97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*503C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 503 | chr1 | 211941321 | ||||||
| chr1:211941324 | C | G | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0014 others(2): Show |
97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*500G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 500 | chr1 | 211941324 | ||||||
| chr1:211941363 | A | T | 1 | a0001c0001t0011 | 2 | HG02572.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*461T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 461 | chr1 | 211941363 | ||||||
| chr1:211941393 | T | A | 2 | a0001c0001t0009 a0001c0002t0009 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*431A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 431 | chr1 | 211941393 | ||||||
| chr1:211941398 | C | T | 1 | a0001c0001t0013 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*426G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 426 | chr1 | 211941398 | ||||||
| chr1:211941404 | C | T | 2 | a0001c0001t0009 a0001c0002t0009 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*420G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 420 | chr1 | 211941404 | ||||||
| chr1:211941444 | G | A | 1 | a0001c0001t0010 | 3 | NA18979.hp1 NA18994.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*380C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 380 | chr1 | 211941444 | ||||||
| chr1:211941518 | T | C | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(20): Show |
205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*306A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 306 | chr1 | 211941518 | ||||||
| chr1:211941727 | T | G | 4 | a0001c0004t0007 a0001c0004t0022 a0002c0003t0007 others(1): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*97A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 97 | chr1 | 211941727 | ||||||
| chr1:211941745 | C | G | 1 | a0002c0003t0020 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*79G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 79 | chr1 | 211941745 | ||||||
| chr1:212035474 | C | A | 5 | a0001c0004t0007 a0001c0004t0022 a0002c0003t0007 others(2): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-37G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/20 | 37 | chr1 | 212035474 | ||||||
| chr1:212035502 | C | A | 1 | a0001c0001t0023 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-65G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/20 | 65 | chr1 | 212035502 | ||||||
| chr1:212035516 | T | C | 1 | a0001c0001t0012 | 2 | HG01516.hp1 HG01517.hp2 |
5_prime_UTR_variant | MODIFIER | c.-79A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/20 | 79 | chr1 | 212035516 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:211942253 | T | C | 1 | a0002c0007t0021g0319 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2602-142A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942253 | |||||||
| chr1:211942263 | A | G | 3 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 |
3 | HG02257.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2602-152T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942263 | |||||||
| chr1:211942310 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0090 |
2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2602-199G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942310 | |||||||
| chr1:211942329 | C | T | 1 | a0001c0001t0002g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2602-218G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942329 | |||||||
| chr1:211942384 | C | A | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2602-273G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942384 | |||||||
| chr1:211942393 | T | C | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2602-282A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942393 | |||||||
| chr1:211942597 | C | T | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2602-486G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942597 | |||||||
| chr1:211942615 | T | C | 6 | a0001c0001t0009g0198 a0001c0001t0011g0202 a0001c0001t0011g0204 others(3): Show |
6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2602-504A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942615 | |||||||
| chr1:211942670 | C | A | 18 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(15): Show |
18 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2602-559G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942670 | |||||||
| chr1:211942795 | A | T | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2602-684T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942795 | |||||||
| chr1:211942812 | C | G | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2602-701G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942812 | |||||||
| chr1:211942838 | A | T | 1 | a0001c0001t0001g0146 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2602-727T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942838 | |||||||
| chr1:211942891 | G | A | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2602-780C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942891 | |||||||
| chr1:211942949 | T | C | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2602-838A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942949 | |||||||
| chr1:211943082 | A | G | 6 | a0001c0001t0009g0198 a0001c0001t0011g0202 a0001c0001t0011g0204 others(3): Show |
6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2602-971T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943082 | |||||||
| chr1:211943218 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2602-1107T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943218 | |||||||
| chr1:211943242 | G | GT | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2602-1132dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943242 | |||||||
| chr1:211943259 | C | G | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2602-1148G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943259 | |||||||
| chr1:211943260 | G | A | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2602-1149C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943260 | |||||||
| chr1:211943470 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2601+1314G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943470 | |||||||
| chr1:211943517 | T | C | 1 | a0001c0001t0003g0166 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2601+1267A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943517 | |||||||
| chr1:211943627 | G | A | 1 | a0001c0001t0003g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2601+1157C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943627 | |||||||
| chr1:211943723 | T | A | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2601+1061A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943723 | |||||||
| chr1:211943863 | A | C | 21 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0060 others(18): Show |
23 | HG01168.hp1 HG01175.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.2601+921T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943863 | |||||||
| chr1:211944074 | T | C | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2601+710A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944074 | |||||||
| chr1:211944208 | G | A | 1 | a0001c0001t0002g0031 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2601+576C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944208 | |||||||
| chr1:211944276 | G | A | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2601+508C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944276 | |||||||
| chr1:211944307 | G | A | 8 | a0001c0001t0011g0202 a0001c0001t0011g0204 a0001c0004t0007g0320 others(5): Show |
8 | HG00323.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2601+477C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944307 | |||||||
| chr1:211944408 | G | A | 4 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 others(1): Show |
4 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2601+376C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944408 | |||||||
| chr1:211944426 | T | C | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2601+358A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944426 | |||||||
| chr1:211944569 | T | C | 1 | a0001c0001t0003g0168 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2601+215A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944569 | |||||||
| chr1:211944665 | C | T | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2601+119G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944665 | |||||||
| chr1:211944725 | C | T | 1 | a0001c0001t0008g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2601+59G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944725 | |||||||
| chr1:211945024 | A | G | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2416-55T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945024 | |||||||
| chr1:211945083 | C | A | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2416-114G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945083 | |||||||
| chr1:211945089 | C | G | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2416-120G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945089 | |||||||
| chr1:211945155 | A | C | 1 | a0001c0001t0004g0009 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2416-186T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945155 | |||||||
| chr1:211945396 | C | T | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2416-427G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945396 | |||||||
| chr1:211945445 | G | A | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2416-476C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945445 | |||||||
| chr1:211945501 | C | T | 7 | a0001c0001t0002g0015 a0001c0004t0007g0320 a0001c0004t0007g0321 others(4): Show |
8 | HG00323.hp2 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.2416-532G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945501 | |||||||
| chr1:211945518 | C | T | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2416-549G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945518 | |||||||
| chr1:211945579 | T | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0142 |
2 | HG01106.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2416-610A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945579 | |||||||
| chr1:211945598 | C | T | 1 | a0001c0001t0004g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2416-629G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945598 | |||||||
| chr1:211945628 | G | A | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2416-659C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945628 | |||||||
| chr1:211945912 | G | T | 5 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0173 others(2): Show |
5 | NA18948.hp1 NA19002.hp1 NA19067.hp2 others(2): Show |
intron_variant | MODIFIER | c.2415+695C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945912 | |||||||
| chr1:211946035 | G | A | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2415+572C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211946035 | |||||||
| chr1:211946173 | C | T | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2415+434G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211946173 | |||||||
| chr1:211946333 | A | G | 1 | a0001c0004t0022g0322 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2415+274T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211946333 | |||||||
| chr1:211946341 | C | T | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2415+266G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211946341 | |||||||
| chr1:211946354 | A | C | 4 | a0001c0001t0002g0014 a0001c0001t0002g0176 a0001c0001t0002g0182 others(1): Show |
5 | HG01192.hp2 HG01361.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.2415+253T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211946354 | |||||||
| chr1:211946462 | C | T | 44 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0003g0164 others(41): Show |
48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2415+145G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211946462 | |||||||
| chr1:211946955 | CCAAG | C | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2317-254_2317-251d others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211946955 | |||||||
| chr1:211946983 | A | G | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2317-278T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211946983 | |||||||
| chr1:211947135 | T | C | 3 | a0001c0001t0003g0170 a0001c0001t0003g0292 a0001c0001t0003g0293 |
3 | HG01255.hp1 NA19067.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2317-430A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947135 | |||||||
| chr1:211947168 | G | C | 17 | a0001c0001t0003g0094 a0001c0001t0003g0163 a0001c0001t0003g0254 others(14): Show |
17 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.2317-463C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947168 | |||||||
| chr1:211947448 | T | C | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2317-743A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947448 | |||||||
| chr1:211947572 | C | A | 5 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0001t0004g0050 others(2): Show |
5 | HG01884.hp1 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2317-867G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947572 | |||||||
| chr1:211947595 | C | T | 1 | a0002c0003t0020g0318 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2317-890G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947595 | |||||||
| chr1:211947624 | T | C | 2 | a0001c0001t0003g0094 a0001c0001t0003g0261 |
2 | HG02083.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2317-919A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947624 | |||||||
| chr1:211947626 | A | G | 2 | a0001c0001t0001g0160 a0006c0012t0001g0156 |
2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2317-921T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947626 | |||||||
| chr1:211947666 | C | G | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2317-961G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947666 | |||||||
| chr1:211947796 | A | G | 5 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
5 | HG00738.hp2 HG00741.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.2317-1091T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947796 | |||||||
| chr1:211947799 | T | C | 1 | a0001c0010t0002g0250 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2317-1094A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947799 | |||||||
| chr1:211947948 | C | T | 4 | a0001c0002t0005g0003 a0001c0002t0005g0028 a0001c0002t0005g0029 others(1): Show |
6 | HG02922.hp1 HG03225.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.2317-1243G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947948 | |||||||
| chr1:211947999 | T | C | 14 | a0001c0001t0001g0109 a0001c0001t0003g0017 a0001c0001t0003g0200 others(11): Show |
21 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2317-1294A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947999 | |||||||
| chr1:211948068 | T | C | 84 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(81): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.2317-1363A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948068 | |||||||
| chr1:211948157 | T | G | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2317-1452A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948157 | |||||||
| chr1:211948162 | A | AT | 10 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0157 others(7): Show |
12 | HG00323.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2317-1458dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948162 | |||||||
| chr1:211948209 | C | T | 6 | a0001c0001t0009g0198 a0001c0001t0011g0202 a0001c0001t0011g0204 others(3): Show |
6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2317-1504G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948209 | |||||||
| chr1:211948461 | G | A | 1 | a0002c0007t0021g0319 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2317-1756C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948461 | |||||||
| chr1:211948478 | C | T | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2317-1773G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948478 | |||||||
| chr1:211948678 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.2317-1973G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948678 | |||||||
| chr1:211948697 | G | A | 1 | a0001c0004t0007g0321 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2317-1992C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948697 | |||||||
| chr1:211948699 | T | TTTTTG | 3 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 |
3 | HG02257.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2317-1999_2317-199 others(9): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948699 | |||||||
| chr1:211948719 | G | T | 1 | a0001c0001t0003g0266 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2317-2014C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948719 | |||||||
| chr1:211948792 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0110 |
2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2317-2087G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948792 | |||||||
| chr1:211948793 | G | A | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2317-2088C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948793 | |||||||
| chr1:211948803 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.2317-2098C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948803 | |||||||
| chr1:211948943 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2317-2238C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948943 | |||||||
| chr1:211948948 | A | G | 18 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(15): Show |
18 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2317-2243T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948948 | |||||||
| chr1:211949226 | T | C | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2317-2521A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211949226 | |||||||
| chr1:211949484 | T | C | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2317-2779A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211949484 | |||||||
| chr1:211949529 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2317-2824G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211949529 | |||||||
| chr1:211949536 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2317-2831T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211949536 | |||||||
| chr1:211949839 | A | G | 6 | a0001c0001t0009g0198 a0001c0001t0011g0202 a0001c0001t0011g0204 others(3): Show |
6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+2730T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211949839 | |||||||
| chr1:211949879 | T | C | 18 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(15): Show |
18 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2316+2690A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211949879 | |||||||
| chr1:211949962 | T | C | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2316+2607A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211949962 | |||||||
| chr1:211950009 | A | G | 6 | a0001c0001t0009g0198 a0001c0001t0011g0202 a0001c0001t0011g0204 others(3): Show |
6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+2560T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950009 | |||||||
| chr1:211950053 | C | G | 1 | a0001c0001t0002g0268 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2316+2516G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950053 | |||||||
| chr1:211950278 | CTTAT | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0054 others(8): Show |
12 | HG02132.hp1 NA18945.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.2316+2287_2316+229 others(8): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950278 | |||||||
| chr1:211950421 | G | A | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+2148C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950421 | |||||||
| chr1:211950487 | G | GT | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2316+2081dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950487 | |||||||
| chr1:211950598 | C | T | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+1971G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950598 | |||||||
| chr1:211950600 | A | G | 1 | a0002c0007t0021g0319 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2316+1969T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950600 | |||||||
| chr1:211950613 | G | A | 13 | a0001c0001t0003g0017 a0001c0001t0003g0200 a0001c0001t0005g0001 others(10): Show |
20 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2316+1956C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950613 | |||||||
| chr1:211950697 | T | C | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2316+1872A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950697 | |||||||
| chr1:211950777 | C | A | 1 | a0001c0001t0002g0228 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2316+1792G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950777 | |||||||
| chr1:211950782 | C | T | 1 | a0001c0001t0002g0228 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2316+1787G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950782 | |||||||
| chr1:211950943 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2316+1626T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950943 | |||||||
| chr1:211951012 | C | G | 3 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 |
3 | HG02257.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2316+1557G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951012 | |||||||
| chr1:211951170 | G | C | 1 | a0001c0001t0004g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2316+1399C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951170 | |||||||
| chr1:211951201 | G | A | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+1368C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951201 | |||||||
| chr1:211951239 | C | T | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+1330G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951239 | |||||||
| chr1:211951242 | C | T | 9 | a0001c0001t0003g0094 a0001c0001t0003g0163 a0001c0001t0003g0254 others(6): Show |
9 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.2316+1327G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951242 | |||||||
| chr1:211951257 | C | T | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2316+1312G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951257 | |||||||
| chr1:211951316 | G | GT | 29 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0003g0170 others(26): Show |
33 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.2316+1252dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951316 | |||||||
| chr1:211951317 | T | C | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+1252A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951317 | |||||||
| chr1:211951429 | G | T | 18 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(15): Show |
18 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2316+1140C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951429 | |||||||
| chr1:211951508 | A | T | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2316+1061T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951508 | |||||||
| chr1:211951601 | C | T | 75 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(72): Show |
79 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.2316+968G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951601 | |||||||
| chr1:211951714 | C | T | 5 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0001c0001t0002g0244 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2316+855G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951714 | |||||||
| chr1:211951808 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2316+761G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951808 | |||||||
| chr1:211951812 | C | T | 5 | a0001c0001t0004g0045 a0001c0001t0004g0046 a0001c0001t0004g0047 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2316+757G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951812 | |||||||
| chr1:211951813 | G | A | 4 | a0001c0001t0002g0016 a0001c0004t0007g0320 a0001c0004t0007g0321 others(1): Show |
5 | HG00323.hp2 HG00639.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2316+756C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951813 | |||||||
| chr1:211951918 | G | A | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+651C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951918 | |||||||
| chr1:211952064 | CCAA | C | 4 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 others(1): Show |
4 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2316+502_2316+504d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211952064 | |||||||
| chr1:211952088 | T | G | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2316+481A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211952088 | |||||||
| chr1:211952115 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2316+454A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211952115 | |||||||
| chr1:211952151 | C | T | 1 | a0001c0001t0003g0272 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2316+418G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211952151 | |||||||
| chr1:211952444 | C | T | 1 | a0001c0001t0003g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2316+125G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211952444 | |||||||
| chr1:211952468 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2316+101G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211952468 | |||||||
| chr1:211952485 | G | C | 5 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0001t0004g0050 others(2): Show |
5 | HG01884.hp1 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2316+84C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211952485 | |||||||
| chr1:211952712 | G | A | 4 | a0001c0001t0004g0103 a0001c0001t0004g0111 a0001c0001t0004g0137 others(1): Show |
4 | NA18990.hp2 NA19012.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.2184-11C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211952712 | |||||||
| chr1:211952828 | G | T | 1 | a0001c0001t0003g0309 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2184-127C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211952828 | |||||||
| chr1:211952858 | T | C | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2184-157A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211952858 | |||||||
| chr1:211953236 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2184-535C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953236 | |||||||
| chr1:211953298 | T | A | 1 | a0001c0001t0002g0212 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2184-597A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953298 | |||||||
| chr1:211953392 | T | C | 2 | a0001c0001t0008g0035 a0001c0001t0008g0036 |
2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2184-691A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953392 | |||||||
| chr1:211953404 | TTTA | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0100 a0004c0011t0001g0043 |
3 | HG02129.hp2 HG02135.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.2184-706_2184-704d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953404 | |||||||
| chr1:211953441 | G | A | 1 | a0002c0007t0021g0319 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2184-740C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953441 | |||||||
| chr1:211953447 | T | C | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2184-746A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953447 | |||||||
| chr1:211953524 | A | G | 2 | a0001c0001t0002g0013 a0001c0001t0002g0175 |
3 | HG00642.hp2 HG01257.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.2184-823T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953524 | |||||||
| chr1:211953655 | G | T | 1 | a0001c0001t0008g0037 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2184-954C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953655 | |||||||
| chr1:211953669 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2184-968G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953669 | |||||||
| chr1:211953863 | A | G | 5 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0001c0001t0002g0244 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2184-1162T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953863 | |||||||
| chr1:211953974 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2184-1273G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953974 | |||||||
| chr1:211954085 | T | C | 6 | a0001c0001t0009g0198 a0001c0001t0011g0202 a0001c0001t0011g0204 others(3): Show |
6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-1384A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954085 | |||||||
| chr1:211954092 | C | T | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-1391G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954092 | |||||||
| chr1:211954111 | A | T | 89 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(86): Show |
97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2184-1410T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954111 | |||||||
| chr1:211954226 | C | T | 3 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0037 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2184-1525G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954226 | |||||||
| chr1:211954227 | G | A | 50 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0031 others(47): Show |
52 | HG00140.hp2 HG00597.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.2184-1526C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954227 | |||||||
| chr1:211954320 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2184-1619G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954320 | |||||||
| chr1:211954416 | G | C | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-1715C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954416 | |||||||
| chr1:211954431 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2184-1730A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954431 | |||||||
| chr1:211954466 | T | C | 2 | a0001c0006t0001g0102 a0001c0006t0001g0121 |
2 | NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2184-1765A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954466 | |||||||
| chr1:211954539 | G | T | 13 | a0001c0001t0003g0017 a0001c0001t0003g0200 a0001c0001t0005g0001 others(10): Show |
20 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2184-1838C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954539 | |||||||
| chr1:211954678 | G | C | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-1977C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954678 | |||||||
| chr1:211954715 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0079 a0001c0001t0001g0113 others(1): Show |
4 | HG02559.hp2 NA18993.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.2184-2014C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954715 | |||||||
| chr1:211954839 | C | T | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2184-2138G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954839 | |||||||
| chr1:211955046 | A | G | 1 | a0001c0001t0003g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2184-2345T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955046 | |||||||
| chr1:211955072 | G | A | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2184-2371C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955072 | |||||||
| chr1:211955084 | A | G | 1 | a0001c0001t0004g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2184-2383T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955084 | |||||||
| chr1:211955124 | G | T | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2184-2423C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955124 | |||||||
| chr1:211955320 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2184-2619T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955320 | |||||||
| chr1:211955442 | T | C | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2184-2741A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955442 | |||||||
| chr1:211955486 | G | A | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2184-2785C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955486 | |||||||
| chr1:211955634 | G | T | 2 | a0001c0001t0003g0094 a0001c0001t0003g0261 |
2 | HG02083.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2184-2933C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955634 | |||||||
| chr1:211955643 | G | A | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-2942C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955643 | |||||||
| chr1:211955747 | A | T | 17 | a0001c0001t0003g0094 a0001c0001t0003g0163 a0001c0001t0003g0254 others(14): Show |
17 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.2184-3046T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955747 | |||||||
| chr1:211956079 | C | CT | 3 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 |
3 | HG02257.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2184-3379dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211956079 | |||||||
| chr1:211956129 | T | G | 95 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(92): Show |
103 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.2184-3428A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211956129 | |||||||
| chr1:211956176 | A | G | 44 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0003g0164 others(41): Show |
48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2184-3475T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211956176 | |||||||
| chr1:211956228 | G | A | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2184-3527C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211956228 | |||||||
| chr1:211956400 | T | C | 1 | a0001c0001t0002g0267 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2184-3699A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211956400 | |||||||
| chr1:211956808 | A | G | 89 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(86): Show |
97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2184-4107T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211956808 | |||||||
| chr1:211957028 | G | A | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2184-4327C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957028 | |||||||
| chr1:211957092 | C | T | 9 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 others(6): Show |
9 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2184-4391G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957092 | |||||||
| chr1:211957266 | C | T | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2184-4565G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957266 | |||||||
| chr1:211957300 | CT | C | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2184-4600delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957300 | |||||||
| chr1:211957335 | C | T | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-4634G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957335 | |||||||
| chr1:211957477 | T | C | 12 | a0001c0001t0009g0198 a0001c0001t0011g0202 a0001c0001t0011g0204 others(9): Show |
12 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2184-4776A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957477 | |||||||
| chr1:211957495 | G | A | 1 | a0001c0004t0022g0322 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2184-4794C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957495 | |||||||
| chr1:211957530 | A | C | 1 | a0001c0001t0003g0282 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2184-4829T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957530 | |||||||
| chr1:211957531 | G | C | 140 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(137): Show |
152 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.2184-4830C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957531 | |||||||
| chr1:211957537 | A | G | 186 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(183): Show |
205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.2184-4836T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957537 | |||||||
| chr1:211957787 | A | G | 1 | a0001c0001t0004g0047 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2184-5086T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957787 | |||||||
| chr1:211957831 | T | C | 2 | a0001c0001t0005g0022 a0001c0001t0005g0023 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2184-5130A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957831 | |||||||
| chr1:211957933 | T | G | 3 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 |
3 | HG02257.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2184-5232A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957933 | |||||||
| chr1:211958047 | C | T | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2184-5346G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958047 | |||||||
| chr1:211958070 | TA | T | 173 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(170): Show |
192 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.2184-5370delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958070 | |||||||
| chr1:211958071 | A | T | 2 | a0002c0003t0007g0316 a0002c0003t0007g0317 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2184-5370T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958071 | |||||||
| chr1:211958080 | AAC | A | 7 | a0001c0001t0002g0177 a0001c0004t0007g0320 a0001c0004t0007g0321 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2184-5381_2184-538 others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958080 | |||||||
| chr1:211958082 | C | A | 4 | a0001c0001t0009g0198 a0001c0001t0011g0202 a0001c0001t0011g0204 others(1): Show |
4 | HG00642.hp1 HG02572.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2184-5381G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958082 | |||||||
| chr1:211958083 | A | C | 1 | a0001c0001t0002g0177 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2184-5382T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958083 | |||||||
| chr1:211958237 | C | T | 186 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(183): Show |
205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.2184-5536G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958237 | |||||||
| chr1:211958324 | G | A | 3 | a0001c0001t0003g0278 a0001c0001t0003g0279 a0001c0001t0003g0280 |
3 | HG00738.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2184-5623C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958324 | |||||||
| chr1:211958369 | C | A | 1 | a0001c0001t0004g0009 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2184-5668G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958369 | |||||||
| chr1:211958378 | T | A | 13 | a0001c0001t0003g0017 a0001c0001t0003g0200 a0001c0001t0005g0001 others(10): Show |
20 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2184-5677A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958378 | |||||||
| chr1:211958430 | CTTCT | C | 49 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0001c0001t0002g0244 others(46): Show |
53 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.2184-5733_2184-573 others(8): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958430 | |||||||
| chr1:211958449 | T | A | 1 | a0001c0001t0004g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2184-5748A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958449 | |||||||
| chr1:211958486 | C | T | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-5785G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958486 | |||||||
| chr1:211958508 | TTA | T | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-5809_2184-580 others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958508 | |||||||
| chr1:211958563 | T | A | 1 | a0001c0001t0003g0168 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2184-5862A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958563 | |||||||
| chr1:211958610 | C | T | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-5909G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958610 | |||||||
| chr1:211959661 | T | C | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2183+6769A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211959661 | |||||||
| chr1:211959688 | TG | T | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2183+6741delC | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211959688 | |||||||
| chr1:211959860 | C | A | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+6570G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211959860 | |||||||
| chr1:211959876 | C | T | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2183+6554G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211959876 | |||||||
| chr1:211959943 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2183+6487G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211959943 | |||||||
| chr1:211959962 | TC | T | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2183+6467delG | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211959962 | |||||||
| chr1:211960309 | G | T | 3 | a0001c0001t0011g0202 a0001c0001t0011g0204 a0001c0001t0019g0203 |
3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2183+6121C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960309 | |||||||
| chr1:211960333 | A | C | 4 | a0001c0001t0003g0309 a0001c0001t0003g0310 a0001c0001t0003g0311 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183+6097T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960333 | |||||||
| chr1:211960417 | A | T | 1 | a0001c0001t0001g0095 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2183+6013T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960417 | |||||||
| chr1:211960554 | A | C | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2183+5876T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960554 | |||||||
| chr1:211960568 | T | C | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+5862A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960568 | |||||||
| chr1:211960711 | G | A | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2183+5719C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960711 | |||||||
| chr1:211960770 | T | A | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2183+5660A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960770 | |||||||
| chr1:211960990 | A | G | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+5440T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960990 | |||||||
| chr1:211961068 | C | T | 2 | a0001c0001t0002g0213 a0001c0001t0002g0233 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2183+5362G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961068 | |||||||
| chr1:211961146 | A | C | 1 | a0001c0001t0004g0105 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2183+5284T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961146 | |||||||
| chr1:211961263 | C | T | 1 | a0001c0001t0003g0309 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2183+5167G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961263 | |||||||
| chr1:211961345 | A | G | 1 | a0002c0007t0021g0319 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2183+5085T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961345 | |||||||
| chr1:211961430 | C | CT | 7 | a0001c0001t0002g0251 a0001c0004t0007g0320 a0001c0004t0007g0321 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2183+4999dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961430 | |||||||
| chr1:211961523 | G | A | 3 | a0001c0001t0002g0012 a0001c0001t0002g0188 a0001c0001t0002g0195 |
4 | HG00099.hp2 HG01258.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183+4907C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961523 | |||||||
| chr1:211961560 | A | C | 13 | a0001c0001t0003g0017 a0001c0001t0003g0200 a0001c0001t0005g0001 others(10): Show |
20 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2183+4870T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961560 | |||||||
| chr1:211961591 | G | A | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2183+4839C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961591 | |||||||
| chr1:211961617 | C | T | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2183+4813G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961617 | |||||||
| chr1:211961774 | C | T | 3 | a0001c0001t0002g0012 a0001c0001t0002g0188 a0001c0001t0002g0195 |
4 | HG00099.hp2 HG01258.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183+4656G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961774 | |||||||
| chr1:211961793 | G | A | 186 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(183): Show |
205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.2183+4637C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961793 | |||||||
| chr1:211961930 | A | T | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+4500T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961930 | |||||||
| chr1:211961931 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2183+4499T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961931 | |||||||
| chr1:211962199 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2183+4231A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962199 | |||||||
| chr1:211962260 | TA | T | 157 | a0001c0001t0001g0059 a0001c0001t0001g0073 a0001c0001t0001g0144 others(154): Show |
175 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.2183+4169delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962260 | |||||||
| chr1:211962260 | TAA | T | 21 | a0001c0001t0002g0177 a0001c0001t0002g0191 a0001c0001t0002g0205 others(18): Show |
22 | HG00642.hp1 HG01069.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.2183+4168_2183+416 others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962260 | |||||||
| chr1:211962376 | T | G | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+4054A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962376 | |||||||
| chr1:211962561 | A | G | 1 | a0001c0001t0004g0063 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2183+3869T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962561 | |||||||
| chr1:211962611 | A | C | 1 | a0001c0001t0002g0226 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2183+3819T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962611 | |||||||
| chr1:211962686 | C | A | 1 | a0001c0001t0003g0258 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2183+3744G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962686 | |||||||
| chr1:211962728 | T | C | 2 | a0001c0001t0002g0013 a0001c0001t0002g0175 |
3 | HG00642.hp2 HG01257.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.2183+3702A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962728 | |||||||
| chr1:211962762 | G | A | 4 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 others(1): Show |
4 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2183+3668C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962762 | |||||||
| chr1:211962874 | G | A | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2183+3556C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962874 | |||||||
| chr1:211962898 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2183+3532G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962898 | |||||||
| chr1:211962899 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2183+3531A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962899 | |||||||
| chr1:211962900 | A | G | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2183+3530T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962900 | |||||||
| chr1:211962971 | T | C | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+3459A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962971 | |||||||
| chr1:211963089 | A | G | 1 | a0001c0001t0002g0177 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2183+3341T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963089 | |||||||
| chr1:211963100 | G | A | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+3330C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963100 | |||||||
| chr1:211963438 | C | T | 3 | a0001c0001t0011g0202 a0001c0001t0011g0204 a0001c0001t0019g0203 |
3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2183+2992G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963438 | |||||||
| chr1:211963629 | T | C | 6 | a0001c0001t0009g0198 a0001c0001t0011g0202 a0001c0001t0011g0204 others(3): Show |
6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+2801A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963629 | |||||||
| chr1:211963699 | T | C | 44 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0003g0164 others(41): Show |
48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2183+2731A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963699 | |||||||
| chr1:211963754 | A | C | 6 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(3): Show |
6 | HG02622.hp1 HG02886.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+2676T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963754 | |||||||
| chr1:211963774 | A | G | 2 | a0002c0003t0007g0316 a0002c0003t0007g0317 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2183+2656T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963774 | |||||||
| chr1:211963790 | C | A | 1 | a0001c0001t0002g0177 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2183+2640G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963790 | |||||||
| chr1:211963791 | A | C | 1 | a0001c0001t0002g0177 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2183+2639T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963791 | |||||||
| chr1:211963808 | ACT | A | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+2620_2183+262 others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963808 | |||||||
| chr1:211964063 | G | A | 6 | a0001c0001t0004g0008 a0001c0001t0004g0060 a0001c0001t0004g0105 others(3): Show |
7 | HG02258.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2183+2367C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211964063 | |||||||
| chr1:211964263 | C | A | 15 | a0001c0001t0004g0009 a0001c0001t0004g0063 a0001c0001t0004g0103 others(12): Show |
16 | HG01168.hp1 HG01175.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.2183+2167G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211964263 | |||||||
| chr1:211964275 | C | T | 1 | a0001c0001t0004g0050 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2183+2155G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211964275 | |||||||
| chr1:211964440 | C | T | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+1990G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211964440 | |||||||
| chr1:211964632 | A | G | 89 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(86): Show |
97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2183+1798T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211964632 | |||||||
| chr1:211964683 | C | G | 1 | a0001c0001t0002g0240 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2183+1747G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211964683 | |||||||
| chr1:211965185 | TA | T | 22 | a0001c0001t0001g0081 a0001c0001t0003g0094 a0001c0001t0003g0163 others(19): Show |
22 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.2183+1244delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965185 | |||||||
| chr1:211965214 | C | T | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2183+1216G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965214 | |||||||
| chr1:211965302 | A | T | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+1128T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965302 | |||||||
| chr1:211965312 | G | A | 1 | a0001c0001t0004g0124 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2183+1118C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965312 | |||||||
| chr1:211965314 | T | TGCAGAGA others(5): Show |
1 | a0001c0001t0004g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2183+1104_2183+111 others(16): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965314 | |||||||
| chr1:211965348 | G | A | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2183+1082C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965348 | |||||||
| chr1:211965373 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA19057.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.2183+1057C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965373 | |||||||
| chr1:211965434 | A | T | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2183+996T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965434 | |||||||
| chr1:211965499 | T | C | 1 | a0001c0001t0002g0220 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2183+931A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965499 | |||||||
| chr1:211965553 | C | A | 1 | a0001c0001t0002g0013 | 2 | HG01257.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.2183+877G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965553 | |||||||
| chr1:211965577 | G | T | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+853C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965577 | |||||||
| chr1:211965610 | C | T | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(3): Show |
6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+820G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965610 | |||||||
| chr1:211965622 | AAAG | A | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2183+805_2183+807d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965622 | |||||||
| chr1:211965888 | G | A | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2183+542C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965888 | |||||||
| chr1:211966027 | T | C | 1 | a0001c0001t0002g0281 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2183+403A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211966027 | |||||||
| chr1:211966259 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.2183+171C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211966259 | |||||||
| chr1:211966291 | C | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA19057.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.2183+139G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211966291 | |||||||
| chr1:211966504 | T | C | 1 | a0001c0001t0003g0297 | 1 | NA18939.hp1 | splice_region_variant&intron_variant | LOW | c.2115-6A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966504 | |||||||
| chr1:211966529 | T | C | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2115-31A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966529 | |||||||
| chr1:211966554 | C | T | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2115-56G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966554 | |||||||
| chr1:211966714 | C | T | 1 | a0001c0004t0007g0321 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2115-216G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966714 | |||||||
| chr1:211966750 | T | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2115-252A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966750 | |||||||
| chr1:211966757 | C | T | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2115-259G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966757 | |||||||
| chr1:211966871 | T | A | 3 | a0001c0001t0002g0241 a0001c0005t0001g0076 a0001c0005t0001g0097 |
3 | HG01981.hp2 NA18998.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2115-373A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966871 | |||||||
| chr1:211966996 | A | T | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2115-498T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966996 | |||||||
| chr1:211967175 | C | T | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2115-677G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967175 | |||||||
| chr1:211967280 | G | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2114+598C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967280 | |||||||
| chr1:211967451 | C | CA | 134 | a0001c0001t0001g0092 a0001c0001t0001g0108 a0001c0001t0001g0160 others(131): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.2114+426dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967451 | |||||||
| chr1:211967451 | C | CAA | 6 | a0001c0001t0002g0019 a0001c0001t0002g0177 a0001c0001t0002g0229 others(3): Show |
7 | HG02027.hp1 NA18944.hp1 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.2114+425_2114+426d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967451 | |||||||
| chr1:211967451 | CA | C | 35 | a0001c0001t0001g0064 a0001c0001t0001g0077 a0001c0001t0003g0017 others(32): Show |
40 | HG00323.hp2 HG01069.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.2114+426delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967451 | |||||||
| chr1:211967499 | C | G | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2114+379G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967499 | |||||||
| chr1:211967543 | A | T | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2114+335T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967543 | |||||||
| chr1:211967616 | T | C | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2114+262A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967616 | |||||||
| chr1:211967672 | C | T | 1 | a0001c0001t0002g0267 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2114+206G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967672 | |||||||
| chr1:211967756 | CTATA | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0157 others(5): Show |
10 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2114+118_2114+121d others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967756 | |||||||
| chr1:211968027 | T | C | 4 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 others(1): Show |
4 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2011-46A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968027 | |||||||
| chr1:211968035 | C | A | 1 | a0001c0001t0002g0212 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2011-54G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968035 | |||||||
| chr1:211968083 | C | A | 27 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0003g0170 others(24): Show |
31 | HG00423.hp2 HG00733.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.2011-102G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968083 | |||||||
| chr1:211968151 | A | C | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2011-170T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968151 | |||||||
| chr1:211968188 | TTA | T | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2011-209_2011-208d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968188 | |||||||
| chr1:211968330 | A | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2010+183T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968330 | |||||||
| chr1:211968416 | A | T | 1 | a0001c0001t0003g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2010+97T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968416 | |||||||
| chr1:211968418 | T | A | 1 | a0001c0001t0003g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2010+95A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968418 | |||||||
| chr1:211968431 | T | C | 1 | a0001c0001t0003g0166 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2010+82A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968431 | |||||||
| chr1:211968712 | GA | G | 152 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(149): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
splice_region_variant&intron_variant | LOW | c.1816-6delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211968712 | |||||||
| chr1:211968713 | A | G | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1816-6T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211968713 | |||||||
| chr1:211968793 | G | C | 4 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1816-86C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211968793 | |||||||
| chr1:211968897 | T | C | 1 | a0001c0001t0002g0230 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1816-190A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211968897 | |||||||
| chr1:211969199 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1816-492C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969199 | |||||||
| chr1:211969234 | G | A | 4 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 others(1): Show |
4 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1816-527C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969234 | |||||||
| chr1:211969282 | C | CA | 14 | a0001c0001t0002g0209 a0001c0001t0002g0230 a0001c0001t0002g0238 others(11): Show |
14 | HG00323.hp2 HG00597.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1816-576dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969282 | |||||||
| chr1:211969293 | A | C | 7 | a0001c0001t0002g0011 a0001c0001t0002g0174 a0001c0001t0002g0177 others(4): Show |
8 | HG00558.hp2 HG02056.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.1816-586T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969293 | |||||||
| chr1:211969298 | G | A | 169 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(166): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1816-591C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969298 | |||||||
| chr1:211969317 | A | G | 16 | a0001c0001t0003g0017 a0001c0001t0003g0200 a0001c0001t0005g0001 others(13): Show |
23 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1816-610T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969317 | |||||||
| chr1:211969390 | C | T | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1816-683G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969390 | |||||||
| chr1:211969488 | T | A | 1 | a0001c0001t0004g0124 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1816-781A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969488 | |||||||
| chr1:211969489 | G | T | 50 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0031 others(47): Show |
52 | HG00140.hp2 HG00597.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.1816-782C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969489 | |||||||
| chr1:211969551 | C | CT | 13 | a0001c0001t0001g0066 a0001c0001t0001g0080 a0001c0001t0001g0098 others(10): Show |
13 | HG00597.hp1 HG00741.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1816-845dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969551 | |||||||
| chr1:211969551 | CT | C | 149 | a0001c0001t0001g0064 a0001c0001t0001g0138 a0001c0001t0001g0139 others(146): Show |
161 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1816-845delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969551 | |||||||
| chr1:211969551 | CTT | C | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1816-846_1816-845d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969551 | |||||||
| chr1:211969616 | T | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1816-909A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969616 | |||||||
| chr1:211969632 | T | C | 2 | a0001c0001t0003g0301 a0001c0001t0003g0304 |
2 | NA18966.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1816-925A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969632 | |||||||
| chr1:211969657 | A | T | 1 | a0001c0001t0002g0171 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1816-950T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969657 | |||||||
| chr1:211969716 | T | C | 22 | a0001c0001t0003g0021 a0001c0001t0003g0197 a0001c0001t0003g0252 others(19): Show |
22 | HG00323.hp2 HG00642.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1816-1009A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969716 | |||||||
| chr1:211969717 | G | A | 45 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0003g0164 others(42): Show |
49 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1816-1010C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969717 | |||||||
| chr1:211969722 | A | AT | 98 | a0001c0001t0001g0100 a0001c0001t0002g0011 a0001c0001t0002g0012 others(95): Show |
106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1816-1016dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969722 | |||||||
| chr1:211969791 | TCACTG | T | 6 | a0001c0001t0006g0005 a0001c0001t0006g0041 a0001c0001t0006g0061 others(3): Show |
7 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1816-1089_1816-108 others(9): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969791 | |||||||
| chr1:211969864 | G | A | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1816-1157C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969864 | |||||||
| chr1:211969906 | G | T | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1816-1199C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969906 | |||||||
| chr1:211969945 | C | T | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1816-1238G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969945 | |||||||
| chr1:211969959 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1816-1252G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969959 | |||||||
| chr1:211970085 | T | C | 4 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1816-1378A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970085 | |||||||
| chr1:211970231 | C | T | 1 | a0001c0001t0003g0256 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1816-1524G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970231 | |||||||
| chr1:211970255 | G | C | 1 | a0001c0001t0002g0238 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1816-1548C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970255 | |||||||
| chr1:211970576 | G | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1816-1869C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970576 | |||||||
| chr1:211970584 | A | G | 1 | a0001c0001t0003g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1816-1877T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970584 | |||||||
| chr1:211970590 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1816-1883G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970590 | |||||||
| chr1:211970700 | A | C | 1 | a0001c0001t0003g0262 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1816-1993T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970700 | |||||||
| chr1:211970798 | C | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1816-2091G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970798 | |||||||
| chr1:211970909 | G | A | 44 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0003g0164 others(41): Show |
48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1816-2202C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970909 | |||||||
| chr1:211971013 | A | T | 4 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(1): Show |
4 | HG02080.hp2 NA18612.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1816-2306T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971013 | |||||||
| chr1:211971199 | G | GT | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1816-2493dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971199 | |||||||
| chr1:211971200 | T | C | 6 | a0001c0001t0009g0198 a0001c0001t0011g0202 a0001c0001t0011g0204 others(3): Show |
6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1816-2493A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971200 | |||||||
| chr1:211971212 | A | G | 1 | a0001c0001t0003g0293 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1816-2505T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971212 | |||||||
| chr1:211971359 | G | A | 30 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0003g0170 others(27): Show |
34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1816-2652C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971359 | |||||||
| chr1:211971463 | T | C | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1816-2756A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971463 | |||||||
| chr1:211971496 | A | C | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1816-2789T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971496 | |||||||
| chr1:211971639 | G | A | 1 | a0001c0001t0003g0293 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1816-2932C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971639 | |||||||
| chr1:211971659 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1816-2952A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971659 | |||||||
| chr1:211971678 | G | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1816-2971C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971678 | |||||||
| chr1:211971884 | C | A | 84 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(81): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1816-3177G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971884 | |||||||
| chr1:211971910 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1816-3203T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971910 | |||||||
| chr1:211971915 | C | CA | 11 | a0001c0001t0001g0056 a0001c0001t0001g0090 a0001c0001t0001g0096 others(8): Show |
11 | HG01884.hp1 HG02723.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.1816-3209dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971915 | |||||||
| chr1:211971915 | CA | C | 25 | a0001c0001t0001g0074 a0001c0001t0001g0144 a0001c0001t0002g0242 others(22): Show |
25 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1816-3209delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971915 | |||||||
| chr1:211971915 | CAA | C | 106 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0002g0011 others(103): Show |
121 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1816-3210_1816-320 others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971915 | |||||||
| chr1:211971915 | CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1816-3222_1816-320 others(18): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971915 | |||||||
| chr1:211971920 | AAAAAAAA others(10): Show |
A | 2 | a0002c0003t0020g0318 a0002c0007t0021g0319 |
2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1815+3229_1816-321 others(21): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971920 | |||||||
| chr1:211971932 | A | G | 2 | a0001c0001t0004g0009 a0001c0001t0013g0270 |
3 | HG03490.hp2 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1816-3225T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971932 | |||||||
| chr1:211972079 | C | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815+3087G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211972079 | |||||||
| chr1:211972130 | A | G | 1 | a0001c0001t0003g0300 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1815+3036T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211972130 | |||||||
| chr1:211972235 | C | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815+2931G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211972235 | |||||||
| chr1:211972418 | G | A | 1 | a0001c0001t0003g0264 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1815+2748C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211972418 | |||||||
| chr1:211972594 | T | C | 4 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1815+2572A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211972594 | |||||||
| chr1:211972722 | T | C | 5 | a0001c0001t0011g0202 a0001c0001t0011g0204 a0001c0001t0019g0203 others(2): Show |
5 | HG02280.hp1 HG02572.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1815+2444A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211972722 | |||||||
| chr1:211972907 | C | A | 1 | a0001c0001t0002g0269 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1815+2259G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211972907 | |||||||
| chr1:211973076 | G | C | 1 | a0001c0001t0004g0063 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1815+2090C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973076 | |||||||
| chr1:211973224 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1815+1942C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973224 | |||||||
| chr1:211973224 | G | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815+1942C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973224 | |||||||
| chr1:211973372 | A | C | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1815+1794T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973372 | |||||||
| chr1:211973409 | G | T | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1815+1757C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973409 | |||||||
| chr1:211973412 | T | C | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1815+1754A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973412 | |||||||
| chr1:211973483 | T | A | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1815+1683A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973483 | |||||||
| chr1:211973497 | A | T | 44 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0003g0164 others(41): Show |
48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1815+1669T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973497 | |||||||
| chr1:211973541 | C | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815+1625G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973541 | |||||||
| chr1:211973766 | G | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815+1400C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973766 | |||||||
| chr1:211974033 | C | G | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1815+1133G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974033 | |||||||
| chr1:211974241 | A | C | 1 | a0001c0001t0010g0184 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1815+925T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974241 | |||||||
| chr1:211974267 | GAA | G | 27 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0064 others(24): Show |
28 | HG00642.hp1 HG02129.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.1815+897_1815+898d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974267 | |||||||
| chr1:211974267 | GAAAA | G | 33 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0003g0164 others(30): Show |
38 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1815+895_1815+898d others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974267 | |||||||
| chr1:211974267 | GAAAAAA | G | 7 | a0001c0001t0002g0268 a0001c0001t0003g0255 a0001c0001t0003g0258 others(4): Show |
7 | HG02257.hp2 HG03490.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.1815+893_1815+898d others(8): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974267 | |||||||
| chr1:211974268 | AAAAAAAA others(3): Show |
A | 1 | a0001c0002t0009g0033 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1815+888_1815+897d others(12): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974268 | |||||||
| chr1:211974268 | AAAAAAAA others(9): Show |
A | 2 | a0002c0003t0020g0318 a0002c0007t0021g0319 |
2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1815+882_1815+897d others(18): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974268 | |||||||
| chr1:211974268 | AAAAAAAA others(11): Show |
A | 5 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(2): Show |
5 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1815+880_1815+897d others(20): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974268 | |||||||
| chr1:211974270 | A | AAT | 8 | a0001c0001t0002g0178 a0001c0001t0002g0193 a0001c0001t0002g0195 others(5): Show |
8 | HG00323.hp1 HG00733.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1815+895_1815+896i others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | A | AATAT | 8 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(5): Show |
8 | HG00099.hp2 HG01192.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1815+895_1815+896i others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | A | AATATAT | 12 | a0001c0001t0002g0014 a0001c0001t0002g0016 a0001c0001t0002g0175 others(9): Show |
12 | HG00639.hp1 HG00642.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1815+895_1815+896i others(8): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | A | AATATATA others(1): Show |
8 | a0001c0001t0002g0171 a0001c0001t0002g0173 a0001c0001t0002g0174 others(5): Show |
8 | HG01258.hp1 HG03139.hp2 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1815+895_1815+896i others(10): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | A | AATATATA others(3): Show |
10 | a0001c0001t0001g0078 a0001c0001t0002g0179 a0001c0001t0002g0180 others(7): Show |
10 | HG00741.hp1 HG02027.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1815+895_1815+896i others(12): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | A | AATATATA others(5): Show |
7 | a0001c0001t0002g0015 a0001c0001t0003g0167 a0001c0001t0004g0103 others(4): Show |
8 | HG01168.hp1 HG01515.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1815+895_1815+896i others(14): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | A | AATATATA others(7): Show |
1 | a0001c0001t0004g0315 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1815+895_1815+896i others(16): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | A | AATATATA others(9): Show |
4 | a0001c0001t0004g0104 a0001c0001t0004g0137 a0001c0001t0008g0036 others(1): Show |
4 | HG01243.hp1 HG04228.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1815+895_1815+896i others(18): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | A | AATATATA others(11): Show |
2 | a0001c0001t0004g0135 a0001c0001t0008g0035 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1815+895_1815+896i others(20): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | A | AATATATA others(19): Show |
1 | a0001c0001t0004g0149 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1815+895_1815+896i others(28): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | A | T | 2 | a0001c0002t0009g0034 a0004c0011t0001g0043 |
2 | HG02135.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1815+896T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | AAAAAAAA others(1): Show |
A | 18 | a0001c0001t0003g0021 a0001c0001t0003g0094 a0001c0001t0003g0163 others(15): Show |
18 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1815+888_1815+895d others(10): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0003g0309 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1815+886_1815+895d others(12): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1815+884_1815+895d others(14): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1815+882_1815+895d others(16): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | AAAAAAAA others(11): Show |
A | 4 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1815+878_1815+895d others(20): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | AAAAAAAA others(13): Show |
A | 14 | a0001c0001t0003g0017 a0001c0001t0003g0200 a0001c0001t0004g0009 others(11): Show |
22 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1815+876_1815+895d others(22): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974270 | AAAAAAAA others(15): Show |
A | 50 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0031 others(47): Show |
52 | HG00140.hp2 HG00597.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.1815+874_1815+895d others(24): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | |||||||
| chr1:211974272 | A | AAT | 14 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0032 others(11): Show |
17 | HG01071.hp2 HG02004.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.1815+893_1815+894i others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974272 | |||||||
| chr1:211974272 | A | AATATATA others(5): Show |
1 | a0001c0001t0001g0077 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1815+893_1815+894i others(14): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974272 | |||||||
| chr1:211974272 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0161 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1815+893_1815+894i others(16): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974272 | |||||||
| chr1:211974272 | A | T | 77 | a0001c0001t0001g0059 a0001c0001t0001g0078 a0001c0001t0001g0136 others(74): Show |
83 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.1815+894T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974272 | |||||||
| chr1:211974272 | AAAAAATA others(3): Show |
A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA19057.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1815+884_1815+893d others(12): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974272 | |||||||
| chr1:211974274 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0159 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1815+891_1815+892i others(12): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974274 | |||||||
| chr1:211974274 | A | T | 148 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(145): Show |
159 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1815+892T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974274 | |||||||
| chr1:211974276 | A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0090 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1815+889_1815+890i others(14): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974276 | |||||||
| chr1:211974276 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0157 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1815+880_1815+889d others(12): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974276 | |||||||
| chr1:211974276 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0143 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1815+876_1815+889d others(16): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974276 | |||||||
| chr1:211974276 | A | AATATATA others(9): Show |
1 | a0001c0001t0001g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1815+874_1815+889d others(18): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974276 | |||||||
| chr1:211974276 | A | T | 205 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(202): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1815+890T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974276 | |||||||
| chr1:211974308 | T | A | 20 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0003g0094 others(17): Show |
20 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1815+858A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974308 | |||||||
| chr1:211974308 | T | TATATATA others(3): Show |
1 | a0001c0001t0004g0128 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1815+857_1815+858i others(12): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974308 | |||||||
| chr1:211974308 | T | TATATATA others(7): Show |
1 | a0001c0001t0004g0129 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1815+857_1815+858i others(16): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974308 | |||||||
| chr1:211974308 | T | TATATATA others(15): Show |
1 | a0001c0001t0004g0125 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1815+857_1815+858i others(24): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974308 | |||||||
| chr1:211974309 | A | ATATATAT others(8): Show |
1 | a0001c0001t0002g0190 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1815+856_1815+857i others(17): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974309 | |||||||
| chr1:211974403 | G | A | 169 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(166): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1815+763C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974403 | |||||||
| chr1:211974621 | A | G | 2 | a0001c0005t0001g0076 a0001c0005t0001g0097 |
2 | NA18998.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1815+545T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974621 | |||||||
| chr1:211974681 | A | G | 1 | a0001c0001t0010g0184 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1815+485T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974681 | |||||||
| chr1:211974687 | G | A | 1 | a0001c0001t0005g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1815+479C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974687 | |||||||
| chr1:211974764 | C | T | 10 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1815+402G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974764 | |||||||
| chr1:211974925 | C | T | 1 | a0001c0001t0003g0273 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1815+241G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974925 | |||||||
| chr1:211975004 | A | G | 1 | a0001c0001t0002g0224 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1815+162T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211975004 | |||||||
| chr1:211975070 | G | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815+96C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211975070 | |||||||
| chr1:211975417 | G | A | 2 | a0001c0001t0003g0265 a0001c0001t0003g0266 |
2 | HG00621.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1609-45C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211975417 | |||||||
| chr1:211975657 | C | T | 13 | a0001c0001t0003g0017 a0001c0001t0003g0200 a0001c0001t0005g0001 others(10): Show |
20 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1609-285G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211975657 | |||||||
| chr1:211975784 | C | T | 2 | a0001c0001t0003g0265 a0001c0001t0003g0266 |
2 | HG00621.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1609-412G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211975784 | |||||||
| chr1:211975838 | G | A | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1609-466C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211975838 | |||||||
| chr1:211975957 | GT | G | 312 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(309): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1609-586delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211975957 | |||||||
| chr1:211976044 | T | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1608+538A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976044 | |||||||
| chr1:211976080 | G | A | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1608+502C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976080 | |||||||
| chr1:211976097 | C | T | 6 | a0001c0001t0009g0198 a0001c0001t0011g0202 a0001c0001t0011g0204 others(3): Show |
6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608+485G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976097 | |||||||
| chr1:211976098 | G | A | 4 | a0001c0001t0002g0218 a0001c0001t0002g0235 a0001c0001t0002g0240 others(1): Show |
4 | HG03688.hp2 HG03834.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+484C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976098 | |||||||
| chr1:211976195 | A | G | 6 | a0001c0001t0009g0198 a0001c0001t0011g0202 a0001c0001t0011g0204 others(3): Show |
6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608+387T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976195 | |||||||
| chr1:211976262 | G | A | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1608+320C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976262 | |||||||
| chr1:211976298 | C | T | 1 | a0001c0001t0004g0149 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1608+284G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976298 | |||||||
| chr1:211976334 | A | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1608+248T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976334 | |||||||
| chr1:211976357 | G | A | 45 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(42): Show |
49 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1608+225C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976357 | |||||||
| chr1:211976752 | C | A | 1 | a0001c0001t0004g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1471-33G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211976752 | |||||||
| chr1:211976804 | A | G | 1 | a0001c0002t0015g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1471-85T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211976804 | |||||||
| chr1:211976809 | G | C | 1 | a0001c0001t0003g0017 | 2 | HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1471-90C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211976809 | |||||||
| chr1:211976919 | G | T | 16 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1471-200C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211976919 | |||||||
| chr1:211977114 | G | C | 1 | a0001c0001t0002g0199 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1471-395C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977114 | |||||||
| chr1:211977387 | C | T | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1471-668G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977387 | |||||||
| chr1:211977388 | G | A | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1471-669C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977388 | |||||||
| chr1:211977422 | C | T | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1471-703G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977422 | |||||||
| chr1:211977612 | T | C | 6 | a0001c0001t0009g0198 a0001c0001t0011g0202 a0001c0001t0011g0204 others(3): Show |
6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470+660A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977612 | |||||||
| chr1:211977629 | T | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1470+643A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977629 | |||||||
| chr1:211977760 | C | T | 17 | a0001c0001t0003g0094 a0001c0001t0003g0163 a0001c0001t0003g0254 others(14): Show |
17 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1470+512G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977760 | |||||||
| chr1:211977784 | A | C | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1470+488T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977784 | |||||||
| chr1:211977892 | TA | T | 5 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0001c0001t0002g0244 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1470+379delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977892 | |||||||
| chr1:211977946 | A | G | 169 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(166): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1470+326T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977946 | |||||||
| chr1:211978174 | G | A | 2 | a0001c0006t0001g0102 a0001c0006t0001g0121 |
2 | NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1470+98C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211978174 | |||||||
| chr1:211978557 | G | C | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1231-46C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211978557 | |||||||
| chr1:211978572 | A | G | 2 | a0001c0001t0002g0178 a0001c0001t0002g0186 |
2 | HG00323.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1231-61T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211978572 | |||||||
| chr1:211978642 | A | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-131T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211978642 | |||||||
| chr1:211978702 | TAAC | T | 50 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0031 others(47): Show |
52 | HG00140.hp2 HG00597.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.1231-194_1231-192d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211978702 | |||||||
| chr1:211978831 | T | C | 224 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(221): Show |
245 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.1231-320A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211978831 | |||||||
| chr1:211978833 | A | C | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1231-322T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211978833 | |||||||
| chr1:211979335 | A | G | 3 | a0001c0001t0003g0278 a0001c0001t0003g0279 a0001c0001t0003g0280 |
3 | HG00738.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1231-824T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211979335 | |||||||
| chr1:211979437 | A | G | 11 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0166 others(8): Show |
11 | HG01433.hp1 HG02698.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1231-926T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211979437 | |||||||
| chr1:211979674 | C | T | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1231-1163G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211979674 | |||||||
| chr1:211979683 | A | G | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1231-1172T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211979683 | |||||||
| chr1:211980046 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1230+1047G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980046 | |||||||
| chr1:211980282 | T | C | 1 | a0001c0001t0003g0306 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1230+811A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980282 | |||||||
| chr1:211980317 | G | A | 1 | a0001c0001t0003g0263 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1230+776C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980317 | |||||||
| chr1:211980328 | T | C | 5 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0001c0001t0002g0244 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230+765A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980328 | |||||||
| chr1:211980480 | G | C | 5 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0001c0001t0002g0244 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230+613C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980480 | |||||||
| chr1:211980528 | C | T | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1230+565G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980528 | |||||||
| chr1:211980529 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+564C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980529 | |||||||
| chr1:211980720 | TGA | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230+371_1230+372d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980720 | |||||||
| chr1:211980842 | G | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230+251C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980842 | |||||||
| chr1:211980854 | T | C | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1230+239A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980854 | |||||||
| chr1:211980901 | C | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230+192G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980901 | |||||||
| chr1:211980999 | T | A | 2 | a0001c0001t0003g0278 a0001c0001t0003g0279 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1230+94A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980999 | |||||||
| chr1:211981045 | A | G | 7 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(4): Show |
11 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1230+48T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211981045 | |||||||
| chr1:211981346 | C | T | 3 | a0001c0001t0002g0178 a0001c0001t0002g0186 a0001c0001t0002g0193 |
3 | HG00323.hp1 HG00733.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1133-156G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981346 | |||||||
| chr1:211981369 | TAA | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1133-181_1133-180d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981369 | |||||||
| chr1:211981536 | G | A | 3 | a0001c0001t0010g0184 a0001c0001t0010g0185 a0001c0001t0010g0189 |
3 | NA18979.hp1 NA18994.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1133-346C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981536 | |||||||
| chr1:211981588 | A | G | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1133-398T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981588 | |||||||
| chr1:211981666 | T | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1133-476A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981666 | |||||||
| chr1:211981721 | A | G | 1 | a0001c0002t0009g0033 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1133-531T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981721 | |||||||
| chr1:211981850 | A | G | 19 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(16): Show |
19 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1133-660T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981850 | |||||||
| chr1:211981945 | G | A | 17 | a0001c0001t0003g0094 a0001c0001t0003g0163 a0001c0001t0003g0254 others(14): Show |
17 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1132+731C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981945 | |||||||
| chr1:211982019 | G | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1132+657C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211982019 | |||||||
| chr1:211982107 | T | C | 1 | a0001c0001t0003g0309 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1132+569A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211982107 | |||||||
| chr1:211982178 | G | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1132+498C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211982178 | |||||||
| chr1:211982317 | T | C | 2 | a0001c0001t0001g0052 a0005c0009t0001g0053 |
2 | NA18941.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1132+359A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211982317 | |||||||
| chr1:211982833 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0070 |
2 | HG00099.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.998-23A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211982833 | |||||||
| chr1:211982913 | A | G | 2 | a0001c0001t0003g0265 a0001c0001t0003g0266 |
2 | HG00621.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.998-103T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211982913 | |||||||
| chr1:211982958 | A | C | 2 | a0002c0003t0007g0316 a0002c0003t0007g0317 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.998-148T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211982958 | |||||||
| chr1:211982986 | T | C | 1 | a0001c0001t0002g0268 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.998-176A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211982986 | |||||||
| chr1:211983055 | AT | A | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.998-246delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983055 | |||||||
| chr1:211983374 | C | A | 4 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.998-564G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983374 | |||||||
| chr1:211983712 | G | A | 2 | a0002c0003t0007g0316 a0002c0003t0007g0317 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.998-902C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983712 | |||||||
| chr1:211983855 | G | GT | 134 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(131): Show |
146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.998-1046dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983855 | |||||||
| chr1:211983860 | T | G | 1 | a0001c0001t0003g0309 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.998-1050A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983860 | |||||||
| chr1:211983968 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.998-1158C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983968 | |||||||
| chr1:211983982 | A | G | 1 | a0001c0001t0003g0303 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.998-1172T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983982 | |||||||
| chr1:211983999 | G | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.998-1189C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983999 | |||||||
| chr1:211984016 | A | G | 14 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0001c0001t0001g0056 others(11): Show |
14 | HG00423.hp1 HG00558.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.998-1206T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984016 | |||||||
| chr1:211984188 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.998-1378T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984188 | |||||||
| chr1:211984349 | A | ACT | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.998-1541_998-1540d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984349 | |||||||
| chr1:211984501 | T | C | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.998-1691A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984501 | |||||||
| chr1:211984518 | T | C | 2 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
2 | HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.998-1708A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984518 | |||||||
| chr1:211984520 | C | T | 2 | a0002c0003t0007g0316 a0002c0003t0007g0317 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.998-1710G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984520 | |||||||
| chr1:211984633 | T | G | 1 | a0001c0001t0001g0038 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.998-1823A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984633 | |||||||
| chr1:211984659 | A | T | 3 | a0001c0001t0003g0002 a0001c0001t0003g0306 a0001c0001t0018g0305 |
6 | HG00733.hp1 HG01074.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.998-1849T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984659 | |||||||
| chr1:211984712 | C | A | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.998-1902G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984712 | |||||||
| chr1:211984812 | CTTGTT | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.998-2007_998-2003d others(7): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984812 | |||||||
| chr1:211984914 | T | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.998-2104A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984914 | |||||||
| chr1:211985374 | A | C | 134 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(131): Show |
146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.997+2512T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211985374 | |||||||
| chr1:211985569 | C | A | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.997+2317G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211985569 | |||||||
| chr1:211985641 | G | A | 1 | a0001c0001t0003g0167 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.997+2245C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211985641 | |||||||
| chr1:211985676 | G | C | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.997+2210C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211985676 | |||||||
| chr1:211985736 | T | C | 2 | a0001c0001t0003g0278 a0001c0001t0003g0279 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.997+2150A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211985736 | |||||||
| chr1:211985744 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.997+2142G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211985744 | |||||||
| chr1:211985930 | C | A | 169 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(166): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.997+1956G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211985930 | |||||||
| chr1:211986063 | T | C | 2 | a0001c0001t0003g0271 a0001c0001t0003g0272 |
2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.997+1823A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211986063 | |||||||
| chr1:211986485 | G | C | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.997+1401C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211986485 | |||||||
| chr1:211986540 | T | C | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.997+1346A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211986540 | |||||||
| chr1:211986643 | T | A | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.997+1243A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211986643 | |||||||
| chr1:211986755 | G | T | 3 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0134 |
3 | HG00741.hp1 HG02738.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.997+1131C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211986755 | |||||||
| chr1:211986813 | T | C | 3 | a0001c0001t0003g0310 a0001c0001t0003g0311 a0001c0001t0003g0312 |
3 | HG02257.hp2 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.997+1073A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211986813 | |||||||
| chr1:211986903 | C | T | 1 | a0001c0004t0022g0322 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.997+983G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211986903 | |||||||
| chr1:211987318 | C | A | 93 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(90): Show |
101 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.997+568G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211987318 | |||||||
| chr1:211987321 | A | C | 1 | a0001c0001t0003g0309 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.997+565T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211987321 | |||||||
| chr1:211987328 | C | A | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.997+558G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211987328 | |||||||
| chr1:211987487 | T | C | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.997+399A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211987487 | |||||||
| chr1:211987685 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.997+201A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211987685 | |||||||
| chr1:211987788 | C | T | 1 | a0001c0001t0002g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.997+98G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211987788 | |||||||
| chr1:211988130 | A | T | 1 | a0001c0001t0002g0196 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.880-127T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988130 | |||||||
| chr1:211988182 | G | A | 1 | a0001c0001t0002g0194 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.880-179C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988182 | |||||||
| chr1:211988186 | G | A | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-183C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988186 | |||||||
| chr1:211988364 | A | G | 16 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.880-361T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988364 | |||||||
| chr1:211988398 | G | C | 1 | a0001c0001t0002g0221 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.880-395C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988398 | |||||||
| chr1:211988421 | C | CA | 15 | a0001c0001t0002g0178 a0001c0001t0002g0186 a0001c0001t0002g0243 others(12): Show |
21 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.880-419dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988421 | |||||||
| chr1:211988429 | A | AG | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.880-427_880-426ins others(1): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988429 | |||||||
| chr1:211988434 | A | C | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.880-431T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988434 | |||||||
| chr1:211988563 | T | C | 1 | a0001c0001t0003g0275 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.880-560A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988563 | |||||||
| chr1:211988596 | T | C | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.880-593A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988596 | |||||||
| chr1:211988597 | T | C | 1 | a0001c0001t0002g0191 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.880-594A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988597 | |||||||
| chr1:211988657 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.880-654C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988657 | |||||||
| chr1:211988681 | C | T | 1 | a0001c0001t0002g0015 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.880-678G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988681 | |||||||
| chr1:211988887 | T | C | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-884A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988887 | |||||||
| chr1:211989009 | A | G | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-1006T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989009 | |||||||
| chr1:211989059 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.880-1056T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989059 | |||||||
| chr1:211989163 | T | C | 4 | a0001c0001t0002g0014 a0001c0001t0002g0176 a0001c0001t0002g0187 others(1): Show |
5 | HG01192.hp2 HG01361.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-1160A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989163 | |||||||
| chr1:211989379 | G | GTT | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.880-1378_880-1377d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989379 | |||||||
| chr1:211989481 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.880-1478G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989481 | |||||||
| chr1:211989588 | G | A | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-1585C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989588 | |||||||
| chr1:211989638 | A | G | 21 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0060 others(18): Show |
23 | HG01168.hp1 HG01175.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.880-1635T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989638 | |||||||
| chr1:211989694 | C | T | 1 | a0003c0008t0002g0223 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.880-1691G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989694 | |||||||
| chr1:211989745 | C | A | 4 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-1742G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989745 | |||||||
| chr1:211989821 | C | CA | 10 | a0001c0001t0001g0062 a0001c0001t0001g0100 a0001c0001t0002g0209 others(7): Show |
10 | HG02129.hp2 HG02572.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.880-1819dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989821 | |||||||
| chr1:211989821 | CA | C | 9 | a0001c0001t0002g0179 a0001c0001t0003g0295 a0001c0004t0007g0320 others(6): Show |
9 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-1819delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989821 | |||||||
| chr1:211990064 | G | A | 16 | a0001c0001t0003g0017 a0001c0001t0003g0200 a0001c0001t0005g0001 others(13): Show |
23 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.880-2061C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990064 | |||||||
| chr1:211990285 | TA | T | 82 | a0001c0001t0001g0145 a0001c0001t0002g0281 a0001c0001t0003g0002 others(79): Show |
93 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.880-2283delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990285 | |||||||
| chr1:211990285 | TAA | T | 89 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(86): Show |
97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.880-2284_880-2283d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990285 | |||||||
| chr1:211990304 | G | A | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.880-2301C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990304 | |||||||
| chr1:211990330 | T | C | 1 | a0001c0004t0007g0320 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.880-2327A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990330 | |||||||
| chr1:211990341 | T | C | 1 | a0001c0001t0003g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.880-2338A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990341 | |||||||
| chr1:211990522 | C | T | 2 | a0002c0003t0020g0318 a0002c0007t0021g0319 |
2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.880-2519G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990522 | |||||||
| chr1:211990549 | T | C | 1 | a0001c0001t0008g0037 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.880-2546A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990549 | |||||||
| chr1:211990708 | T | C | 1 | a0001c0001t0002g0194 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.880-2705A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990708 | |||||||
| chr1:211990757 | G | C | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-2754C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990757 | |||||||
| chr1:211990780 | T | C | 1 | a0001c0001t0002g0246 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.880-2777A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990780 | |||||||
| chr1:211991086 | C | T | 4 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-3083G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211991086 | |||||||
| chr1:211991210 | T | C | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-3207A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211991210 | |||||||
| chr1:211991460 | T | A | 1 | a0001c0001t0002g0268 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.880-3457A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211991460 | |||||||
| chr1:211991801 | C | G | 30 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(27): Show |
34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.880-3798G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211991801 | |||||||
| chr1:211991978 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.880-3975C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211991978 | |||||||
| chr1:211992117 | G | A | 1 | a0001c0001t0003g0273 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.880-4114C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992117 | |||||||
| chr1:211992293 | G | A | 189 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(186): Show |
208 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.880-4290C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992293 | |||||||
| chr1:211992465 | A | C | 1 | a0001c0001t0003g0273 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.880-4462T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992465 | |||||||
| chr1:211992491 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.880-4488C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992491 | |||||||
| chr1:211992639 | T | C | 44 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(41): Show |
48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.880-4636A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992639 | |||||||
| chr1:211992704 | A | T | 1 | a0001c0001t0001g0072 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.880-4701T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992704 | |||||||
| chr1:211992714 | G | A | 1 | a0001c0001t0005g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.880-4711C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992714 | |||||||
| chr1:211992753 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.880-4750C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992753 | |||||||
| chr1:211992781 | A | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-4778T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992781 | |||||||
| chr1:211993180 | C | A | 1 | a0001c0001t0001g0099 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.880-5177G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993180 | |||||||
| chr1:211993408 | G | A | 1 | a0004c0011t0001g0043 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.880-5405C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993408 | |||||||
| chr1:211993506 | T | C | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.880-5503A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993506 | |||||||
| chr1:211993508 | T | C | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.880-5505A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993508 | |||||||
| chr1:211993510 | T | C | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.880-5507A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993510 | |||||||
| chr1:211993525 | C | CA | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.880-5523dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993525 | |||||||
| chr1:211993532 | T | C | 1 | a0001c0001t0002g0231 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.880-5529A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993532 | |||||||
| chr1:211993537 | A | G | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.880-5534T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993537 | |||||||
| chr1:211993538 | G | A | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.880-5535C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993538 | |||||||
| chr1:211993540 | C | T | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.880-5537G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993540 | |||||||
| chr1:211993541 | G | A | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.880-5538C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993541 | |||||||
| chr1:211993579 | C | G | 44 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(41): Show |
48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.880-5576G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993579 | |||||||
| chr1:211993658 | T | C | 19 | a0001c0001t0003g0021 a0001c0001t0003g0197 a0001c0001t0003g0252 others(16): Show |
19 | HG00323.hp2 HG00642.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.880-5655A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993658 | |||||||
| chr1:211993679 | C | CA | 10 | a0001c0001t0001g0118 a0001c0001t0001g0140 a0001c0001t0002g0015 others(7): Show |
12 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.880-5677dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993679 | |||||||
| chr1:211993679 | C | CAAAA | 6 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0002c0003t0007g0316 others(3): Show |
6 | HG02257.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-5680_880-5677d others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993679 | |||||||
| chr1:211993679 | CA | C | 7 | a0001c0001t0001g0056 a0001c0001t0001g0071 a0001c0001t0001g0139 others(4): Show |
7 | HG03041.hp1 HG03491.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-5677delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993679 | |||||||
| chr1:211993833 | T | C | 1 | a0001c0001t0003g0261 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.880-5830A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993833 | |||||||
| chr1:211993834 | C | T | 10 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-5831G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993834 | |||||||
| chr1:211993848 | G | A | 134 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(131): Show |
146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.880-5845C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993848 | |||||||
| chr1:211994000 | A | G | 16 | a0001c0001t0003g0017 a0001c0001t0003g0200 a0001c0001t0005g0001 others(13): Show |
23 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.880-5997T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994000 | |||||||
| chr1:211994152 | C | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-6149G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994152 | |||||||
| chr1:211994232 | G | T | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-6229C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994232 | |||||||
| chr1:211994423 | C | CT | 55 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0208 others(52): Show |
56 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.880-6421dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994423 | |||||||
| chr1:211994423 | C | CTT | 4 | a0001c0001t0002g0206 a0001c0001t0003g0002 a0001c0001t0003g0306 others(1): Show |
7 | HG00733.hp1 HG01074.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-6422_880-6421d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994423 | |||||||
| chr1:211994423 | CT | C | 16 | a0001c0001t0001g0068 a0001c0001t0002g0236 a0001c0001t0003g0017 others(13): Show |
23 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.880-6421delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994423 | |||||||
| chr1:211994434 | T | C | 3 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0134 |
3 | HG00741.hp1 HG02738.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.880-6431A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994434 | |||||||
| chr1:211994450 | T | A | 16 | a0001c0001t0003g0017 a0001c0001t0003g0200 a0001c0001t0005g0001 others(13): Show |
23 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.880-6447A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994450 | |||||||
| chr1:211994676 | G | A | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.880-6673C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994676 | |||||||
| chr1:211994686 | G | A | 1 | a0001c0004t0007g0321 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.880-6683C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994686 | |||||||
| chr1:211994764 | A | T | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.880-6761T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994764 | |||||||
| chr1:211994797 | A | G | 1 | a0001c0001t0003g0308 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.880-6794T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994797 | |||||||
| chr1:211994807 | C | T | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-6804G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994807 | |||||||
| chr1:211994844 | CAAGAT | C | 3 | a0001c0001t0011g0202 a0001c0001t0011g0204 a0001c0001t0019g0203 |
3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.880-6846_880-6842d others(7): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994844 | |||||||
| chr1:211994886 | G | GA | 234 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0089 others(231): Show |
257 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.880-6884dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994886 | |||||||
| chr1:211995115 | ATTTTCAT | A | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-7119_880-7113d others(9): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995115 | |||||||
| chr1:211995124 | C | G | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-7121G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995124 | |||||||
| chr1:211995225 | G | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-7222C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995225 | |||||||
| chr1:211995331 | C | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-7328G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995331 | |||||||
| chr1:211995367 | A | C | 1 | a0001c0001t0003g0263 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.880-7364T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995367 | |||||||
| chr1:211995373 | TTTTC | T | 4 | a0001c0001t0002g0245 a0001c0001t0003g0197 a0001c0001t0003g0252 others(1): Show |
4 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-7374_880-7371d others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995373 | |||||||
| chr1:211995530 | AT | A | 45 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(42): Show |
49 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.880-7528delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995530 | |||||||
| chr1:211995674 | C | T | 1 | a0001c0001t0003g0280 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.880-7671G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995674 | |||||||
| chr1:211995692 | A | C | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.880-7689T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995692 | |||||||
| chr1:211995828 | A | G | 17 | a0001c0001t0003g0094 a0001c0001t0003g0163 a0001c0001t0003g0254 others(14): Show |
17 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.880-7825T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995828 | |||||||
| chr1:211996053 | GA | G | 4 | a0001c0001t0001g0139 a0001c0001t0011g0202 a0001c0001t0011g0204 others(1): Show |
4 | HG02572.hp2 HG03579.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-8051delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996053 | |||||||
| chr1:211996150 | G | A | 34 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(31): Show |
40 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.880-8147C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996150 | |||||||
| chr1:211996243 | G | A | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-8240C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996243 | |||||||
| chr1:211996296 | G | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-8293C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996296 | |||||||
| chr1:211996384 | A | T | 320 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(317): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.880-8381T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996384 | |||||||
| chr1:211996471 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.880-8468G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996471 | |||||||
| chr1:211996705 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.880-8702C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996705 | |||||||
| chr1:211996722 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.880-8719A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996722 | |||||||
| chr1:211996750 | C | A | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.880-8747G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996750 | |||||||
| chr1:211996791 | C | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-8788G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996791 | |||||||
| chr1:211996815 | A | C | 1 | a0001c0004t0022g0322 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.880-8812T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996815 | |||||||
| chr1:211996925 | G | A | 3 | a0001c0001t0003g0310 a0001c0001t0003g0311 a0001c0001t0003g0312 |
3 | HG02257.hp2 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.880-8922C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996925 | |||||||
| chr1:211996938 | C | T | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.880-8935G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996938 | |||||||
| chr1:211996968 | G | A | 2 | a0002c0003t0020g0318 a0002c0007t0021g0319 |
2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.880-8965C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996968 | |||||||
| chr1:211997335 | C | G | 1 | a0001c0001t0001g0139 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.879+9304G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997335 | |||||||
| chr1:211997336 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.879+9303C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997336 | |||||||
| chr1:211997400 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.879+9239C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997400 | |||||||
| chr1:211997471 | T | C | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.879+9168A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997471 | |||||||
| chr1:211997528 | G | GA | 111 | a0001c0001t0001g0069 a0001c0001t0001g0091 a0001c0001t0002g0011 others(108): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.879+9110dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997528 | |||||||
| chr1:211997528 | G | GAA | 13 | a0001c0001t0002g0031 a0001c0001t0002g0172 a0001c0001t0002g0187 others(10): Show |
13 | HG00423.hp2 HG01361.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.879+9109_879+9110d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997528 | |||||||
| chr1:211997528 | GA | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0139 others(4): Show |
7 | HG00140.hp1 HG01109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+9110delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997528 | |||||||
| chr1:211997528 | GAAAAAAA others(1): Show |
G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+9103_879+9110d others(10): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997528 | |||||||
| chr1:211997550 | A | G | 15 | a0001c0001t0003g0163 a0001c0001t0003g0254 a0001c0001t0003g0255 others(12): Show |
15 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.879+9089T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997550 | |||||||
| chr1:211997551 | G | A | 134 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(131): Show |
146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.879+9088C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997551 | |||||||
| chr1:211997622 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.879+9017A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997622 | |||||||
| chr1:211997694 | CA | C | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.879+8944delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997694 | |||||||
| chr1:211997696 | T | G | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.879+8943A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997696 | |||||||
| chr1:211997708 | A | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+8931T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997708 | |||||||
| chr1:211997725 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.879+8914T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997725 | |||||||
| chr1:211997793 | G | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+8846C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997793 | |||||||
| chr1:211997878 | C | CA | 15 | a0001c0001t0001g0092 a0001c0001t0002g0187 a0001c0001t0002g0232 others(12): Show |
15 | HG00544.hp2 HG00597.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.879+8760dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997878 | |||||||
| chr1:211997878 | CA | C | 6 | a0001c0001t0001g0068 a0001c0001t0001g0139 a0001c0001t0002g0178 others(3): Show |
6 | HG00323.hp1 HG02280.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.879+8760delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997878 | |||||||
| chr1:211997936 | T | C | 3 | a0001c0001t0003g0278 a0001c0001t0003g0279 a0001c0001t0003g0280 |
3 | HG00738.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.879+8703A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997936 | |||||||
| chr1:211998068 | G | A | 4 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+8571C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998068 | |||||||
| chr1:211998266 | C | T | 2 | a0001c0001t0004g0314 a0001c0001t0004g0315 |
2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.879+8373G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998266 | |||||||
| chr1:211998281 | G | A | 1 | a0001c0001t0003g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.879+8358C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998281 | |||||||
| chr1:211998337 | A | G | 33 | a0001c0001t0002g0018 a0001c0001t0002g0031 a0001c0001t0002g0199 others(30): Show |
34 | HG00597.hp2 HG01346.hp1 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.879+8302T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998337 | |||||||
| chr1:211998366 | T | C | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.879+8273A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998366 | |||||||
| chr1:211998446 | A | G | 3 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0037 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.879+8193T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998446 | |||||||
| chr1:211998535 | T | C | 6 | a0001c0001t0003g0020 a0001c0001t0003g0286 a0001c0001t0003g0295 others(3): Show |
7 | NA18939.hp1 NA18950.hp2 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+8104A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998535 | |||||||
| chr1:211998614 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.879+8025A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998614 | |||||||
| chr1:211998654 | CCTATAAA others(39): Show |
C | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.879+7939_879+7984d others(48): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998654 | |||||||
| chr1:211998806 | CAA | C | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.879+7831_879+7832d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998806 | |||||||
| chr1:211998809 | TAAC | T | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.879+7827_879+7829d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998809 | |||||||
| chr1:211998978 | T | C | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.879+7661A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998978 | |||||||
| chr1:211999007 | A | T | 4 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(1): Show |
4 | HG02080.hp2 NA18612.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+7632T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999007 | |||||||
| chr1:211999051 | C | T | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.879+7588G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999051 | |||||||
| chr1:211999421 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.879+7218G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999421 | |||||||
| chr1:211999471 | A | G | 1 | a0001c0004t0007g0320 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.879+7168T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999471 | |||||||
| chr1:211999475 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.879+7164C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999475 | |||||||
| chr1:211999477 | C | T | 2 | a0001c0001t0004g0050 a0001c0001t0004g0051 |
2 | HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.879+7162G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999477 | |||||||
| chr1:211999533 | T | C | 1 | a0001c0001t0003g0252 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.879+7106A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999533 | |||||||
| chr1:211999585 | A | C | 1 | a0001c0001t0008g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.879+7054T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999585 | |||||||
| chr1:211999669 | C | T | 1 | a0001c0001t0003g0287 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.879+6970G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999669 | |||||||
| chr1:211999693 | G | A | 30 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(27): Show |
34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.879+6946C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999693 | |||||||
| chr1:211999790 | G | A | 2 | a0001c0004t0007g0320 a0001c0004t0007g0321 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.879+6849C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999790 | |||||||
| chr1:211999806 | G | A | 189 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(186): Show |
208 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.879+6833C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999806 | |||||||
| chr1:211999825 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.879+6814G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999825 | |||||||
| chr1:211999877 | C | G | 16 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.879+6762G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999877 | |||||||
| chr1:211999877 | C | T | 5 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0001c0001t0002g0244 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+6762G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999877 | |||||||
| chr1:211999895 | TG | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+6743delC | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999895 | |||||||
| chr1:211999975 | C | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+6664G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999975 | |||||||
| chr1:211999975 | C | G | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.879+6664G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999975 | |||||||
| chr1:212000030 | T | G | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.879+6609A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000030 | |||||||
| chr1:212000202 | G | A | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.879+6437C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000202 | |||||||
| chr1:212000255 | G | A | 2 | a0002c0003t0020g0318 a0002c0007t0021g0319 |
2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.879+6384C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000255 | |||||||
| chr1:212000256 | G | A | 17 | a0001c0001t0003g0094 a0001c0001t0003g0163 a0001c0001t0003g0254 others(14): Show |
17 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.879+6383C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000256 | |||||||
| chr1:212000346 | C | T | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.879+6293G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000346 | |||||||
| chr1:212000514 | C | T | 1 | a0001c0001t0003g0254 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.879+6125G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000514 | |||||||
| chr1:212000687 | C | T | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.879+5952G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000687 | |||||||
| chr1:212000783 | C | T | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+5856G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000783 | |||||||
| chr1:212000865 | T | C | 3 | a0001c0001t0003g0278 a0001c0001t0003g0279 a0001c0001t0003g0280 |
3 | HG00738.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.879+5774A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000865 | |||||||
| chr1:212001004 | CA | C | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.879+5634delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001004 | |||||||
| chr1:212001064 | C | CT | 17 | a0001c0001t0004g0009 a0001c0001t0004g0063 a0001c0001t0004g0103 others(14): Show |
18 | HG01168.hp1 HG01175.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.879+5574dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001064 | |||||||
| chr1:212001064 | CT | C | 28 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0002g0247 others(25): Show |
28 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.879+5574delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001064 | |||||||
| chr1:212001064 | CTT | C | 154 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(151): Show |
173 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.879+5573_879+5574d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001064 | |||||||
| chr1:212001064 | CTTT | C | 6 | a0001c0001t0003g0278 a0001c0001t0003g0279 a0001c0001t0003g0280 others(3): Show |
6 | HG00323.hp2 HG00738.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+5572_879+5574d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001064 | |||||||
| chr1:212001158 | C | G | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.879+5481G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001158 | |||||||
| chr1:212001228 | C | T | 5 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0001c0001t0002g0244 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+5411G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001228 | |||||||
| chr1:212001358 | C | T | 5 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0001c0001t0002g0244 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+5281G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001358 | |||||||
| chr1:212001400 | G | A | 2 | a0002c0003t0007g0316 a0002c0003t0007g0317 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.879+5239C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001400 | |||||||
| chr1:212002099 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0070 |
2 | HG00099.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.879+4540G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002099 | |||||||
| chr1:212002251 | T | C | 5 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0001c0001t0002g0244 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+4388A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002251 | |||||||
| chr1:212002429 | A | G | 1 | a0001c0001t0002g0019 | 2 | NA18944.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.879+4210T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002429 | |||||||
| chr1:212002451 | C | T | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.879+4188G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002451 | |||||||
| chr1:212002473 | C | G | 1 | a0001c0001t0010g0189 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.879+4166G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002473 | |||||||
| chr1:212002478 | T | C | 1 | a0001c0001t0004g0050 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.879+4161A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002478 | |||||||
| chr1:212002717 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.879+3922G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002717 | |||||||
| chr1:212002786 | C | T | 3 | a0001c0001t0003g0310 a0001c0001t0003g0311 a0001c0001t0003g0312 |
3 | HG02257.hp2 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.879+3853G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002786 | |||||||
| chr1:212002795 | G | A | 1 | a0001c0001t0006g0155 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.879+3844C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002795 | |||||||
| chr1:212003136 | C | T | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.879+3503G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003136 | |||||||
| chr1:212003155 | T | C | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.879+3484A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003155 | |||||||
| chr1:212003227 | C | T | 44 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(41): Show |
48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.879+3412G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003227 | |||||||
| chr1:212003305 | C | CA | 33 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0096 others(30): Show |
33 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.879+3333dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003305 | |||||||
| chr1:212003305 | CA | C | 21 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0157 others(18): Show |
21 | HG00741.hp1 HG01109.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.879+3333delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003305 | |||||||
| chr1:212003305 | CAAA | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+3331_879+3333d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003305 | |||||||
| chr1:212003423 | G | C | 84 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(81): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.879+3216C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003423 | |||||||
| chr1:212003490 | CCA | C | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.879+3147_879+3148d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003490 | |||||||
| chr1:212003712 | A | C | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.879+2927T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003712 | |||||||
| chr1:212003868 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.879+2771T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003868 | |||||||
| chr1:212003913 | G | C | 1 | a0001c0001t0019g0203 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.879+2726C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003913 | |||||||
| chr1:212004056 | C | A | 1 | a0001c0001t0003g0258 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.879+2583G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004056 | |||||||
| chr1:212004233 | T | C | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.879+2406A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004233 | |||||||
| chr1:212004362 | C | A | 2 | a0001c0001t0003g0265 a0001c0001t0003g0266 |
2 | HG00621.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.879+2277G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004362 | |||||||
| chr1:212004479 | T | C | 1 | a0001c0001t0002g0188 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.879+2160A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004479 | |||||||
| chr1:212004507 | C | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+2132G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004507 | |||||||
| chr1:212004520 | T | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+2119A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004520 | |||||||
| chr1:212004670 | T | C | 84 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(81): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.879+1969A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004670 | |||||||
| chr1:212004820 | C | A | 1 | a0001c0001t0003g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.879+1819G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004820 | |||||||
| chr1:212004875 | C | T | 1 | a0001c0001t0003g0262 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.879+1764G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004875 | |||||||
| chr1:212004904 | C | T | 4 | a0001c0001t0003g0282 a0001c0001t0003g0288 a0001c0001t0003g0289 others(1): Show |
4 | HG00423.hp2 NA18747.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+1735G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004904 | |||||||
| chr1:212004921 | C | T | 34 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(31): Show |
40 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.879+1718G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004921 | |||||||
| chr1:212004965 | G | C | 1 | a0001c0001t0003g0309 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.879+1674C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004965 | |||||||
| chr1:212004970 | C | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+1669G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004970 | |||||||
| chr1:212005117 | C | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 |
3 | HG00738.hp2 HG00741.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.879+1522G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005117 | |||||||
| chr1:212005151 | T | C | 2 | a0001c0001t0003g0283 a0001c0001t0003g0285 |
2 | NA18972.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.879+1488A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005151 | |||||||
| chr1:212005371 | G | A | 1 | a0001c0001t0010g0189 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.879+1268C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005371 | |||||||
| chr1:212005454 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.879+1185A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005454 | |||||||
| chr1:212005479 | A | G | 3 | a0001c0001t0011g0202 a0001c0001t0011g0204 a0001c0001t0019g0203 |
3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.879+1160T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005479 | |||||||
| chr1:212005482 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.879+1157G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005482 | |||||||
| chr1:212005623 | C | G | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.879+1016G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005623 | |||||||
| chr1:212005628 | T | C | 3 | a0001c0001t0003g0310 a0001c0001t0003g0311 a0001c0001t0003g0312 |
3 | HG02257.hp2 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.879+1011A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005628 | |||||||
| chr1:212005837 | C | T | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.879+802G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005837 | |||||||
| chr1:212006059 | A | G | 1 | a0001c0001t0002g0248 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.879+580T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212006059 | |||||||
| chr1:212006398 | G | A | 10 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.879+241C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212006398 | |||||||
| chr1:212006853 | A | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.757-92T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 6/19 | chr1 | 212006853 | |||||||
| chr1:212006980 | G | T | 3 | a0001c0001t0003g0287 a0001c0001t0003g0307 a0001c0001t0003g0308 |
3 | HG00544.hp2 HG00597.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.757-219C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 6/19 | chr1 | 212006980 | |||||||
| chr1:212007079 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.756+171C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 6/19 | chr1 | 212007079 | |||||||
| chr1:212007114 | A | G | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.756+136T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 6/19 | chr1 | 212007114 | |||||||
| chr1:212007231 | T | C | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.756+19A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 6/19 | chr1 | 212007231 | |||||||
| chr1:212007519 | G | A | 1 | a0001c0001t0003g0163 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.557-70C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212007519 | |||||||
| chr1:212007570 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.557-121A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212007570 | |||||||
| chr1:212007774 | C | T | 1 | a0001c0001t0002g0173 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.557-325G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212007774 | |||||||
| chr1:212008127 | T | C | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.557-678A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212008127 | |||||||
| chr1:212008148 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.557-699G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212008148 | |||||||
| chr1:212008149 | G | A | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.557-700C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212008149 | |||||||
| chr1:212008183 | C | T | 1 | a0001c0001t0003g0309 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.557-734G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212008183 | |||||||
| chr1:212008524 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.557-1075C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212008524 | |||||||
| chr1:212008643 | A | C | 89 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(86): Show |
97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.557-1194T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212008643 | |||||||
| chr1:212008891 | G | T | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG01168.hp1 HG01175.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.557-1442C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212008891 | |||||||
| chr1:212009248 | T | G | 1 | a0001c0001t0002g0239 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.557-1799A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009248 | |||||||
| chr1:212009275 | T | C | 1 | a0001c0001t0004g0125 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.557-1826A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009275 | |||||||
| chr1:212009400 | C | T | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.557-1951G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009400 | |||||||
| chr1:212009455 | T | C | 21 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0060 others(18): Show |
23 | HG01168.hp1 HG01175.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.556+1920A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009455 | |||||||
| chr1:212009515 | C | G | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.556+1860G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009515 | |||||||
| chr1:212009583 | T | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.556+1792A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009583 | |||||||
| chr1:212009753 | G | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.556+1622C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009753 | |||||||
| chr1:212009772 | T | TC | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.556+1602dupG | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009772 | |||||||
| chr1:212009812 | A | C | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.556+1563T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009812 | |||||||
| chr1:212009821 | T | G | 7 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.556+1554A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009821 | |||||||
| chr1:212009839 | T | C | 1 | a0001c0001t0003g0254 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.556+1536A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009839 | |||||||
| chr1:212009878 | G | A | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.556+1497C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009878 | |||||||
| chr1:212009965 | T | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.556+1410A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009965 | |||||||
| chr1:212009984 | C | T | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.556+1391G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009984 | |||||||
| chr1:212010155 | G | A | 169 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(166): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.556+1220C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010155 | |||||||
| chr1:212010180 | A | G | 169 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(166): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.556+1195T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010180 | |||||||
| chr1:212010237 | G | C | 1 | a0001c0001t0002g0241 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.556+1138C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010237 | |||||||
| chr1:212010304 | G | A | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.556+1071C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010304 | |||||||
| chr1:212010346 | G | A | 44 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(41): Show |
48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.556+1029C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010346 | |||||||
| chr1:212010420 | T | C | 1 | a0001c0001t0004g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.556+955A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010420 | |||||||
| chr1:212010752 | T | C | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.556+623A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010752 | |||||||
| chr1:212010808 | T | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.556+567A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010808 | |||||||
| chr1:212010875 | C | T | 5 | a0001c0001t0004g0045 a0001c0001t0004g0046 a0001c0001t0004g0047 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.556+500G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010875 | |||||||
| chr1:212010907 | C | G | 3 | a0001c0001t0011g0202 a0001c0001t0011g0204 a0001c0001t0019g0203 |
3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.556+468G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010907 | |||||||
| chr1:212011133 | G | A | 2 | a0001c0001t0001g0160 a0006c0012t0001g0156 |
2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.556+242C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212011133 | |||||||
| chr1:212011164 | CCT | C | 3 | a0001c0001t0003g0017 a0001c0001t0003g0200 a0001c0001t0013g0270 |
4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.556+209_556+210del others(2): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212011164 | |||||||
| chr1:212011236 | C | T | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.556+139G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212011236 | |||||||
| chr1:212011442 | GAACAGAA | G | 4 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-28_510-22delTT others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212011442 | |||||||
| chr1:212011467 | A | T | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.510-46T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212011467 | |||||||
| chr1:212011524 | T | C | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-103A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212011524 | |||||||
| chr1:212011715 | T | G | 1 | a0001c0001t0002g0190 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.510-294A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212011715 | |||||||
| chr1:212011869 | T | C | 2 | a0001c0001t0002g0016 a0001c0001t0002g0191 |
3 | HG00639.hp1 HG02622.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.510-448A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212011869 | |||||||
| chr1:212012003 | T | C | 16 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.510-582A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012003 | |||||||
| chr1:212012106 | G | A | 2 | a0001c0006t0001g0102 a0001c0006t0001g0121 |
2 | NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.510-685C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012106 | |||||||
| chr1:212012251 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.510-830A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012251 | |||||||
| chr1:212012267 | G | A | 1 | a0001c0001t0003g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.510-846C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012267 | |||||||
| chr1:212012474 | G | A | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-1053C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012474 | |||||||
| chr1:212012679 | A | G | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.510-1258T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012679 | |||||||
| chr1:212012777 | T | A | 224 | a0001c0001t0001g0056 a0001c0001t0001g0136 a0001c0001t0002g0011 others(221): Show |
245 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.510-1356A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012777 | |||||||
| chr1:212012778 | T | C | 224 | a0001c0001t0001g0056 a0001c0001t0001g0136 a0001c0001t0002g0011 others(221): Show |
245 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.510-1357A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012778 | |||||||
| chr1:212012863 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510-1442G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012863 | |||||||
| chr1:212012884 | CAAATTTA others(6): Show |
C | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.510-1476_510-1464d others(15): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012884 | |||||||
| chr1:212012911 | A | G | 31 | a0001c0001t0001g0056 a0001c0001t0002g0281 a0001c0001t0003g0002 others(28): Show |
35 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.510-1490T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012911 | |||||||
| chr1:212013076 | C | T | 1 | a0001c0002t0005g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510-1655G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013076 | |||||||
| chr1:212013113 | T | A | 1 | a0001c0001t0002g0274 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.510-1692A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013113 | |||||||
| chr1:212013139 | C | T | 45 | a0001c0001t0001g0056 a0001c0001t0002g0281 a0001c0001t0003g0002 others(42): Show |
49 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.510-1718G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013139 | |||||||
| chr1:212013168 | T | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-1747A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013168 | |||||||
| chr1:212013320 | T | C | 1 | a0001c0001t0004g0009 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.510-1899A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013320 | |||||||
| chr1:212013332 | T | A | 1 | a0001c0001t0001g0160 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510-1911A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013332 | |||||||
| chr1:212013492 | T | G | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.510-2071A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013492 | |||||||
| chr1:212013782 | C | T | 84 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(81): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.510-2361G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013782 | |||||||
| chr1:212013788 | G | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-2367C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013788 | |||||||
| chr1:212013791 | C | G | 1 | a0001c0001t0002g0216 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.510-2370G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013791 | |||||||
| chr1:212013822 | C | T | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.510-2401G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013822 | |||||||
| chr1:212013864 | T | C | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.510-2443A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013864 | |||||||
| chr1:212013880 | T | C | 1 | a0001c0001t0003g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.510-2459A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013880 | |||||||
| chr1:212013986 | C | A | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.510-2565G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013986 | |||||||
| chr1:212014020 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.510-2599T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014020 | |||||||
| chr1:212014167 | T | TAAGAATA others(317): Show |
1 | a0002c0003t0007g0317 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.509+2718_509+2719i others(326): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014167 | |||||||
| chr1:212014167 | T | TAAGAATA others(318): Show |
1 | a0002c0003t0007g0316 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.509+2718_509+2719i others(327): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014167 | |||||||
| chr1:212014167 | T | TAAGAATA others(329): Show |
1 | a0002c0003t0020g0318 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.509+2718_509+2719i others(338): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014167 | |||||||
| chr1:212014167 | T | TAAGAATA others(330): Show |
1 | a0002c0007t0021g0319 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.509+2718_509+2719i others(339): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014167 | |||||||
| chr1:212014251 | G | A | 3 | a0001c0001t0003g0278 a0001c0001t0003g0279 a0001c0001t0003g0280 |
3 | HG00738.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.509+2635C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014251 | |||||||
| chr1:212014465 | C | CA | 75 | a0001c0001t0001g0038 a0001c0001t0001g0108 a0001c0001t0001g0109 others(72): Show |
89 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.509+2420dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014465 | |||||||
| chr1:212014465 | C | CAA | 13 | a0001c0001t0002g0173 a0001c0001t0002g0174 a0001c0001t0002g0192 others(10): Show |
13 | HG01109.hp2 HG02027.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.509+2419_509+2420d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014465 | |||||||
| chr1:212014597 | C | T | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509+2289G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014597 | |||||||
| chr1:212014598 | G | C | 16 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.509+2288C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014598 | |||||||
| chr1:212014671 | A | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+2215T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014671 | |||||||
| chr1:212014690 | T | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+2196A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014690 | |||||||
| chr1:212014718 | A | AT | 84 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(81): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.509+2167dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014718 | |||||||
| chr1:212014915 | T | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+1971A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014915 | |||||||
| chr1:212014954 | A | AC | 7 | a0001c0001t0001g0064 a0001c0001t0001g0113 a0001c0001t0003g0266 others(4): Show |
7 | HG02055.hp1 HG02523.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+1931dupG | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014954 | |||||||
| chr1:212014964 | G | A | 1 | a0001c0001t0003g0309 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.509+1922C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014964 | |||||||
| chr1:212014982 | T | TA | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+1903dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014982 | |||||||
| chr1:212015018 | C | A | 1 | a0001c0001t0003g0264 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.509+1868G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015018 | |||||||
| chr1:212015031 | G | A | 2 | a0001c0001t0003g0259 a0001c0001t0003g0260 |
2 | HG01243.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.509+1855C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015031 | |||||||
| chr1:212015063 | CGGCAGCC others(35): Show |
C | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+1781_509+1822d others(44): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015063 | |||||||
| chr1:212015090 | G | A | 1 | a0001c0004t0022g0322 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.509+1796C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015090 | |||||||
| chr1:212015098 | C | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+1788G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015098 | |||||||
| chr1:212015101 | G | A | 45 | a0001c0001t0001g0056 a0001c0001t0002g0281 a0001c0001t0003g0002 others(42): Show |
49 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.509+1785C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015101 | |||||||
| chr1:212015104 | CG | C | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+1781delC | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015104 | |||||||
| chr1:212015105 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.509+1781C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015105 | |||||||
| chr1:212015112 | C | T | 2 | a0002c0003t0020g0318 a0002c0007t0021g0319 |
2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.509+1774G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015112 | |||||||
| chr1:212015118 | G | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+1768C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015118 | |||||||
| chr1:212015150 | C | A | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.509+1736G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015150 | |||||||
| chr1:212015191 | A | AC | 20 | a0001c0001t0001g0062 a0001c0001t0001g0113 a0001c0001t0001g0114 others(17): Show |
20 | HG00597.hp1 HG01175.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.509+1694dupG | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015191 | |||||||
| chr1:212015195 | C | G | 1 | a0001c0001t0004g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.509+1691G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015195 | |||||||
| chr1:212015268 | G | A | 2 | a0001c0001t0001g0160 a0006c0012t0001g0156 |
2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.509+1618C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015268 | |||||||
| chr1:212015304 | G | A | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.509+1582C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015304 | |||||||
| chr1:212015356 | G | C | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.509+1530C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015356 | |||||||
| chr1:212015511 | T | C | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+1375A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015511 | |||||||
| chr1:212015569 | A | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+1317T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015569 | |||||||
| chr1:212015646 | T | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0112 |
2 | NA18963.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.509+1240A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015646 | |||||||
| chr1:212015710 | TA | T | 34 | a0001c0001t0001g0055 a0001c0001t0001g0113 a0001c0001t0001g0114 others(31): Show |
34 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.509+1175delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | |||||||
| chr1:212015710 | TAA | T | 111 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
119 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.509+1174_509+1175d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | |||||||
| chr1:212015710 | TAAA | T | 24 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0058 others(21): Show |
30 | HG00558.hp1 HG00733.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.509+1173_509+1175d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | |||||||
| chr1:212015710 | TAAAA | T | 84 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(81): Show |
93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.509+1172_509+1175d others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | |||||||
| chr1:212015710 | TAAAAA | T | 14 | a0001c0001t0002g0174 a0001c0001t0002g0205 a0001c0001t0002g0213 others(11): Show |
14 | HG01168.hp2 HG02523.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.509+1171_509+1175d others(7): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | |||||||
| chr1:212015710 | TAAAAAA | T | 36 | a0001c0001t0001g0056 a0001c0001t0003g0002 a0001c0001t0003g0020 others(33): Show |
40 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.509+1170_509+1175d others(8): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | |||||||
| chr1:212015710 | TAAAAAAA others(6): Show |
T | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509+1163_509+1175d others(15): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | |||||||
| chr1:212015710 | TAAAAAAA others(7): Show |
T | 8 | a0001c0001t0009g0198 a0001c0004t0007g0320 a0001c0004t0007g0321 others(5): Show |
8 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.509+1162_509+1175d others(16): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | |||||||
| chr1:212015761 | C | CAAAA | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+1121_509+1124d others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015761 | |||||||
| chr1:212015894 | G | A | 4 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+992C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015894 | |||||||
| chr1:212016104 | A | G | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509+782T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016104 | |||||||
| chr1:212016139 | T | C | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+747A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016139 | |||||||
| chr1:212016187 | A | G | 1 | a0001c0001t0003g0309 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.509+699T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016187 | |||||||
| chr1:212016192 | T | C | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+694A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016192 | |||||||
| chr1:212016320 | G | C | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.509+566C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016320 | |||||||
| chr1:212016344 | G | A | 3 | a0001c0001t0011g0202 a0001c0001t0011g0204 a0001c0001t0019g0203 |
3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+542C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016344 | |||||||
| chr1:212016370 | T | C | 1 | a0001c0001t0006g0130 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.509+516A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016370 | |||||||
| chr1:212016774 | A | C | 171 | a0001c0001t0001g0056 a0001c0001t0002g0011 a0001c0001t0002g0012 others(168): Show |
190 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.509+112T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016774 | |||||||
| chr1:212017033 | C | G | 1 | a0001c0001t0002g0212 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.372-10G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017033 | |||||||
| chr1:212017052 | C | T | 1 | a0001c0001t0008g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.372-29G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017052 | |||||||
| chr1:212017200 | T | C | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.372-177A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017200 | |||||||
| chr1:212017503 | C | A | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.372-480G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017503 | |||||||
| chr1:212017546 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0157 others(5): Show |
10 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.372-523G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017546 | |||||||
| chr1:212017575 | A | G | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.372-552T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017575 | |||||||
| chr1:212017621 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.372-598T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017621 | |||||||
| chr1:212017675 | G | T | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.372-652C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017675 | |||||||
| chr1:212017793 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.372-770G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017793 | |||||||
| chr1:212018164 | G | A | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.372-1141C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018164 | |||||||
| chr1:212018199 | T | C | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.372-1176A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018199 | |||||||
| chr1:212018204 | C | G | 5 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0001c0001t0002g0244 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.372-1181G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018204 | |||||||
| chr1:212018354 | T | C | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.372-1331A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018354 | |||||||
| chr1:212018503 | T | TA | 316 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(313): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.372-1481dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018503 | |||||||
| chr1:212018649 | G | A | 203 | a0001c0001t0001g0136 a0001c0001t0002g0011 a0001c0001t0002g0012 others(200): Show |
222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.371+1473C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018649 | |||||||
| chr1:212018660 | C | T | 2 | a0001c0001t0001g0052 a0005c0009t0001g0053 |
2 | NA18941.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.371+1462G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018660 | |||||||
| chr1:212018675 | C | T | 169 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(166): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.371+1447G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018675 | |||||||
| chr1:212018695 | C | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.371+1427G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018695 | |||||||
| chr1:212018729 | A | G | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.371+1393T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018729 | |||||||
| chr1:212018775 | T | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.371+1347A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018775 | |||||||
| chr1:212018779 | A | G | 5 | a0001c0001t0002g0209 a0001c0001t0002g0243 a0001c0001t0002g0244 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.371+1343T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018779 | |||||||
| chr1:212018917 | T | C | 11 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0166 others(8): Show |
11 | HG01433.hp1 HG02698.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.371+1205A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018917 | |||||||
| chr1:212019020 | C | T | 5 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0001t0004g0050 others(2): Show |
5 | HG01884.hp1 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.371+1102G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019020 | |||||||
| chr1:212019036 | G | A | 1 | a0001c0001t0002g0194 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.371+1086C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019036 | |||||||
| chr1:212019181 | A | G | 185 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(182): Show |
204 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.371+941T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019181 | |||||||
| chr1:212019250 | C | CAATA | 44 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(41): Show |
48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.371+868_371+871dup others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019250 | |||||||
| chr1:212019262 | T | A | 119 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(116): Show |
134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.371+860A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019262 | |||||||
| chr1:212019266 | T | A | 1 | a0001c0001t0002g0269 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.371+856A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019266 | |||||||
| chr1:212019421 | A | G | 10 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.371+701T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019421 | |||||||
| chr1:212019483 | G | A | 2 | a0001c0001t0003g0265 a0001c0001t0003g0266 |
2 | HG00621.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.371+639C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019483 | |||||||
| chr1:212019632 | T | G | 3 | a0001c0001t0011g0202 a0001c0001t0011g0204 a0001c0001t0019g0203 |
3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.371+490A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019632 | |||||||
| chr1:212019640 | A | G | 1 | a0002c0003t0007g0316 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.371+482T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019640 | |||||||
| chr1:212020011 | A | T | 2 | a0001c0001t0004g0048 a0001c0001t0004g0150 |
2 | HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.371+111T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212020011 | |||||||
| chr1:212020041 | A | G | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG02698.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.371+81T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212020041 | |||||||
| chr1:212020112 | C | T | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.371+10G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212020112 | |||||||
| chr1:212020817 | G | A | 3 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0037 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.224+266C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 2/19 | chr1 | 212020817 | |||||||
| chr1:212020848 | G | A | 16 | a0001c0001t0003g0017 a0001c0001t0003g0200 a0001c0001t0005g0001 others(13): Show |
23 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.224+235C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 2/19 | chr1 | 212020848 | |||||||
| chr1:212021003 | G | A | 1 | a0001c0004t0007g0321 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.224+80C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 2/19 | chr1 | 212021003 | |||||||
| chr1:212021219 | A | G | 1 | a0001c0001t0016g0313 | 1 | HG03453.hp2 | splice_region_variant&intron_variant | LOW | c.95-7T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021219 | |||||||
| chr1:212021278 | T | G | 2 | a0002c0003t0007g0316 a0002c0003t0007g0317 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.95-66A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021278 | |||||||
| chr1:212021373 | T | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-161A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021373 | |||||||
| chr1:212021387 | T | C | 30 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(27): Show |
34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.95-175A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021387 | |||||||
| chr1:212021395 | G | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-183C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021395 | |||||||
| chr1:212021463 | T | C | 30 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(27): Show |
34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.95-251A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021463 | |||||||
| chr1:212021620 | G | C | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.95-408C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021620 | |||||||
| chr1:212021628 | T | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA19057.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.95-416A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021628 | |||||||
| chr1:212021680 | T | TA | 26 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0002g0205 others(23): Show |
33 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.95-469dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021680 | |||||||
| chr1:212021680 | TA | T | 8 | a0001c0001t0001g0044 a0001c0001t0001g0144 a0001c0001t0002g0210 others(5): Show |
8 | HG00423.hp2 HG01255.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-469delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021680 | |||||||
| chr1:212021766 | T | G | 4 | a0001c0001t0003g0309 a0001c0001t0003g0310 a0001c0001t0003g0311 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-554A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021766 | |||||||
| chr1:212021855 | A | T | 1 | a0004c0011t0001g0043 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.95-643T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021855 | |||||||
| chr1:212021856 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.95-644A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021856 | |||||||
| chr1:212021889 | C | G | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.95-677G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021889 | |||||||
| chr1:212021948 | G | A | 3 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 |
3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.95-736C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021948 | |||||||
| chr1:212022002 | C | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-790G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212022002 | |||||||
| chr1:212022522 | TA | T | 44 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(41): Show |
48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.95-1311delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212022522 | |||||||
| chr1:212022670 | A | AATAT | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-1459_95-1458ins others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212022670 | |||||||
| chr1:212022829 | C | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-1617G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212022829 | |||||||
| chr1:212022869 | T | C | 84 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(81): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.95-1657A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212022869 | |||||||
| chr1:212023224 | G | C | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-2012C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023224 | |||||||
| chr1:212023260 | T | C | 2 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
2 | HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.95-2048A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023260 | |||||||
| chr1:212023535 | C | T | 1 | a0001c0001t0003g0254 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.95-2323G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023535 | |||||||
| chr1:212023588 | T | A | 4 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2376A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023588 | |||||||
| chr1:212023627 | ATAGACTC | A | 4 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0002g0247 others(1): Show |
4 | NA18941.hp1 NA18960.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2422_95-2416del others(7): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023627 | |||||||
| chr1:212023729 | A | G | 4 | a0001c0001t0002g0205 a0001c0001t0002g0206 a0001c0001t0002g0207 others(1): Show |
4 | HG03491.hp2 HG03492.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-2517T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023729 | |||||||
| chr1:212023842 | G | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-2630C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023842 | |||||||
| chr1:212023852 | T | A | 4 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2640A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023852 | |||||||
| chr1:212023876 | C | CTTTGA | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.95-2665_95-2664ins others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023876 | |||||||
| chr1:212023877 | C | CTTGAG | 7 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 others(4): Show |
7 | HG00642.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-2666_95-2665ins others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023877 | |||||||
| chr1:212023877 | C | G | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.95-2665G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023877 | |||||||
| chr1:212023987 | T | C | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-2775A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023987 | |||||||
| chr1:212024369 | A | T | 1 | a0001c0001t0008g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.95-3157T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024369 | |||||||
| chr1:212024411 | C | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-3199G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024411 | |||||||
| chr1:212024431 | T | C | 1 | a0001c0004t0022g0322 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.95-3219A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024431 | |||||||
| chr1:212024502 | A | G | 16 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.95-3290T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024502 | |||||||
| chr1:212024544 | C | T | 2 | a0002c0003t0007g0316 a0002c0003t0007g0317 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.95-3332G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024544 | |||||||
| chr1:212024772 | T | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-3560A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024772 | |||||||
| chr1:212024866 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.95-3654A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024866 | |||||||
| chr1:212024976 | G | T | 1 | a0001c0002t0009g0033 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.95-3764C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024976 | |||||||
| chr1:212025031 | G | T | 1 | a0001c0001t0003g0275 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.95-3819C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025031 | |||||||
| chr1:212025055 | G | A | 3 | a0001c0001t0003g0002 a0001c0001t0003g0306 a0001c0001t0018g0305 |
6 | HG00733.hp1 HG01074.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-3843C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025055 | |||||||
| chr1:212025086 | T | A | 4 | a0001c0002t0005g0003 a0001c0002t0005g0028 a0001c0002t0005g0029 others(1): Show |
6 | HG02922.hp1 HG03225.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-3874A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025086 | |||||||
| chr1:212025100 | T | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-3888A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025100 | |||||||
| chr1:212025278 | A | G | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4066T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025278 | |||||||
| chr1:212025294 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.95-4082C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025294 | |||||||
| chr1:212025344 | T | C | 1 | a0001c0001t0002g0249 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.95-4132A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025344 | |||||||
| chr1:212025484 | T | TA | 9 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0004t0007g0320 others(6): Show |
9 | HG00323.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-4273dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025484 | |||||||
| chr1:212025501 | C | G | 1 | a0001c0001t0002g0281 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.95-4289G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025501 | |||||||
| chr1:212025515 | T | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-4303A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025515 | |||||||
| chr1:212025537 | T | C | 16 | a0001c0001t0003g0163 a0001c0001t0003g0254 a0001c0001t0003g0255 others(13): Show |
16 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-4325A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025537 | |||||||
| chr1:212025614 | G | C | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4402C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025614 | |||||||
| chr1:212025659 | T | C | 1 | a0001c0001t0003g0307 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.95-4447A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025659 | |||||||
| chr1:212025690 | G | GA | 137 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(134): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.95-4479dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025690 | |||||||
| chr1:212025705 | AT | A | 3 | a0001c0001t0003g0197 a0001c0001t0003g0252 a0001c0001t0003g0253 |
3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.95-4494delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025705 | |||||||
| chr1:212025716 | A | G | 2 | a0001c0001t0003g0017 a0001c0001t0003g0200 |
3 | HG01069.hp1 HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.95-4504T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025716 | |||||||
| chr1:212025740 | C | T | 5 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0173 others(2): Show |
5 | NA18948.hp1 NA19002.hp1 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-4528G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025740 | |||||||
| chr1:212025799 | T | C | 3 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 |
3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.95-4587A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025799 | |||||||
| chr1:212025855 | T | TA | 30 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(27): Show |
34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.95-4644dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025855 | |||||||
| chr1:212025882 | A | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-4670T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025882 | |||||||
| chr1:212025965 | G | A | 4 | a0002c0003t0007g0316 a0002c0003t0007g0317 a0002c0003t0020g0318 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-4753C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025965 | |||||||
| chr1:212025966 | G | C | 1 | a0001c0001t0004g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.95-4754C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025966 | |||||||
| chr1:212026020 | G | A | 1 | a0001c0010t0002g0250 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.95-4808C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212026020 | |||||||
| chr1:212026073 | C | T | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.95-4861G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212026073 | |||||||
| chr1:212026269 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.95-5057A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212026269 | |||||||
| chr1:212026577 | A | AAAGG | 169 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(166): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.95-5366_95-5365ins others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212026577 | |||||||
| chr1:212026644 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.95-5432T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212026644 | |||||||
| chr1:212026703 | G | A | 1 | a0001c0001t0002g0196 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.95-5491C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212026703 | |||||||
| chr1:212027007 | A | C | 1 | a0001c0001t0002g0199 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.95-5795T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027007 | |||||||
| chr1:212027028 | A | G | 10 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-5816T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027028 | |||||||
| chr1:212027086 | C | A | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.95-5874G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027086 | |||||||
| chr1:212027130 | G | A | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-5918C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027130 | |||||||
| chr1:212027223 | G | T | 5 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-6011C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027223 | |||||||
| chr1:212027352 | A | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-6140T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027352 | |||||||
| chr1:212027397 | C | T | 1 | a0001c0001t0006g0041 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.95-6185G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027397 | |||||||
| chr1:212027400 | T | A | 2 | a0002c0003t0020g0318 a0002c0007t0021g0319 |
2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.95-6188A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027400 | |||||||
| chr1:212027659 | G | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-6447C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027659 | |||||||
| chr1:212027833 | C | CT | 166 | a0001c0001t0001g0040 a0001c0001t0002g0011 a0001c0001t0002g0012 others(163): Show |
185 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.95-6622dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027833 | |||||||
| chr1:212027913 | G | A | 1 | a0001c0001t0002g0267 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.95-6701C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027913 | |||||||
| chr1:212027961 | G | C | 1 | a0001c0001t0002g0268 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.95-6749C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027961 | |||||||
| chr1:212028073 | C | T | 2 | a0002c0003t0007g0316 a0002c0003t0007g0317 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.95-6861G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028073 | |||||||
| chr1:212028135 | G | T | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-6923C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028135 | |||||||
| chr1:212028172 | T | C | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.95-6960A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028172 | |||||||
| chr1:212028269 | A | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-7057T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028269 | |||||||
| chr1:212028276 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.95-7064C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028276 | |||||||
| chr1:212028389 | A | C | 44 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(41): Show |
48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.94+6955T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028389 | |||||||
| chr1:212028396 | T | C | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+6948A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028396 | |||||||
| chr1:212028450 | A | G | 10 | a0001c0001t0009g0198 a0001c0002t0009g0033 a0001c0002t0009g0034 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+6894T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028450 | |||||||
| chr1:212028541 | A | T | 1 | a0001c0001t0009g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.94+6803T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028541 | |||||||
| chr1:212028774 | G | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+6570C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028774 | |||||||
| chr1:212028858 | A | G | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+6486T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028858 | |||||||
| chr1:212029015 | G | A | 44 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(41): Show |
48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.94+6329C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212029015 | |||||||
| chr1:212029118 | C | T | 1 | a0001c0001t0003g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.94+6226G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212029118 | |||||||
| chr1:212029122 | A | T | 1 | a0001c0001t0001g0039 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.94+6222T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212029122 | |||||||
| chr1:212029144 | A | C | 2 | a0001c0004t0007g0320 a0001c0004t0007g0321 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.94+6200T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212029144 | |||||||
| chr1:212029340 | C | T | 34 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(31): Show |
40 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.94+6004G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212029340 | |||||||
| chr1:212029631 | T | A | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.94+5713A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212029631 | |||||||
| chr1:212029717 | T | C | 1 | a0001c0001t0004g0152 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94+5627A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212029717 | |||||||
| chr1:212030176 | C | T | 30 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(27): Show |
34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.94+5168G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030176 | |||||||
| chr1:212030293 | G | GT | 51 | a0001c0001t0001g0038 a0001c0001t0002g0281 a0001c0001t0003g0002 others(48): Show |
55 | HG00423.hp2 HG00597.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.94+5050dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030293 | |||||||
| chr1:212030293 | GT | G | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+5050delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030293 | |||||||
| chr1:212030294 | T | G | 1 | a0001c0001t0002g0269 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.94+5050A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030294 | |||||||
| chr1:212030552 | G | C | 1 | a0001c0001t0013g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.94+4792C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030552 | |||||||
| chr1:212030567 | G | A | 2 | a0001c0001t0003g0271 a0001c0001t0003g0272 |
2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.94+4777C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030567 | |||||||
| chr1:212030889 | C | T | 322 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.94+4455G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030889 | |||||||
| chr1:212030995 | AT | A | 3 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0037 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+4348delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030995 | |||||||
| chr1:212031101 | C | T | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+4243G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212031101 | |||||||
| chr1:212031450 | T | C | 1 | a0001c0001t0003g0273 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.94+3894A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212031450 | |||||||
| chr1:212031885 | T | C | 1 | a0001c0001t0002g0274 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.94+3459A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212031885 | |||||||
| chr1:212032194 | T | A | 3 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0037 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3150A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032194 | |||||||
| chr1:212032195 | C | A | 3 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0037 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3149G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032195 | |||||||
| chr1:212032196 | T | TGGA | 3 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0037 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3147_94+3148ins others(3): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032196 | |||||||
| chr1:212032197 | C | T | 3 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0037 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3147G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032197 | |||||||
| chr1:212032199 | G | T | 3 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0037 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3145C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032199 | |||||||
| chr1:212032200 | C | A | 3 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0037 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3144G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032200 | |||||||
| chr1:212032201 | A | C | 3 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0037 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3143T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032201 | |||||||
| chr1:212032202 | C | T | 3 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0008g0037 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3142G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032202 | |||||||
| chr1:212032236 | A | C | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.94+3108T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032236 | |||||||
| chr1:212032319 | G | C | 2 | a0002c0003t0020g0318 a0002c0007t0021g0319 |
2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.94+3025C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032319 | |||||||
| chr1:212032364 | G | C | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG02698.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.94+2980C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032364 | |||||||
| chr1:212032520 | A | G | 2 | a0002c0003t0020g0318 a0002c0007t0021g0319 |
2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.94+2824T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032520 | |||||||
| chr1:212032610 | G | A | 2 | a0002c0003t0007g0316 a0002c0003t0007g0317 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+2734C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032610 | |||||||
| chr1:212032634 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.94+2710C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032634 | |||||||
| chr1:212032700 | C | T | 2 | a0002c0003t0007g0316 a0002c0003t0007g0317 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+2644G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032700 | |||||||
| chr1:212032715 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.94+2629C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032715 | |||||||
| chr1:212032746 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.94+2598C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032746 | |||||||
| chr1:212032759 | G | A | 5 | a0001c0001t0003g0278 a0001c0001t0003g0279 a0001c0001t0003g0280 others(2): Show |
5 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+2585C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032759 | |||||||
| chr1:212032959 | T | G | 1 | a0001c0001t0006g0155 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.94+2385A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032959 | |||||||
| chr1:212033063 | G | A | 6 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(3): Show |
6 | HG02622.hp1 HG02886.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+2281C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033063 | |||||||
| chr1:212033078 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.94+2266A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033078 | |||||||
| chr1:212033111 | C | T | 3 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 |
3 | HG01069.hp2 HG01071.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.94+2233G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033111 | |||||||
| chr1:212033463 | T | G | 2 | a0002c0003t0007g0316 a0002c0003t0007g0317 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+1881A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033463 | |||||||
| chr1:212033496 | T | C | 185 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(182): Show |
204 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.94+1848A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033496 | |||||||
| chr1:212033548 | T | G | 30 | a0001c0001t0002g0281 a0001c0001t0003g0002 a0001c0001t0003g0020 others(27): Show |
34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.94+1796A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033548 | |||||||
| chr1:212033830 | C | A | 6 | a0001c0001t0003g0021 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+1514G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033830 | |||||||
| chr1:212033922 | A | C | 2 | a0001c0002t0009g0033 a0001c0002t0009g0034 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.94+1422T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033922 | |||||||
| chr1:212033990 | G | A | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1354C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033990 | |||||||
| chr1:212034143 | C | A | 2 | a0002c0003t0007g0316 a0002c0003t0007g0317 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+1201G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034143 | |||||||
| chr1:212034173 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1171T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034173 | |||||||
| chr1:212034174 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1170T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034174 | |||||||
| chr1:212034175 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1169G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034175 | |||||||
| chr1:212034177 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1167A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034177 | |||||||
| chr1:212034178 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1166T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034178 | |||||||
| chr1:212034179 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1165T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034179 | |||||||
| chr1:212034180 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1164A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034180 | |||||||
| chr1:212034181 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1163A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034181 | |||||||
| chr1:212034182 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1162A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034182 | |||||||
| chr1:212034183 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1161A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034183 | |||||||
| chr1:212034184 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1160G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034184 | |||||||
| chr1:212034185 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1159A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034185 | |||||||
| chr1:212034186 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1158A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034186 | |||||||
| chr1:212034189 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1155A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034189 | |||||||
| chr1:212034190 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1154A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034190 | |||||||
| chr1:212034192 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1152T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034192 | |||||||
| chr1:212034193 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1151A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034193 | |||||||
| chr1:212034199 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1145A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034199 | |||||||
| chr1:212034201 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1143G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034201 | |||||||
| chr1:212034203 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1141G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034203 | |||||||
| chr1:212034204 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1140A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034204 | |||||||
| chr1:212034205 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1139T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034205 | |||||||
| chr1:212034209 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1135T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034209 | |||||||
| chr1:212034212 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1132G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034212 | |||||||
| chr1:212034213 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1131A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034213 | |||||||
| chr1:212034217 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1127T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034217 | |||||||
| chr1:212034218 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1126G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034218 | |||||||
| chr1:212034219 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1125A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034219 | |||||||
| chr1:212034220 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1124G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034220 | |||||||
| chr1:212034221 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1123T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034221 | |||||||
| chr1:212034222 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1122T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034222 | |||||||
| chr1:212034223 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1121G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034223 | |||||||
| chr1:212034224 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1120G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034224 | |||||||
| chr1:212034226 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1118T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034226 | |||||||
| chr1:212034227 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1117T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034227 | |||||||
| chr1:212034230 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1114T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034230 | |||||||
| chr1:212034232 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1112A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034232 | |||||||
| chr1:212034233 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1111T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034233 | |||||||
| chr1:212034234 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1110A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034234 | |||||||
| chr1:212034235 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1109G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034235 | |||||||
| chr1:212034236 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1108G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034236 | |||||||
| chr1:212034237 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1107G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034237 | |||||||
| chr1:212034239 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1105A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034239 | |||||||
| chr1:212034240 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1104A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034240 | |||||||
| chr1:212034241 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1103T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034241 | |||||||
| chr1:212034279 | A | G | 1 | a0001c0001t0003g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.94+1065T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034279 | |||||||
| chr1:212034725 | G | A | 2 | a0001c0001t0004g0314 a0001c0001t0004g0315 |
2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.94+619C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034725 | |||||||
| chr1:212034793 | C | CT | 7 | a0001c0004t0007g0320 a0001c0004t0007g0321 a0001c0004t0022g0322 others(4): Show |
7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+550dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034793 | |||||||
| chr1:212034882 | C | T | 1 | a0001c0001t0002g0031 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.94+462G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034882 | |||||||
| chr1:212034986 | C | G | 11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0023 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+358G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034986 | |||||||
| chr1:212035051 | A | G | 2 | a0002c0003t0007g0316 a0002c0003t0007g0317 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+293T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212035051 | |||||||
| chr1:212035114 | A | C | 1 | a0001c0001t0003g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.94+230T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212035114 |