Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6767 |
| ensemblid | ENSG00000100380.15 |
| hgncid | 11343 |
| symbol | ST13 |
| name | ST13 Hsp70 interacting protein |
| refseq_nuc | NM_003932.5 |
| refseq_prot | NP_003923.2 |
| ensembl_nuc | ENST00000216218.8 |
| ensembl_prot | ENSP00000216218.3 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 40824535 |
| end | 40856639 |
| strand | - |
| ver | v1.2 |
| region | chr22:40824535-40856639 |
| region5000 | chr22:40819535-40861639 |
| regionname0 | ST13_chr22_40824535_40856639 |
| regionname5000 | ST13_chr22_40819535_40861639 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 369 | 328 | 82 | 49 | 143 | 15 | 37 | 108 | ST13_chr22_40819535_40861639 | ST13 | MDPRK others(364): Show |
chr22 | 40819535 | 40861639 |
| a0002 | 0/0 | 369 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | MDPRK others(364): Show |
chr22 | 40819535 | 40861639 |
| a0003 | 0/0 | 369 | 7 | 0 | 3 | 0 | 1 | 3 | 0 | ST13_chr22_40819535_40861639 | ST13 | MDPRK others(364): Show |
chr22 | 40819535 | 40861639 |
| a0004 | 0/0 | 369 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | MDPRK others(364): Show |
chr22 | 40819535 | 40861639 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1107 | 328 | 82 | 49 | 143 | 15 | 37 | ST13_chr22_40819535_40861639 | ST13 | ATGGA others(1102): Show |
chr22 | 40819535 | 40861639 | ||
| a0002c0002 | 0/0 | 1107 | 8 | 8 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | ATGGA others(1102): Show |
chr22 | 40819535 | 40861639 | ||
| a0003c0003 | 0/0 | 1107 | 7 | 0 | 3 | 0 | 1 | 3 | ST13_chr22_40819535_40861639 | ST13 | ATGGA others(1102): Show |
chr22 | 40819535 | 40861639 | ||
| a0004c0004 | 0/0 | 1107 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | ATGGA others(1102): Show |
chr22 | 40819535 | 40861639 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3212 | 261 | 66 | 44 | 98 | 14 | 37 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0001c0001t0002 | 0/0 | 3212 | 30 | 0 | 0 | 30 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0001c0001t0003 | 0/0 | 3212 | 12 | 0 | 0 | 12 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0001c0001t0004 | 0/0 | 3212 | 6 | 4 | 2 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0001c0001t0005 | 0/0 | 3212 | 4 | 3 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0001c0001t0006 | 0/0 | 3212 | 2 | 2 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0001c0001t0007 | 0/0 | 3212 | 2 | 1 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0001c0001t0008 | 0/0 | 3212 | 2 | 2 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0001c0001t0009 | 0/0 | 3212 | 2 | 1 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0001c0001t0010 | 0/0 | 3212 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0001c0001t0011 | 0/0 | 3212 | 1 | 0 | 0 | 0 | 1 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0001c0001t0012 | 0/0 | 3212 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0001c0001t0013 | 0/0 | 3212 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0001c0001t0014 | 0/0 | 3212 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0001c0001t0015 | 0/0 | 3212 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0002c0002t0001 | 0/0 | 3212 | 8 | 8 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0003c0003t0001 | 0/0 | 3212 | 7 | 0 | 3 | 0 | 1 | 3 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| a0004c0004t0001 | 0/0 | 3212 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | CTTGC others(3207): Show |
chr22 | 40819535 | 40861639 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 0 | 1 | 13 | 2 | 6 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0002 | 0/0 | 21 | 5 | 2 | 13 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0003 | 0/0 | 18 | 4 | 10 | 0 | 1 | 3 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0055 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0148 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0001g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0002g0004 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0003g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0003g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0003g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0004g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0005g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0006g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0007g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0009g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0010g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0011g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0012g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0013g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0014g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0001c0001t0015g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0002c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0002c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0003c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0003c0003t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0003c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0003c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| a0004c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | GBR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | GBR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | GBR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0031 | EUR | GBR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00558 | hp1 | a0004 | c0004 | t0001 | g0126 | EAS | CHS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00639 | hp2 | a0001 | c0001 | t0009 | g0030 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0101 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0032 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0102 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0042 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0088 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | CLM | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0029 | AMR | PEL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CDX | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0187 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0087 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0195 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02630 | hp2 | a0001 | c0001 | t0013 | g0070 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0062 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02886 | hp2 | a0001 | c0001 | t0012 | g0060 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | ESN | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0189 | AFR | ESN | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0061 | AFR | MSL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03098 | hp2 | a0001 | c0001 | t0015 | g0197 | AFR | MSL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | ESN | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0064 | AFR | MSL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0042 | AFR | MSL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03490 | hp1 | a0003 | c0003 | t0001 | g0031 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0063 | AFR | MSL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03831 | hp1 | a0003 | c0003 | t0001 | g0032 | SAS | BEB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0100 | SAS | BEB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | STU | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0030 | AFR | YRI | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0122 | AFR | YRI | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0188 | AFR | YRI | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18952 | hp1 | a0001 | c0001 | t0010 | g0050 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18969 | hp1 | a0001 | c0001 | t0010 | g0050 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19090 | hp1 | a0001 | c0001 | t0014 | g0173 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA20752 | hp2 | a0001 | c0001 | t0011 | g0157 | EUR | TSI | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | GIH | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | USA | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | USA | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | USA | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0196 | REF | REF | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0148 | REF | REF | ST13_chr22_40819535_40861639 | ST13 | chr22 | 40819535 | 40861639 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40826539 | T | G | 1 | a0001 | 1 | HG03098.hp2 | stop_lost | HIGH | c.1109A>C | p.Ter370Serext*? | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 12/12 | 1208/3212 | 1109/1110 | 370/369 | chr22 | 40826539 | |||
| chr22:40827186 | C | T | 1 | a0003 | 7 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
missense_variant | MODERATE | c.891G>A | p.Met297Ile | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 11/12 | 990/3212 | 891/1110 | 297/369 | chr22 | 40827186 | |||
| chr22:40827202 | T | C | 1 | a0002 | 8 | HG02258.hp2 HG02615.hp1 HG02717.hp1 others(5): Show |
missense_variant | MODERATE | c.875A>G | p.Asn292Ser | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 11/12 | 974/3212 | 875/1110 | 292/369 | chr22 | 40827202 | |||
| chr22:40840692 | T | C | 1 | a0004 | 1 | HG00558.hp1 | missense_variant&splice_region_variant | MODERATE | c.316A>G | p.Ile106Val | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/12 | 415/3212 | 316/1110 | 106/369 | chr22 | 40840692 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40824584 | C | G | 1 | a0001c0001t0005 | 4 | HG01934.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1954G>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 12/12 | 1954 | chr22 | 40824584 | ||||||
| chr22:40824752 | A | G | 2 | a0001c0001t0002 a0001c0001t0004 |
36 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1786T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 12/12 | 1786 | chr22 | 40824752 | ||||||
| chr22:40825179 | A | C | 1 | a0001c0001t0013 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1359T>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 12/12 | 1359 | chr22 | 40825179 | ||||||
| chr22:40825287 | C | A | 1 | a0001c0001t0014 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1251G>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 12/12 | 1251 | chr22 | 40825287 | ||||||
| chr22:40825314 | A | G | 2 | a0001c0001t0006 a0001c0001t0012 |
3 | HG02886.hp2 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1224T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 12/12 | 1224 | chr22 | 40825314 | ||||||
| chr22:40825428 | A | G | 1 | a0001c0001t0011 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1110T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 12/12 | 1110 | chr22 | 40825428 | ||||||
| chr22:40825764 | T | C | 1 | a0001c0001t0002 | 30 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*774A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 12/12 | 774 | chr22 | 40825764 | ||||||
| chr22:40825887 | C | A | 1 | a0001c0001t0007 | 2 | HG01109.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*651G>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 12/12 | 651 | chr22 | 40825887 | ||||||
| chr22:40825889 | C | T | 1 | a0001c0001t0006 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*649G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 12/12 | 649 | chr22 | 40825889 | ||||||
| chr22:40825964 | G | C | 2 | a0001c0001t0005 a0001c0001t0008 |
6 | HG01934.hp2 HG02809.hp1 HG03098.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*574C>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 12/12 | 574 | chr22 | 40825964 | ||||||
| chr22:40826475 | G | A | 1 | a0001c0001t0009 | 2 | HG00639.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*63C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 12/12 | 63 | chr22 | 40826475 | ||||||
| chr22:40826523 | T | C | 1 | a0001c0001t0010 | 2 | NA18952.hp1 NA18969.hp1 |
3_prime_UTR_variant | MODIFIER | c.*15A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 12/12 | 15 | chr22 | 40826523 | ||||||
| chr22:40856595 | G | C | 1 | a0001c0001t0003 | 12 | NA18949.hp2 NA18969.hp2 NA18975.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-55C>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/12 | 55 | chr22 | 40856595 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40826769 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0110 a0001c0001t0001g0114 others(1): Show |
7 | HG00423.hp2 HG00735.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.982-103C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 11/11 | chr22 | 40826769 | |||||||
| chr22:40826900 | G | GCTA | 50 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(47): Show |
76 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.981+193_981+195dup others(3): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 11/11 | chr22 | 40826900 | |||||||
| chr22:40827243 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0002g0078 |
2 | HG00423.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.848-14A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40827243 | |||||||
| chr22:40827678 | AAT | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0009g0030 |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-451_848-450del others(2): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40827678 | |||||||
| chr22:40827846 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.848-617C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40827846 | |||||||
| chr22:40827855 | G | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(47): Show |
76 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.848-626C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40827855 | |||||||
| chr22:40827897 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.848-668T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40827897 | |||||||
| chr22:40828015 | C | G | 13 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0190 others(10): Show |
18 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.848-786G>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40828015 | |||||||
| chr22:40828389 | G | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
96 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.848-1160C>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40828389 | |||||||
| chr22:40828448 | CA | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.847+1177delT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40828448 | |||||||
| chr22:40828448 | CAA | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0090 a0001c0001t0001g0093 others(3): Show |
9 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.847+1176_847+1177d others(4): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40828448 | |||||||
| chr22:40828591 | C | T | 5 | a0002c0002t0001g0017 a0002c0002t0001g0122 a0002c0002t0001g0188 others(2): Show |
7 | HG02615.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.847+1035G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40828591 | |||||||
| chr22:40828602 | G | C | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0009g0030 |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.847+1024C>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40828602 | |||||||
| chr22:40829396 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.847+230T>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40829396 | |||||||
| chr22:40829458 | T | A | 2 | a0001c0001t0006g0020 a0001c0001t0012g0060 |
3 | HG02886.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.847+168A>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40829458 | |||||||
| chr22:40829549 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.847+77T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40829549 | |||||||
| chr22:40829609 | C | T | 1 | a0001c0001t0002g0024 | 2 | HG00597.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.847+17G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 10/11 | chr22 | 40829609 | |||||||
| chr22:40829687 | AG | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0015g0197 |
3 | HG03098.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-14delC | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40829687 | |||||||
| chr22:40829705 | TAGA | T | 7 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(4): Show |
9 | HG01934.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.799-34_799-32delTC others(1): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40829705 | |||||||
| chr22:40829903 | AACAAGTA others(12): Show |
A | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-248_799-230del others(19): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40829903 | |||||||
| chr22:40829923 | A | C | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-249T>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40829923 | |||||||
| chr22:40829969 | A | T | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-295T>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40829969 | |||||||
| chr22:40829990 | G | T | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-316C>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40829990 | |||||||
| chr22:40830006 | C | A | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-332G>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830006 | |||||||
| chr22:40830008 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-334T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830008 | |||||||
| chr22:40830010 | C | A | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-336G>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830010 | |||||||
| chr22:40830011 | A | C | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-337T>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830011 | |||||||
| chr22:40830013 | G | GATCCAGT others(4): Show |
1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-340_799-339ins others(11): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830013 | |||||||
| chr22:40830025 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-351G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830025 | |||||||
| chr22:40830026 | T | G | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-352A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830026 | |||||||
| chr22:40830036 | T | A | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-362A>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830036 | |||||||
| chr22:40830037 | T | G | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-363A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830037 | |||||||
| chr22:40830047 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-373A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830047 | |||||||
| chr22:40830048 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-374G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830048 | |||||||
| chr22:40830049 | T | G | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-375A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830049 | |||||||
| chr22:40830064 | A | T | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-390T>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830064 | |||||||
| chr22:40830066 | T | G | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-392A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830066 | |||||||
| chr22:40830069 | A | T | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-395T>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830069 | |||||||
| chr22:40830070 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-396C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830070 | |||||||
| chr22:40830071 | A | T | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-397T>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830071 | |||||||
| chr22:40830098 | T | G | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-424A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830098 | |||||||
| chr22:40830320 | A | C | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.798+520T>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830320 | |||||||
| chr22:40830380 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0013g0070 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.798+460C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830380 | |||||||
| chr22:40830578 | T | C | 2 | a0001c0001t0008g0063 a0001c0001t0008g0064 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.798+262A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830578 | |||||||
| chr22:40830616 | CAA | C | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0009g0030 |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+222_798+223del others(2): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830616 | |||||||
| chr22:40830694 | A | T | 1 | a0001c0001t0001g0131 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.798+146T>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 9/11 | chr22 | 40830694 | |||||||
| chr22:40830964 | A | G | 1 | a0001c0001t0004g0085 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.682-8T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 8/11 | chr22 | 40830964 | |||||||
| chr22:40831082 | C | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.682-126G>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 8/11 | chr22 | 40831082 | |||||||
| chr22:40831342 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.682-386T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 8/11 | chr22 | 40831342 | |||||||
| chr22:40831381 | A | G | 5 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(2): Show |
6 | HG01934.hp2 HG02809.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-425T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 8/11 | chr22 | 40831381 | |||||||
| chr22:40831411 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.682-455C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 8/11 | chr22 | 40831411 | |||||||
| chr22:40831453 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0090 a0001c0001t0001g0091 others(7): Show |
13 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.682-497T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 8/11 | chr22 | 40831453 | |||||||
| chr22:40831592 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0117 |
3 | HG02602.hp1 HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.682-636T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 8/11 | chr22 | 40831592 | |||||||
| chr22:40832000 | G | A | 1 | a0002c0002t0001g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.681+569C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 8/11 | chr22 | 40832000 | |||||||
| chr22:40832267 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.681+302T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 8/11 | chr22 | 40832267 | |||||||
| chr22:40832521 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.681+48G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 8/11 | chr22 | 40832521 | |||||||
| chr22:40832688 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.579-17G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40832688 | |||||||
| chr22:40832804 | A | G | 5 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(2): Show |
6 | HG01934.hp2 HG02809.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.579-133T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40832804 | |||||||
| chr22:40832916 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.579-245A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40832916 | |||||||
| chr22:40832975 | G | A | 2 | a0001c0001t0006g0020 a0001c0001t0012g0060 |
3 | HG02886.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.579-304C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40832975 | |||||||
| chr22:40833145 | C | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(44): Show |
72 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.579-474G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40833145 | |||||||
| chr22:40833521 | C | T | 1 | a0001c0001t0005g0061 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.579-850G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40833521 | |||||||
| chr22:40833564 | CA | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.579-894delT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40833564 | |||||||
| chr22:40833740 | G | A | 2 | a0001c0001t0006g0020 a0001c0001t0012g0060 |
3 | HG02886.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.579-1069C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40833740 | |||||||
| chr22:40833999 | A | G | 2 | a0003c0003t0001g0101 a0003c0003t0001g0102 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.579-1328T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40833999 | |||||||
| chr22:40834234 | T | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(47): Show |
76 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.578+1326A>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40834234 | |||||||
| chr22:40834348 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.578+1212A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40834348 | |||||||
| chr22:40834501 | T | C | 7 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(4): Show |
9 | HG01934.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.578+1059A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40834501 | |||||||
| chr22:40834561 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.578+999T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40834561 | |||||||
| chr22:40834889 | T | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(13): Show |
21 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.578+671A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40834889 | |||||||
| chr22:40835049 | A | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
98 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.578+511T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40835049 | |||||||
| chr22:40835065 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.578+495G>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40835065 | |||||||
| chr22:40835069 | C | A | 1 | a0001c0001t0001g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.578+491G>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40835069 | |||||||
| chr22:40835432 | A | C | 1 | a0001c0001t0001g0175 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.578+128T>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 7/11 | chr22 | 40835432 | |||||||
| chr22:40836003 | A | G | 1 | a0001c0001t0006g0020 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.383-116T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40836003 | |||||||
| chr22:40836165 | AAGT | A | 7 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(4): Show |
9 | HG01934.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-281_383-279del others(3): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40836165 | |||||||
| chr22:40836294 | A | C | 24 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0081 others(21): Show |
42 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-407T>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40836294 | |||||||
| chr22:40836314 | G | C | 7 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(4): Show |
9 | HG01934.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-427C>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40836314 | |||||||
| chr22:40836314 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.383-427C>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40836314 | |||||||
| chr22:40836339 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.383-452G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40836339 | |||||||
| chr22:40836388 | T | C | 1 | a0003c0003t0001g0031 | 2 | HG00140.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.383-501A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40836388 | |||||||
| chr22:40836469 | AAAAAGT | A | 3 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 |
4 | HG01934.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-588_383-583del others(6): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40836469 | |||||||
| chr22:40836590 | T | C | 47 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(44): Show |
72 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.383-703A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40836590 | |||||||
| chr22:40836770 | T | TA | 4 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0083 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-884dupT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40836770 | |||||||
| chr22:40836809 | G | C | 1 | a0001c0001t0001g0145 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.383-922C>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40836809 | |||||||
| chr22:40836842 | A | AT | 7 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0190 others(4): Show |
10 | HG02055.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.383-956dupA | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40836842 | |||||||
| chr22:40836882 | G | C | 2 | a0001c0001t0006g0020 a0001c0001t0012g0060 |
3 | HG02886.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.383-995C>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40836882 | |||||||
| chr22:40837040 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.383-1153A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40837040 | |||||||
| chr22:40837179 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.383-1292C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40837179 | |||||||
| chr22:40837200 | A | C | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-1313T>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40837200 | |||||||
| chr22:40837292 | C | A | 1 | a0001c0001t0001g0007 | 4 | HG03130.hp1 HG03139.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-1405G>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40837292 | |||||||
| chr22:40837360 | A | C | 1 | a0001c0001t0001g0154 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.383-1473T>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40837360 | |||||||
| chr22:40837385 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0106 |
4 | HG00642.hp1 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-1498C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40837385 | |||||||
| chr22:40837406 | G | A | 1 | a0001c0001t0008g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.383-1519C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40837406 | |||||||
| chr22:40837412 | TCAAGACC others(24): Show |
T | 1 | a0001c0001t0001g0172 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.383-1556_383-1526d others(33): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40837412 | |||||||
| chr22:40837422 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.383-1535G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40837422 | |||||||
| chr22:40837475 | C | T | 24 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0081 others(21): Show |
42 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-1588G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40837475 | |||||||
| chr22:40837476 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.383-1589C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40837476 | |||||||
| chr22:40837586 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(13): Show |
21 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.383-1699G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40837586 | |||||||
| chr22:40837867 | T | C | 13 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0190 others(10): Show |
18 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.383-1980A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40837867 | |||||||
| chr22:40837899 | C | T | 1 | a0003c0003t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.383-2012G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40837899 | |||||||
| chr22:40838006 | GT | G | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0009g0030 |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-2120delA | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40838006 | |||||||
| chr22:40838063 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.383-2176G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40838063 | |||||||
| chr22:40838123 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.383-2236T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40838123 | |||||||
| chr22:40838179 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.383-2292C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40838179 | |||||||
| chr22:40838295 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.382+2331A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40838295 | |||||||
| chr22:40838327 | C | T | 7 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(4): Show |
9 | HG01934.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.382+2299G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40838327 | |||||||
| chr22:40838458 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0104 a0001c0001t0001g0138 |
4 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+2168C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40838458 | |||||||
| chr22:40838599 | C | CA | 17 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0054 others(14): Show |
23 | HG00140.hp1 HG02055.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.382+2026dupT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40838599 | |||||||
| chr22:40838599 | CA | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0069 a0001c0001t0001g0071 others(3): Show |
8 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.382+2026delT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40838599 | |||||||
| chr22:40838863 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.382+1763C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40838863 | |||||||
| chr22:40838911 | T | TA | 10 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0046 others(7): Show |
13 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.382+1714dupT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40838911 | |||||||
| chr22:40838911 | TA | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(79): Show |
130 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.382+1714delT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40838911 | |||||||
| chr22:40838911 | TAA | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
7 | HG00639.hp2 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.382+1713_382+1714d others(4): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40838911 | |||||||
| chr22:40838915 | A | T | 1 | a0001c0001t0001g0014 | 3 | NA18961.hp2 NA19058.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.382+1711T>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40838915 | |||||||
| chr22:40839094 | C | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0111 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.382+1532G>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839094 | |||||||
| chr22:40839107 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.382+1519T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839107 | |||||||
| chr22:40839259 | C | T | 5 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(2): Show |
6 | HG01934.hp2 HG02809.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+1367G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839259 | |||||||
| chr22:40839337 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.382+1289A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839337 | |||||||
| chr22:40839352 | T | C | 1 | a0001c0001t0009g0030 | 2 | HG00639.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.382+1274A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839352 | |||||||
| chr22:40839454 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.382+1172C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839454 | |||||||
| chr22:40839503 | G | A | 1 | a0001c0001t0008g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.382+1123C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839503 | |||||||
| chr22:40839548 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.382+1078G>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839548 | |||||||
| chr22:40839635 | C | T | 24 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0081 others(21): Show |
42 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.382+991G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839635 | |||||||
| chr22:40839669 | G | A | 1 | a0001c0001t0002g0077 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.382+957C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839669 | |||||||
| chr22:40839718 | C | T | 3 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 |
4 | HG01934.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+908G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839718 | |||||||
| chr22:40839740 | C | T | 8 | a0001c0001t0004g0086 a0001c0001t0005g0029 a0001c0001t0005g0061 others(5): Show |
10 | HG01934.hp2 HG02055.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.382+886G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839740 | |||||||
| chr22:40839742 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.382+884T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839742 | |||||||
| chr22:40839970 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.382+656C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839970 | |||||||
| chr22:40839993 | AC | A | 5 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(2): Show |
6 | HG01934.hp2 HG02809.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+632delG | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40839993 | |||||||
| chr22:40840075 | G | A | 1 | a0001c0001t0010g0050 | 2 | NA18952.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.382+551C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40840075 | |||||||
| chr22:40840187 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.382+439G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40840187 | |||||||
| chr22:40840326 | C | T | 1 | a0002c0002t0001g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.382+300G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40840326 | |||||||
| chr22:40840335 | C | CT | 29 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0084 others(26): Show |
47 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.382+290dupA | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40840335 | |||||||
| chr22:40840400 | G | A | 1 | a0001c0001t0009g0030 | 2 | HG00639.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.382+226C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 5/11 | chr22 | 40840400 | |||||||
| chr22:40840835 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.316-143A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40840835 | |||||||
| chr22:40840927 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.316-235G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40840927 | |||||||
| chr22:40841185 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0069 a0001c0001t0001g0071 others(2): Show |
7 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.316-493G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40841185 | |||||||
| chr22:40841203 | G | GA | 38 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0023 others(35): Show |
54 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.316-512dupT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40841203 | |||||||
| chr22:40841203 | GA | G | 5 | a0001c0001t0001g0073 a0001c0001t0001g0105 a0001c0001t0001g0132 others(2): Show |
6 | HG00323.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-512delT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40841203 | |||||||
| chr22:40841212 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.316-520T>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40841212 | |||||||
| chr22:40841285 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.316-593C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40841285 | |||||||
| chr22:40841561 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.316-869G>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40841561 | |||||||
| chr22:40841565 | G | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(12): Show |
20 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.316-873C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40841565 | |||||||
| chr22:40841761 | CT | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.316-1070delA | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40841761 | |||||||
| chr22:40841813 | G | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0111 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.316-1121C>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40841813 | |||||||
| chr22:40841853 | A | G | 5 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(2): Show |
6 | HG01934.hp2 HG02809.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.316-1161T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40841853 | |||||||
| chr22:40842065 | T | G | 1 | a0001c0001t0001g0008 | 4 | HG00408.hp2 HG00544.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.316-1373A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40842065 | |||||||
| chr22:40842108 | G | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0105 a0001c0001t0001g0121 others(5): Show |
9 | HG00323.hp2 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.316-1416C>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40842108 | |||||||
| chr22:40842159 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.316-1467T>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40842159 | |||||||
| chr22:40842379 | A | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0111 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.316-1687T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40842379 | |||||||
| chr22:40842437 | A | T | 1 | a0001c0001t0001g0171 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.316-1745T>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40842437 | |||||||
| chr22:40842918 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.315+1921T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40842918 | |||||||
| chr22:40843231 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.315+1608C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40843231 | |||||||
| chr22:40843517 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.315+1322A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40843517 | |||||||
| chr22:40843535 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.315+1304G>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40843535 | |||||||
| chr22:40843711 | T | C | 1 | a0001c0001t0001g0049 | 2 | NA18983.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.315+1128A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40843711 | |||||||
| chr22:40843776 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0144 |
3 | HG02027.hp1 NA18747.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.315+1063T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40843776 | |||||||
| chr22:40843810 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.315+1029C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40843810 | |||||||
| chr22:40843884 | A | AT | 9 | a0001c0001t0001g0174 a0001c0001t0001g0191 a0001c0001t0005g0029 others(6): Show |
11 | HG01934.hp2 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.315+954dupA | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40843884 | |||||||
| chr22:40843884 | AT | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(66): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.315+954delA | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40843884 | |||||||
| chr22:40843884 | ATT | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(8): Show |
16 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.315+953_315+954del others(2): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40843884 | |||||||
| chr22:40843922 | G | C | 1 | a0001c0001t0004g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.315+917C>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40843922 | |||||||
| chr22:40843941 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.315+898C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40843941 | |||||||
| chr22:40843977 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.315+862C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40843977 | |||||||
| chr22:40844163 | G | A | 5 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(2): Show |
6 | HG01934.hp2 HG02809.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.315+676C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40844163 | |||||||
| chr22:40844647 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.315+192T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40844647 | |||||||
| chr22:40844831 | G | A | 22 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(19): Show |
40 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(37): Show |
splice_region_variant&intron_variant | LOW | c.315+8C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 4/11 | chr22 | 40844831 | |||||||
| chr22:40844967 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.245-58G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40844967 | |||||||
| chr22:40845040 | T | C | 13 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0190 others(10): Show |
18 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.245-131A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40845040 | |||||||
| chr22:40845231 | A | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0111 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.245-322T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40845231 | |||||||
| chr22:40845331 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0069 a0001c0001t0001g0071 others(3): Show |
8 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.245-422T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40845331 | |||||||
| chr22:40845367 | T | G | 1 | a0001c0001t0001g0166 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.245-458A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40845367 | |||||||
| chr22:40845416 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.245-507G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40845416 | |||||||
| chr22:40845420 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.245-511G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40845420 | |||||||
| chr22:40845498 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.245-589G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40845498 | |||||||
| chr22:40845730 | T | TAC | 16 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(13): Show |
21 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.245-823_245-822dup others(2): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40845730 | |||||||
| chr22:40845730 | TAC | T | 13 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0190 others(10): Show |
18 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.245-823_245-822del others(2): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40845730 | |||||||
| chr22:40845941 | C | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(48): Show |
93 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.245-1032G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40845941 | |||||||
| chr22:40845984 | T | A | 18 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0025 others(15): Show |
36 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.245-1075A>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40845984 | |||||||
| chr22:40846013 | C | G | 6 | a0002c0002t0001g0017 a0002c0002t0001g0122 a0002c0002t0001g0187 others(3): Show |
8 | HG02258.hp2 HG02615.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.245-1104G>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40846013 | |||||||
| chr22:40846014 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0167 |
3 | HG01515.hp2 HG01517.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.245-1105C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40846014 | |||||||
| chr22:40846022 | T | C | 5 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
5 | HG00099.hp1 HG01433.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1113A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40846022 | |||||||
| chr22:40846179 | AC | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0069 a0001c0001t0001g0071 others(2): Show |
7 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-1271delG | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40846179 | |||||||
| chr22:40846285 | T | C | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0168 others(1): Show |
6 | HG00621.hp2 NA18747.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-1376A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40846285 | |||||||
| chr22:40846306 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.245-1397A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40846306 | |||||||
| chr22:40846308 | T | C | 1 | a0001c0001t0008g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.245-1399A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40846308 | |||||||
| chr22:40846311 | A | G | 2 | a0001c0001t0006g0020 a0001c0001t0012g0060 |
3 | HG02886.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.245-1402T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40846311 | |||||||
| chr22:40846391 | G | T | 1 | a0001c0001t0015g0197 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.245-1482C>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40846391 | |||||||
| chr22:40846533 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.245-1624T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40846533 | |||||||
| chr22:40846594 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.245-1685C>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40846594 | |||||||
| chr22:40846602 | G | C | 7 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(4): Show |
9 | HG01934.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+1692C>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40846602 | |||||||
| chr22:40846698 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.244+1596T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40846698 | |||||||
| chr22:40846699 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.244+1595A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40846699 | |||||||
| chr22:40847079 | A | G | 7 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(4): Show |
9 | HG01934.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+1215T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40847079 | |||||||
| chr22:40847085 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.244+1209C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40847085 | |||||||
| chr22:40847096 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.244+1198A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40847096 | |||||||
| chr22:40847168 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0106 |
4 | HG00642.hp1 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+1126T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40847168 | |||||||
| chr22:40847358 | A | G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(12): Show |
20 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.244+936T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40847358 | |||||||
| chr22:40847378 | C | CA | 46 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(43): Show |
73 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.244+915dupT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40847378 | |||||||
| chr22:40847528 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.244+766C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40847528 | |||||||
| chr22:40847548 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0005g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.244+734_244+745del others(12): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40847548 | |||||||
| chr22:40847548 | CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0001g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.244+728_244+745del others(18): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40847548 | |||||||
| chr22:40847556 | GA | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0073 a0001c0001t0001g0107 others(8): Show |
13 | HG01934.hp2 HG02723.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.244+737delT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40847556 | |||||||
| chr22:40847995 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.244+299G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40847995 | |||||||
| chr22:40848184 | A | T | 1 | a0001c0001t0005g0061 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.244+110T>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40848184 | |||||||
| chr22:40848253 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0194 |
4 | HG02280.hp1 HG03130.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+41T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 3/11 | chr22 | 40848253 | |||||||
| chr22:40848394 | C | G | 52 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(49): Show |
94 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.169-25G>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40848394 | |||||||
| chr22:40848451 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.169-82T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40848451 | |||||||
| chr22:40848553 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.169-184G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40848553 | |||||||
| chr22:40848757 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.169-388T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40848757 | |||||||
| chr22:40848760 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.169-391A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40848760 | |||||||
| chr22:40849019 | A | C | 1 | a0003c0003t0001g0031 | 2 | HG00140.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.169-650T>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849019 | |||||||
| chr22:40849038 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.169-669T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849038 | |||||||
| chr22:40849125 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.169-756A>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849125 | |||||||
| chr22:40849149 | T | C | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(6): Show |
15 | HG02155.hp1 NA18942.hp2 NA18944.hp2 others(12): Show |
intron_variant | MODIFIER | c.169-780A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849149 | |||||||
| chr22:40849222 | A | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(15): Show |
24 | HG00639.hp2 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.169-853T>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849222 | |||||||
| chr22:40849453 | C | G | 24 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0081 others(21): Show |
42 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.169-1084G>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849453 | |||||||
| chr22:40849479 | C | CA | 25 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0040 others(22): Show |
32 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.169-1111dupT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849479 | |||||||
| chr22:40849479 | CA | C | 20 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(17): Show |
24 | HG00323.hp2 HG01070.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.169-1111delT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849479 | |||||||
| chr22:40849479 | CAA | C | 31 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(28): Show |
54 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.169-1112_169-1111d others(4): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849479 | |||||||
| chr22:40849479 | CAAA | C | 5 | a0001c0001t0001g0093 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
6 | HG00639.hp2 HG02109.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-1113_169-1111d others(5): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849479 | |||||||
| chr22:40849479 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0150 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.169-1120_169-1111d others(12): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849479 | |||||||
| chr22:40849479 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0104 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.169-1122_169-1111d others(14): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849479 | |||||||
| chr22:40849586 | T | C | 12 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(9): Show |
17 | HG01167.hp2 HG03710.hp2 NA18940.hp2 others(14): Show |
intron_variant | MODIFIER | c.169-1217A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849586 | |||||||
| chr22:40849591 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.169-1222T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849591 | |||||||
| chr22:40849778 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.168+1045G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849778 | |||||||
| chr22:40849912 | C | CA | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.168+910dupT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849912 | |||||||
| chr22:40849912 | C | CAA | 18 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0068 others(15): Show |
23 | HG00639.hp2 HG01346.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.168+909_168+910dup others(2): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40849912 | |||||||
| chr22:40850019 | C | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(46): Show |
75 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.168+804G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40850019 | |||||||
| chr22:40850207 | G | A | 24 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0081 others(21): Show |
42 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.168+616C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40850207 | |||||||
| chr22:40850244 | T | C | 2 | a0001c0001t0006g0020 a0001c0001t0012g0060 |
3 | HG02886.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.168+579A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40850244 | |||||||
| chr22:40850436 | A | G | 5 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(2): Show |
6 | HG01934.hp2 HG02809.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+387T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40850436 | |||||||
| chr22:40850556 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.168+267C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40850556 | |||||||
| chr22:40850650 | C | T | 1 | a0002c0002t0001g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.168+173G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40850650 | |||||||
| chr22:40850660 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0009g0030 |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+163G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40850660 | |||||||
| chr22:40850685 | A | G | 5 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(2): Show |
6 | HG01934.hp2 HG02809.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+138T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40850685 | |||||||
| chr22:40850778 | T | G | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0009g0030 |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+45A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 2/11 | chr22 | 40850778 | |||||||
| chr22:40850948 | C | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(46): Show |
75 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.111-68G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40850948 | |||||||
| chr22:40851157 | GAA | G | 22 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(19): Show |
29 | HG01884.hp1 HG01891.hp1 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.111-279_111-278del others(2): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40851157 | |||||||
| chr22:40851239 | C | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(46): Show |
75 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.111-359G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40851239 | |||||||
| chr22:40851340 | T | G | 1 | a0001c0001t0007g0042 | 2 | HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.111-460A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40851340 | |||||||
| chr22:40851371 | T | G | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-491A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40851371 | |||||||
| chr22:40851455 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0009g0030 |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-575G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40851455 | |||||||
| chr22:40851517 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.111-637C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40851517 | |||||||
| chr22:40851659 | A | G | 1 | a0001c0001t0001g0054 | 2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.111-779T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40851659 | |||||||
| chr22:40851744 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.111-864C>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40851744 | |||||||
| chr22:40851748 | C | CT | 7 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0003c0003t0001g0031 others(4): Show |
11 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.111-869dupA | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40851748 | |||||||
| chr22:40851748 | C | CTT | 4 | a0001c0001t0003g0009 a0001c0001t0003g0056 a0001c0001t0003g0198 others(1): Show |
8 | NA18949.hp2 NA18969.hp2 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.111-870_111-869dup others(2): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40851748 | |||||||
| chr22:40851891 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.111-1011A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40851891 | |||||||
| chr22:40851934 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.111-1054T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40851934 | |||||||
| chr22:40852027 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.111-1147T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40852027 | |||||||
| chr22:40852076 | C | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(46): Show |
75 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.111-1196G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40852076 | |||||||
| chr22:40852078 | T | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(12): Show |
20 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.111-1198A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40852078 | |||||||
| chr22:40852377 | T | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(12): Show |
20 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.111-1497A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40852377 | |||||||
| chr22:40852380 | T | C | 6 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG00099.hp1 HG01433.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-1500A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40852380 | |||||||
| chr22:40852400 | T | C | 1 | a0001c0001t0001g0053 | 2 | NA18979.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.111-1520A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40852400 | |||||||
| chr22:40852501 | A | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(46): Show |
75 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.111-1621T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40852501 | |||||||
| chr22:40852534 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.111-1654C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40852534 | |||||||
| chr22:40852561 | A | C | 1 | a0003c0003t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.111-1681T>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40852561 | |||||||
| chr22:40852575 | A | G | 7 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(4): Show |
9 | HG01934.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-1695T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40852575 | |||||||
| chr22:40852960 | G | A | 1 | a0001c0001t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.111-2080C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40852960 | |||||||
| chr22:40852961 | A | G | 1 | a0001c0001t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.111-2081T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40852961 | |||||||
| chr22:40853244 | A | G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(12): Show |
20 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.111-2364T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40853244 | |||||||
| chr22:40853342 | C | CA | 8 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0144 others(5): Show |
11 | HG02055.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.111-2463dupT | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40853342 | |||||||
| chr22:40853457 | A | T | 1 | a0001c0001t0001g0145 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.111-2577T>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40853457 | |||||||
| chr22:40853518 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.111-2638T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40853518 | |||||||
| chr22:40853544 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG00642.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.111-2664A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40853544 | |||||||
| chr22:40853600 | A | C | 1 | a0003c0003t0001g0031 | 2 | HG00140.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.111-2720T>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40853600 | |||||||
| chr22:40853833 | A | G | 2 | a0001c0001t0006g0020 a0001c0001t0012g0060 |
3 | HG02886.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.110+2598T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40853833 | |||||||
| chr22:40853842 | C | G | 13 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0025 others(10): Show |
30 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.110+2589G>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40853842 | |||||||
| chr22:40853846 | C | A | 1 | a0001c0001t0001g0097 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.110+2585G>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40853846 | |||||||
| chr22:40853861 | T | A | 5 | a0001c0001t0004g0028 a0001c0001t0004g0085 a0001c0001t0004g0086 others(2): Show |
6 | HG01243.hp1 HG01496.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+2570A>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40853861 | |||||||
| chr22:40853867 | G | A | 7 | a0001c0001t0005g0029 a0001c0001t0005g0061 a0001c0001t0005g0062 others(4): Show |
9 | HG01934.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.110+2564C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40853867 | |||||||
| chr22:40853923 | T | C | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0009g0030 |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+2508A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40853923 | |||||||
| chr22:40854130 | C | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0069 others(46): Show |
75 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.110+2301G>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40854130 | |||||||
| chr22:40854206 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.110+2225T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40854206 | |||||||
| chr22:40854358 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.110+2073T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40854358 | |||||||
| chr22:40854435 | G | T | 24 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0081 others(21): Show |
42 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.110+1996C>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40854435 | |||||||
| chr22:40854465 | G | A | 1 | a0002c0002t0001g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.110+1966C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40854465 | |||||||
| chr22:40854533 | C | A | 1 | a0001c0001t0002g0185 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.110+1898G>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40854533 | |||||||
| chr22:40854570 | A | T | 1 | a0002c0002t0001g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.110+1861T>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40854570 | |||||||
| chr22:40854707 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0069 a0001c0001t0001g0071 others(2): Show |
7 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+1724G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40854707 | |||||||
| chr22:40855008 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0066 others(2): Show |
7 | HG01106.hp2 HG01346.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+1423G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855008 | |||||||
| chr22:40855175 | G | T | 2 | a0001c0001t0006g0020 a0001c0001t0012g0060 |
3 | HG02886.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.110+1256C>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855175 | |||||||
| chr22:40855328 | A | T | 1 | a0001c0001t0002g0065 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.110+1103T>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855328 | |||||||
| chr22:40855500 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.110+931A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855500 | |||||||
| chr22:40855873 | A | T | 12 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0190 others(9): Show |
17 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.110+558T>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855873 | |||||||
| chr22:40855874 | A | G | 12 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0190 others(9): Show |
17 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.110+557T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855874 | |||||||
| chr22:40855875 | G | GACAGTGT | 12 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0190 others(9): Show |
17 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.110+555_110+556ins others(7): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855875 | |||||||
| chr22:40855878 | A | T | 12 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0190 others(9): Show |
17 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.110+553T>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855878 | |||||||
| chr22:40855880 | G | C | 12 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0190 others(9): Show |
17 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.110+551C>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855880 | |||||||
| chr22:40855884 | G | T | 12 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0190 others(9): Show |
17 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.110+547C>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855884 | |||||||
| chr22:40855885 | T | TACTTG | 12 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0190 others(9): Show |
17 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.110+545_110+546ins others(5): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855885 | |||||||
| chr22:40855887 | T | G | 12 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0190 others(9): Show |
17 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.110+544A>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855887 | |||||||
| chr22:40855914 | C | G | 1 | a0001c0001t0001g0021 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.110+517G>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855914 | |||||||
| chr22:40855920 | C | T | 6 | a0001c0001t0005g0061 a0001c0001t0005g0062 a0001c0001t0006g0020 others(3): Show |
7 | HG02809.hp1 HG02886.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.110+511G>A | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855920 | |||||||
| chr22:40855938 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.110+493C>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40855938 | |||||||
| chr22:40856010 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0058 |
4 | HG02965.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+421T>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40856010 | |||||||
| chr22:40856120 | TAA | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0059 |
3 | NA18950.hp2 NA19056.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.110+309_110+310del others(2): Show |
ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40856120 | |||||||
| chr22:40856287 | T | C | 1 | a0001c0001t0001g0055 | 2 | HG00099.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.110+144A>G | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40856287 | |||||||
| chr22:40856299 | G | A | 1 | a0001c0001t0015g0197 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.110+132C>T | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40856299 | |||||||
| chr22:40856401 | C | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0058 |
4 | HG02965.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+30G>C | ST13 | ENSG00000100380.15 | transcript | ENST00000216218.8 | protein_coding | 1/11 | chr22 | 40856401 |