Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11198 |
| ensemblid | ENSG00000092201.10 |
| hgncid | 11465 |
| symbol | SUPT16H |
| name | SPT16 homolog, facilitates chromatin remodeling subunit |
| refseq_nuc | NM_007192.4 |
| refseq_prot | NP_009123.1 |
| ensembl_nuc | ENST00000216297.7 |
| ensembl_prot | ENSP00000216297.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 21351476 |
| end | 21384019 |
| strand | - |
| ver | v1.2 |
| region | chr14:21351476-21384019 |
| region5000 | chr14:21346476-21389019 |
| regionname0 | SUPT16H_chr14_21351476_21384019 |
| regionname5000 | SUPT16H_chr14_21346476_21389019 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1047 | 306 | 94 | 54 | 124 | 14 | 18 | 94 | SUPT16H_chr14_21346476_21389019 | SUPT16H | MAVTL others(1042): Show |
chr14 | 21346476 | 21389019 |
| a0002 | 0/0 | 1047 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | MAVTL others(1042): Show |
chr14 | 21346476 | 21389019 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3141 | 205 | 42 | 35 | 105 | 12 | 10 | SUPT16H_chr14_21346476_21389019 | SUPT16H | ATGGC others(3136): Show |
chr14 | 21346476 | 21389019 | ||
| a0001c0002 | 1/0 | 3141 | 57 | 17 | 14 | 16 | 2 | 7 | SUPT16H_chr14_21346476_21389019 | SUPT16H | ATGGC others(3136): Show |
chr14 | 21346476 | 21389019 | ||
| a0001c0003 | 0/0 | 3141 | 11 | 11 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | ATGGC others(3136): Show |
chr14 | 21346476 | 21389019 | ||
| a0001c0004 | 0/0 | 3141 | 11 | 10 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | ATGGC others(3136): Show |
chr14 | 21346476 | 21389019 | ||
| a0001c0005 | 0/0 | 3141 | 9 | 8 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | ATGGC others(3136): Show |
chr14 | 21346476 | 21389019 | ||
| a0001c0006 | 0/0 | 3141 | 4 | 0 | 3 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | ATGGC others(3136): Show |
chr14 | 21346476 | 21389019 | ||
| a0001c0007 | 0/0 | 3141 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | ATGGC others(3136): Show |
chr14 | 21346476 | 21389019 | ||
| a0001c0008 | 0/0 | 3141 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | ATGGC others(3136): Show |
chr14 | 21346476 | 21389019 | ||
| a0001c0009 | 0/0 | 3141 | 2 | 0 | 0 | 2 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | ATGGC others(3136): Show |
chr14 | 21346476 | 21389019 | ||
| a0001c0011 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | ATGGC others(3136): Show |
chr14 | 21346476 | 21389019 | ||
| a0001c0012 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | ATGGC others(3136): Show |
chr14 | 21346476 | 21389019 | ||
| a0001c0013 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | ATGGC others(3136): Show |
chr14 | 21346476 | 21389019 | ||
| a0002c0010 | 0/0 | 3141 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | ATGGC others(3136): Show |
chr14 | 21346476 | 21389019 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4433 | 169 | 38 | 28 | 82 | 10 | 10 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0001t0002 | 0/0 | 4433 | 3 | 0 | 0 | 3 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0001t0003 | 0/0 | 4433 | 21 | 4 | 0 | 17 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0001t0004 | 0/0 | 4433 | 9 | 0 | 7 | 0 | 2 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0001t0006 | 0/0 | 4433 | 3 | 0 | 0 | 3 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0002t0001 | 0/0 | 4433 | 16 | 16 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0002t0002 | 1/0 | 4433 | 39 | 0 | 14 | 15 | 2 | 7 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0002t0009 | 0/0 | 4433 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0002t0010 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0003t0001 | 0/0 | 4433 | 7 | 7 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0003t0005 | 0/0 | 4433 | 3 | 3 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0003t0013 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0004t0001 | 0/0 | 4433 | 10 | 10 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0004t0012 | 0/0 | 4433 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0005t0001 | 0/0 | 4433 | 8 | 7 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0005t0011 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0006t0001 | 0/0 | 4433 | 4 | 0 | 3 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0007t0008 | 0/0 | 4433 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0008t0001 | 0/0 | 4433 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0009t0001 | 0/0 | 4433 | 2 | 0 | 0 | 2 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0011t0001 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0012t0002 | 0/0 | 4433 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0001c0013t0001 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| a0002c0010t0007 | 0/0 | 4433 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | GGGAG others(4428): Show |
chr14 | 21346476 | 21389019 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 15 | 0 | 3 | 11 | 1 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0006 | 0/0 | 6 | 2 | 0 | 2 | 2 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0004g0005 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0006g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0001 | 1/0 | 16 | 0 | 3 | 10 | 0 | 2 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0004 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0009g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0002t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0003t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0003t0005g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0003t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0003t0013g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0004t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0004t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0004t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0004t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0004t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0004t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0004t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0004t0012g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0005t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0005t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0005t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0005t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0005t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0005t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0005t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0005t0011g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0006t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0006t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0007t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0007t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0008t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0008t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0009t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0009t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0011t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0012t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0001c0013t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| a0002c0010t0007g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0005 | EUR | GBR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | GBR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0091 | EUR | GBR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | GBR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0060 | EUR | FIN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0061 | EUR | FIN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | CHS | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00733 | hp2 | a0001 | c0006 | t0001 | g0028 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00735 | hp1 | a0001 | c0006 | t0001 | g0027 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01243 | hp2 | a0001 | c0005 | t0001 | g0054 | AMR | PUR | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01261 | hp2 | a0001 | c0004 | t0012 | g0082 | AMR | CLM | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01361 | hp1 | a0001 | c0006 | t0001 | g0028 | AMR | CLM | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0017 | AMR | CLM | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01884 | hp2 | a0001 | c0004 | t0001 | g0078 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01891 | hp1 | a0001 | c0013 | t0001 | g0166 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0094 | AMR | PEL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0071 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02145 | hp1 | a0001 | c0007 | t0008 | g0076 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0092 | AMR | PEL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02257 | hp1 | a0001 | c0004 | t0001 | g0080 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0064 | AMR | PEL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02451 | hp1 | a0001 | c0004 | t0001 | g0079 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0142 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02615 | hp2 | a0001 | c0007 | t0008 | g0077 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02622 | hp1 | a0001 | c0008 | t0001 | g0046 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0099 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0018 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0017 | SAS | PJL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0206 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0081 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02896 | hp1 | a0001 | c0003 | t0005 | g0190 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02897 | hp2 | a0001 | c0003 | t0005 | g0037 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0029 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02965 | hp1 | a0001 | c0005 | t0011 | g0070 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02965 | hp2 | a0001 | c0003 | t0005 | g0037 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02970 | hp1 | a0001 | c0004 | t0001 | g0018 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03041 | hp2 | a0001 | c0004 | t0001 | g0040 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03098 | hp1 | a0001 | c0005 | t0001 | g0075 | AFR | MSL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | MSL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03130 | hp1 | a0001 | c0002 | t0010 | g0065 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03139 | hp1 | a0002 | c0010 | t0007 | g0041 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0203 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03209 | hp2 | a0001 | c0005 | t0001 | g0053 | AFR | MSL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03225 | hp1 | a0002 | c0010 | t0007 | g0041 | AFR | MSL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03225 | hp2 | a0001 | c0011 | t0001 | g0068 | AFR | MSL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | MSL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | MSL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03516 | hp2 | a0001 | c0005 | t0001 | g0072 | AFR | ESN | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0204 | AFR | MSL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0100 | AFR | MSL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0058 | SAS | PJL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0042 | SAS | PJL | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG03927 | hp2 | a0001 | c0006 | t0001 | g0027 | SAS | BEB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0069 | SAS | BEB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0044 | SAS | STU | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | CHB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0074 | AFR | YRI | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18950 | hp1 | a0001 | c0009 | t0001 | g0106 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19004 | hp2 | a0001 | c0012 | t0002 | g0056 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19005 | hp2 | a0001 | c0002 | t0009 | g0062 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0188 | AFR | LWK | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0073 | AFR | LWK | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19056 | hp1 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19076 | hp1 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19076 | hp2 | a0001 | c0009 | t0001 | g0148 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0172 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | YRI | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA19240 | hp2 | a0001 | c0003 | t0013 | g0189 | AFR | YRI | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | ASW | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ASW | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | TSI | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | TSI | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0067 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0040 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG02559 | hp2 | a0001 | c0008 | t0001 | g0047 | AFR | ACB | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | USA | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | USA | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | USA | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0170 | REF | REF | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0001 | REF | REF | SUPT16H_chr14_21346476_21389019 | SUPT16H | chr14 | 21346476 | 21389019 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:21363493 | G | C | 1 | a0002 | 2 | HG03139.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.1244C>G | p.Ala415Gly | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 11/26 | 1336/4433 | 1244/3144 | 415/1047 | chr14 | 21363493 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:21353513 | A | G | 1 | a0001c0008 | 2 | HG02559.hp2 HG02622.hp1 |
synonymous_variant | LOW | c.2973T>C | p.Asp991Asp | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 25/26 | 3065/4433 | 2973/3144 | 991/1047 | chr14 | 21353513 | |||
| chr14:21357241 | G | A | 1 | a0001c0011 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.2616C>T | p.Asn872Asn | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/26 | 2708/4433 | 2616/3144 | 872/1047 | chr14 | 21357241 | |||
| chr14:21357271 | C | T | 1 | a0001c0009 | 2 | NA18950.hp1 NA19076.hp2 |
synonymous_variant | LOW | c.2586G>A | p.Lys862Lys | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/26 | 2678/4433 | 2586/3144 | 862/1047 | chr14 | 21357271 | |||
| chr14:21357328 | G | T | 1 | a0001c0013 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.2529C>A | p.Ile843Ile | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/26 | 2621/4433 | 2529/3144 | 843/1047 | chr14 | 21357328 | |||
| chr14:21359604 | G | A | 1 | a0001c0007 | 2 | HG02145.hp1 HG02615.hp2 |
synonymous_variant | LOW | c.2181C>T | p.Ala727Ala | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 19/26 | 2273/4433 | 2181/3144 | 727/1047 | chr14 | 21359604 | |||
| chr14:21360970 | C | G | 8 | a0001c0001 a0001c0003 a0001c0004 others(5): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
splice_region_variant&synonymous_variant | LOW | c.1932G>C | p.Gly644Gly | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 17/26 | 2024/4433 | 1932/3144 | 644/1047 | chr14 | 21360970 | |||
| chr14:21362285 | G | T | 1 | a0001c0012 | 1 | NA19004.hp2 | synonymous_variant | LOW | c.1705C>A | p.Arg569Arg | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/26 | 1797/4433 | 1705/3144 | 569/1047 | chr14 | 21362285 | |||
| chr14:21362893 | T | C | 5 | a0001c0001 a0001c0003 a0001c0006 others(2): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
synonymous_variant | LOW | c.1566A>G | p.Pro522Pro | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 14/26 | 1658/4433 | 1566/3144 | 522/1047 | chr14 | 21362893 | |||
| chr14:21363260 | C | T | 1 | a0001c0006 | 4 | HG00733.hp2 HG00735.hp1 HG01361.hp1 others(1): Show |
synonymous_variant | LOW | c.1368G>A | p.Arg456Arg | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 12/26 | 1460/4433 | 1368/3144 | 456/1047 | chr14 | 21363260 | |||
| chr14:21371928 | C | T | 1 | a0001c0003 | 11 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(8): Show |
synonymous_variant | LOW | c.276G>A | p.Lys92Lys | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/26 | 368/4433 | 276/3144 | 92/1047 | chr14 | 21371928 | |||
| chr14:21373365 | A | G | 2 | a0001c0005 a0001c0011 |
10 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
synonymous_variant | LOW | c.132T>C | p.Ile44Ile | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 2/26 | 224/4433 | 132/3144 | 44/1047 | chr14 | 21373365 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:21351525 | C | A | 1 | a0001c0003t0005 | 3 | HG02896.hp1 HG02897.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1148G>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 26/26 | 1148 | chr14 | 21351525 | ||||||
| chr14:21351684 | G | C | 1 | a0001c0005t0011 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*989C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 26/26 | 989 | chr14 | 21351684 | ||||||
| chr14:21351857 | G | T | 1 | a0001c0002t0010 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*816C>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 26/26 | 816 | chr14 | 21351857 | ||||||
| chr14:21351870 | A | C | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(17): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*803T>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 26/26 | 803 | chr14 | 21351870 | ||||||
| chr14:21351920 | C | T | 1 | a0002c0010t0007 | 2 | HG03139.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*753G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 26/26 | 753 | chr14 | 21351920 | ||||||
| chr14:21351960 | A | G | 1 | a0001c0007t0008 | 2 | HG02145.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*713T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 26/26 | 713 | chr14 | 21351960 | ||||||
| chr14:21352014 | T | C | 1 | a0001c0004t0012 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*659A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 26/26 | 659 | chr14 | 21352014 | ||||||
| chr14:21352034 | G | A | 1 | a0001c0003t0005 | 3 | HG02896.hp1 HG02897.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*639C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 26/26 | 639 | chr14 | 21352034 | ||||||
| chr14:21352295 | G | C | 2 | a0001c0001t0003 a0001c0001t0006 |
24 | HG00438.hp1 HG02280.hp1 HG02486.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*378C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 26/26 | 378 | chr14 | 21352295 | ||||||
| chr14:21352417 | T | C | 1 | a0001c0003t0013 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*256A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 26/26 | 256 | chr14 | 21352417 | ||||||
| chr14:21352492 | G | A | 1 | a0001c0007t0008 | 2 | HG02145.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*181C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 26/26 | 181 | chr14 | 21352492 | ||||||
| chr14:21352510 | A | C | 1 | a0001c0001t0004 | 9 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*163T>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 26/26 | 163 | chr14 | 21352510 | ||||||
| chr14:21352597 | A | G | 1 | a0001c0002t0009 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*76T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 26/26 | 76 | chr14 | 21352597 | ||||||
| chr14:21352614 | T | C | 1 | a0001c0001t0006 | 3 | NA19056.hp1 NA19076.hp1 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*59A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 26/26 | 59 | chr14 | 21352614 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:21352829 | G | C | 1 | a0001c0005t0011g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2999-11C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 25/25 | chr14 | 21352829 | |||||||
| chr14:21352990 | G | T | 6 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 others(3): Show |
8 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2999-172C>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 25/25 | chr14 | 21352990 | |||||||
| chr14:21353054 | A | G | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2999-236T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 25/25 | chr14 | 21353054 | |||||||
| chr14:21353084 | G | C | 1 | a0001c0002t0002g0063 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2999-266C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 25/25 | chr14 | 21353084 | |||||||
| chr14:21353662 | A | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0025 others(42): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2920+41T>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 24/25 | chr14 | 21353662 | |||||||
| chr14:21354628 | G | A | 6 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 others(3): Show |
8 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2661-88C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21354628 | |||||||
| chr14:21354633 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2661-93G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21354633 | |||||||
| chr14:21354643 | G | A | 1 | a0001c0004t0001g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2661-103C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21354643 | |||||||
| chr14:21354762 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2661-222A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21354762 | |||||||
| chr14:21354955 | C | G | 1 | a0001c0004t0012g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2661-415G>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21354955 | |||||||
| chr14:21354958 | G | C | 6 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 others(3): Show |
8 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2661-418C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21354958 | |||||||
| chr14:21355108 | CCT | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0083 |
3 | HG02976.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2661-570_2661-569d others(4): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355108 | |||||||
| chr14:21355116 | T | A | 5 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0079 others(2): Show |
6 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2661-576A>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355116 | |||||||
| chr14:21355121 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2661-581C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355121 | |||||||
| chr14:21355270 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0001g0186 others(1): Show |
6 | HG02630.hp1 HG02818.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2661-730C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355270 | |||||||
| chr14:21355354 | A | G | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2661-814T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355354 | |||||||
| chr14:21355379 | G | A | 1 | a0001c0005t0001g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2661-839C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355379 | |||||||
| chr14:21355379 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0095 |
3 | HG02145.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2661-839C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355379 | |||||||
| chr14:21355448 | G | A | 1 | a0001c0002t0001g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2661-908C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355448 | |||||||
| chr14:21355513 | TA | T | 19 | a0001c0002t0001g0206 a0001c0002t0002g0059 a0001c0002t0002g0061 others(16): Show |
21 | HG00323.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2661-974delT | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355513 | |||||||
| chr14:21355513 | TAA | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0101 others(5): Show |
12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2661-975_2661-974d others(4): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355513 | |||||||
| chr14:21355513 | TAAA | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0019 others(46): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.2661-976_2661-974d others(5): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355513 | |||||||
| chr14:21355513 | TAAAA | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(70): Show |
113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2661-977_2661-974d others(6): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355513 | |||||||
| chr14:21355513 | TAAAAA | T | 24 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0115 others(21): Show |
28 | HG00438.hp1 HG01070.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.2661-978_2661-974d others(7): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355513 | |||||||
| chr14:21355517 | A | T | 7 | a0001c0004t0001g0040 a0001c0004t0001g0078 a0001c0004t0001g0080 others(4): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2661-977T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355517 | |||||||
| chr14:21355518 | A | T | 3 | a0001c0004t0001g0018 a0001c0007t0008g0076 a0001c0007t0008g0077 |
4 | HG02145.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2661-978T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355518 | |||||||
| chr14:21355520 | A | T | 1 | a0002c0010t0007g0041 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2661-980T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355520 | |||||||
| chr14:21355533 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0101 others(2): Show |
8 | HG01884.hp1 HG01891.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2661-993T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355533 | |||||||
| chr14:21355564 | C | G | 1 | a0001c0004t0012g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2661-1024G>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355564 | |||||||
| chr14:21355857 | A | C | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2661-1317T>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21355857 | |||||||
| chr14:21356124 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.2660+1073C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21356124 | |||||||
| chr14:21356163 | G | C | 10 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0043 others(7): Show |
15 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2660+1034C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21356163 | |||||||
| chr14:21356236 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2660+961A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21356236 | |||||||
| chr14:21356291 | T | C | 1 | a0001c0004t0001g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2660+906A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21356291 | |||||||
| chr14:21356370 | C | T | 1 | a0002c0010t0007g0041 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2660+827G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21356370 | |||||||
| chr14:21356414 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2660+783T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21356414 | |||||||
| chr14:21356442 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2660+755C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21356442 | |||||||
| chr14:21356554 | T | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0201 |
2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2660+643A>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21356554 | |||||||
| chr14:21356744 | A | AACC | 2 | a0001c0006t0001g0027 a0001c0006t0001g0028 |
4 | HG00733.hp2 HG00735.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.2660+450_2660+452d others(5): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21356744 | |||||||
| chr14:21356897 | G | A | 1 | a0001c0002t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2660+300C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21356897 | |||||||
| chr14:21356966 | G | T | 1 | a0001c0001t0001g0011 | 3 | HG02257.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2660+231C>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 22/25 | chr14 | 21356966 | |||||||
| chr14:21357414 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0001g0186 others(1): Show |
6 | HG02630.hp1 HG02818.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2491-48C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 21/25 | chr14 | 21357414 | |||||||
| chr14:21357483 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2491-117A>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 21/25 | chr14 | 21357483 | |||||||
| chr14:21357526 | C | G | 3 | a0001c0001t0003g0173 a0001c0001t0003g0174 a0001c0001t0003g0175 |
3 | NA18946.hp1 NA18964.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.2491-160G>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 21/25 | chr14 | 21357526 | |||||||
| chr14:21357684 | C | T | 1 | a0001c0004t0012g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2490+243G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 21/25 | chr14 | 21357684 | |||||||
| chr14:21357765 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.2490+162A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 21/25 | chr14 | 21357765 | |||||||
| chr14:21357816 | A | G | 1 | a0002c0010t0007g0041 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2490+111T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 21/25 | chr14 | 21357816 | |||||||
| chr14:21358153 | C | T | 1 | a0001c0002t0002g0060 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2415-151G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 20/25 | chr14 | 21358153 | |||||||
| chr14:21358559 | T | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(184): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.2302-132A>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 19/25 | chr14 | 21358559 | |||||||
| chr14:21358584 | G | A | 4 | a0001c0002t0001g0066 a0001c0002t0010g0065 a0001c0008t0001g0046 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2302-157C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 19/25 | chr14 | 21358584 | |||||||
| chr14:21358741 | C | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(155): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2302-314G>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 19/25 | chr14 | 21358741 | |||||||
| chr14:21358744 | G | C | 1 | a0001c0002t0001g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2302-317C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 19/25 | chr14 | 21358744 | |||||||
| chr14:21358800 | G | GTTTA | 5 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0079 others(2): Show |
6 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2302-377_2302-374d others(6): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 19/25 | chr14 | 21358800 | |||||||
| chr14:21359030 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2301+454G>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 19/25 | chr14 | 21359030 | |||||||
| chr14:21359120 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2301+364A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 19/25 | chr14 | 21359120 | |||||||
| chr14:21359137 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2301+347C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 19/25 | chr14 | 21359137 | |||||||
| chr14:21359184 | G | C | 10 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0043 others(7): Show |
15 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2301+300C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 19/25 | chr14 | 21359184 | |||||||
| chr14:21359252 | G | A | 1 | a0001c0002t0002g0045 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2301+232C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 19/25 | chr14 | 21359252 | |||||||
| chr14:21359387 | C | T | 1 | a0002c0010t0007g0041 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2301+97G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 19/25 | chr14 | 21359387 | |||||||
| chr14:21359418 | C | T | 1 | a0001c0002t0002g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2301+66G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 19/25 | chr14 | 21359418 | |||||||
| chr14:21359769 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2176-160C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 18/25 | chr14 | 21359769 | |||||||
| chr14:21360060 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2175+355G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 18/25 | chr14 | 21360060 | |||||||
| chr14:21360145 | G | T | 1 | a0001c0004t0001g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2175+270C>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 18/25 | chr14 | 21360145 | |||||||
| chr14:21360274 | C | G | 1 | a0001c0002t0002g0016 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2175+141G>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 18/25 | chr14 | 21360274 | |||||||
| chr14:21360361 | T | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(180): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2175+54A>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 18/25 | chr14 | 21360361 | |||||||
| chr14:21360686 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2057-153T>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 17/25 | chr14 | 21360686 | |||||||
| chr14:21361245 | T | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(151): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1794-32A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361245 | |||||||
| chr14:21361259 | G | A | 1 | a0002c0010t0007g0041 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1794-46C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361259 | |||||||
| chr14:21361259 | G | C | 1 | a0001c0002t0001g0051 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1794-46C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361259 | |||||||
| chr14:21361311 | C | CT | 58 | a0001c0001t0001g0019 a0001c0001t0001g0083 a0001c0001t0001g0086 others(55): Show |
70 | HG00609.hp2 HG00733.hp2 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.1794-99dupA | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361311 | |||||||
| chr14:21361311 | C | CTT | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(81): Show |
129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1794-100_1794-99du others(3): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361311 | |||||||
| chr14:21361311 | C | CTTT | 8 | a0001c0001t0001g0030 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
9 | HG00673.hp2 HG01175.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1794-101_1794-99du others(4): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361311 | |||||||
| chr14:21361311 | CTT | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0124 others(6): Show |
15 | HG00544.hp1 HG00673.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.1794-100_1794-99de others(3): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361311 | |||||||
| chr14:21361311 | CTTTTT | C | 6 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 others(3): Show |
8 | HG01261.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1794-103_1794-99de others(6): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361311 | |||||||
| chr14:21361385 | T | C | 1 | a0002c0010t0007g0041 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1794-172A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361385 | |||||||
| chr14:21361390 | C | T | 1 | a0001c0008t0001g0046 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1794-177G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361390 | |||||||
| chr14:21361527 | G | A | 4 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0080 others(1): Show |
5 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1794-314C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361527 | |||||||
| chr14:21361560 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1794-347C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361560 | |||||||
| chr14:21361597 | G | A | 2 | a0001c0007t0008g0076 a0001c0007t0008g0077 |
2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1794-384C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361597 | |||||||
| chr14:21361730 | C | T | 1 | a0001c0002t0001g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1793+467G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361730 | |||||||
| chr14:21361776 | T | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0019 others(48): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.1793+421A>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361776 | |||||||
| chr14:21361863 | G | T | 1 | a0001c0013t0001g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1793+334C>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361863 | |||||||
| chr14:21361923 | C | A | 5 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0079 others(2): Show |
6 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1793+274G>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21361923 | |||||||
| chr14:21362181 | T | C | 4 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0080 others(1): Show |
5 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1793+16A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 15/25 | chr14 | 21362181 | |||||||
| chr14:21362400 | A | C | 1 | a0002c0010t0007g0041 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1666-76T>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 14/25 | chr14 | 21362400 | |||||||
| chr14:21362476 | C | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1666-152G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 14/25 | chr14 | 21362476 | |||||||
| chr14:21362528 | A | G | 1 | a0001c0005t0001g0054 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1666-204T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 14/25 | chr14 | 21362528 | |||||||
| chr14:21362752 | A | T | 1 | a0001c0004t0012g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1665+42T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 14/25 | chr14 | 21362752 | |||||||
| chr14:21362757 | C | T | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1665+37G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 14/25 | chr14 | 21362757 | |||||||
| chr14:21362953 | G | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
splice_region_variant&intron_variant | LOW | c.1512-6C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 13/25 | chr14 | 21362953 | |||||||
| chr14:21363361 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1300-33A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 11/25 | chr14 | 21363361 | |||||||
| chr14:21363387 | A | T | 2 | a0001c0002t0001g0066 a0001c0002t0010g0065 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1299+51T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 11/25 | chr14 | 21363387 | |||||||
| chr14:21363507 | G | A | 3 | a0001c0002t0002g0004 a0001c0002t0002g0016 a0001c0002t0002g0064 |
10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1234-4C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 10/25 | chr14 | 21363507 | |||||||
| chr14:21363533 | T | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(159): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1234-30A>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 10/25 | chr14 | 21363533 | |||||||
| chr14:21363585 | T | C | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-82A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 10/25 | chr14 | 21363585 | |||||||
| chr14:21363646 | C | T | 1 | a0001c0004t0012g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1234-143G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 10/25 | chr14 | 21363646 | |||||||
| chr14:21363771 | C | T | 1 | a0001c0004t0012g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1234-268G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 10/25 | chr14 | 21363771 | |||||||
| chr14:21363826 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1234-323C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 10/25 | chr14 | 21363826 | |||||||
| chr14:21364175 | T | C | 1 | a0001c0003t0001g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1233+652A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 10/25 | chr14 | 21364175 | |||||||
| chr14:21364231 | C | CCT | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(184): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1233+595_1233+596i others(4): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 10/25 | chr14 | 21364231 | |||||||
| chr14:21364288 | C | G | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+539G>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 10/25 | chr14 | 21364288 | |||||||
| chr14:21364301 | A | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1233+526T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 10/25 | chr14 | 21364301 | |||||||
| chr14:21364614 | G | A | 1 | a0002c0010t0007g0041 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1233+213C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 10/25 | chr14 | 21364614 | |||||||
| chr14:21364617 | C | T | 2 | a0001c0006t0001g0027 a0001c0006t0001g0028 |
4 | HG00733.hp2 HG00735.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+210G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 10/25 | chr14 | 21364617 | |||||||
| chr14:21364783 | G | C | 3 | a0001c0001t0001g0104 a0001c0001t0001g0111 a0001c0001t0001g0117 |
3 | HG01069.hp2 HG01167.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1233+44C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 10/25 | chr14 | 21364783 | |||||||
| chr14:21364988 | G | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1121-49C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 9/25 | chr14 | 21364988 | |||||||
| chr14:21365365 | C | T | 4 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0079 others(1): Show |
5 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-222G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 8/25 | chr14 | 21365365 | |||||||
| chr14:21365436 | G | A | 2 | a0001c0007t0008g0076 a0001c0007t0008g0077 |
2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1047-293C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 8/25 | chr14 | 21365436 | |||||||
| chr14:21365582 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1047-439G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 8/25 | chr14 | 21365582 | |||||||
| chr14:21365759 | C | CAAACCA | 2 | a0001c0004t0001g0040 a0001c0004t0001g0203 |
3 | HG02559.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1047-622_1047-617d others(8): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 8/25 | chr14 | 21365759 | |||||||
| chr14:21365759 | C | CAAACCAA others(5): Show |
1 | a0001c0004t0001g0204 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1047-628_1047-617d others(14): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 8/25 | chr14 | 21365759 | |||||||
| chr14:21365759 | CAAACCA | C | 4 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0080 others(1): Show |
5 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1047-622_1047-617d others(8): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 8/25 | chr14 | 21365759 | |||||||
| chr14:21365788 | C | A | 1 | a0001c0004t0012g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1047-645G>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 8/25 | chr14 | 21365788 | |||||||
| chr14:21365820 | C | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(65): Show |
100 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1046+619G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 8/25 | chr14 | 21365820 | |||||||
| chr14:21366044 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1046+395C>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 8/25 | chr14 | 21366044 | |||||||
| chr14:21366147 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1046+292G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 8/25 | chr14 | 21366147 | |||||||
| chr14:21366353 | A | G | 1 | a0001c0001t0002g0146 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1046+86T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 8/25 | chr14 | 21366353 | |||||||
| chr14:21366598 | C | T | 10 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0043 others(7): Show |
15 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.956-69G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21366598 | |||||||
| chr14:21366656 | C | CTTT | 8 | a0001c0001t0001g0117 a0001c0004t0001g0040 a0001c0004t0001g0203 others(5): Show |
10 | HG01069.hp2 HG01261.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.956-130_956-128dup others(3): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21366656 | |||||||
| chr14:21366656 | C | CTTTT | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(151): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.956-131_956-128dup others(4): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21366656 | |||||||
| chr14:21367010 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(155): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.956-481T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367010 | |||||||
| chr14:21367055 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0114 a0001c0001t0001g0115 |
4 | HG01070.hp1 HG01169.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.956-526C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367055 | |||||||
| chr14:21367061 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.956-532A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367061 | |||||||
| chr14:21367141 | G | A | 5 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0079 others(2): Show |
6 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.956-612C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367141 | |||||||
| chr14:21367167 | A | G | 2 | a0001c0007t0008g0076 a0001c0007t0008g0077 |
2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.956-638T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367167 | |||||||
| chr14:21367198 | C | T | 5 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0079 others(2): Show |
6 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.956-669G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367198 | |||||||
| chr14:21367250 | T | C | 1 | a0001c0004t0012g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.956-721A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367250 | |||||||
| chr14:21367258 | G | A | 1 | a0001c0002t0002g0017 | 2 | HG01496.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.956-729C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367258 | |||||||
| chr14:21367283 | T | C | 1 | a0001c0005t0001g0054 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.956-754A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367283 | |||||||
| chr14:21367480 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.955+789A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367480 | |||||||
| chr14:21367560 | G | C | 1 | a0001c0004t0012g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.955+709C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367560 | |||||||
| chr14:21367602 | C | T | 1 | a0001c0004t0012g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.955+667G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367602 | |||||||
| chr14:21367789 | G | C | 7 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 others(4): Show |
9 | HG01261.hp2 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.955+480C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367789 | |||||||
| chr14:21367893 | T | C | 1 | a0001c0002t0002g0064 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.955+376A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367893 | |||||||
| chr14:21367916 | G | A | 1 | a0001c0002t0001g0052 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.955+353C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367916 | |||||||
| chr14:21367982 | G | A | 1 | a0001c0008t0001g0047 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.955+287C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21367982 | |||||||
| chr14:21368113 | G | C | 1 | a0001c0001t0001g0116 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.955+156C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21368113 | |||||||
| chr14:21368238 | C | T | 3 | a0001c0004t0001g0018 a0001c0004t0001g0080 a0001c0004t0001g0081 |
4 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+31G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21368238 | |||||||
| chr14:21368241 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.955+28A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 7/25 | chr14 | 21368241 | |||||||
| chr14:21368447 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG00741.hp1 | splice_region_variant&intron_variant | LOW | c.783-6C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 6/25 | chr14 | 21368447 | |||||||
| chr14:21368453 | C | T | 7 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 others(4): Show |
9 | HG01261.hp2 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.783-12G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 6/25 | chr14 | 21368453 | |||||||
| chr14:21368504 | T | C | 2 | a0001c0002t0001g0066 a0001c0002t0010g0065 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.783-63A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 6/25 | chr14 | 21368504 | |||||||
| chr14:21368562 | A | G | 1 | a0001c0001t0003g0176 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.783-121T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 6/25 | chr14 | 21368562 | |||||||
| chr14:21368653 | G | C | 1 | a0001c0004t0001g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.783-212C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 6/25 | chr14 | 21368653 | |||||||
| chr14:21368722 | T | C | 1 | a0001c0004t0012g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.783-281A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 6/25 | chr14 | 21368722 | |||||||
| chr14:21368936 | G | A | 2 | a0001c0007t0008g0076 a0001c0007t0008g0077 |
2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.782+268C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 6/25 | chr14 | 21368936 | |||||||
| chr14:21369081 | A | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.782+123T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 6/25 | chr14 | 21369081 | |||||||
| chr14:21369475 | G | A | 1 | a0002c0010t0007g0041 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.631-120C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 5/25 | chr14 | 21369475 | |||||||
| chr14:21369588 | C | T | 1 | a0001c0004t0001g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.630+162G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 5/25 | chr14 | 21369588 | |||||||
| chr14:21369643 | G | A | 1 | a0001c0005t0001g0071 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.630+107C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 5/25 | chr14 | 21369643 | |||||||
| chr14:21369720 | C | G | 2 | a0001c0006t0001g0027 a0001c0006t0001g0028 |
4 | HG00733.hp2 HG00735.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+30G>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 5/25 | chr14 | 21369720 | |||||||
| chr14:21370001 | A | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.484-105T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 4/25 | chr14 | 21370001 | |||||||
| chr14:21370003 | C | G | 1 | a0001c0004t0001g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.484-107G>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 4/25 | chr14 | 21370003 | |||||||
| chr14:21370118 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.483+218G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 4/25 | chr14 | 21370118 | |||||||
| chr14:21370170 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.483+166T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 4/25 | chr14 | 21370170 | |||||||
| chr14:21370204 | C | T | 10 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0043 others(7): Show |
15 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.483+132G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 4/25 | chr14 | 21370204 | |||||||
| chr14:21370509 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.331-21T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21370509 | |||||||
| chr14:21370576 | A | T | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-88T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21370576 | |||||||
| chr14:21370622 | C | T | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(180): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.331-134G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21370622 | |||||||
| chr14:21370655 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.331-167G>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21370655 | |||||||
| chr14:21370656 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.331-168G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21370656 | |||||||
| chr14:21370659 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.331-171C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21370659 | |||||||
| chr14:21370687 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.331-199A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21370687 | |||||||
| chr14:21370904 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.331-416G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21370904 | |||||||
| chr14:21371106 | C | T | 1 | a0001c0002t0002g0055 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.331-618G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21371106 | |||||||
| chr14:21371118 | C | T | 1 | a0001c0001t0003g0171 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.331-630G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21371118 | |||||||
| chr14:21371206 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.330+668A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21371206 | |||||||
| chr14:21371275 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.330+599C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21371275 | |||||||
| chr14:21371320 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.330+554C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21371320 | |||||||
| chr14:21371406 | C | T | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+468G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21371406 | |||||||
| chr14:21371506 | G | C | 1 | a0001c0002t0002g0042 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.330+368C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21371506 | |||||||
| chr14:21371662 | A | G | 1 | a0002c0010t0007g0041 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.330+212T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21371662 | |||||||
| chr14:21371759 | A | T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0118 a0001c0001t0001g0128 |
3 | HG02723.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.330+115T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21371759 | |||||||
| chr14:21371773 | T | C | 1 | a0001c0001t0003g0176 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.330+101A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 3/25 | chr14 | 21371773 | |||||||
| chr14:21372072 | G | A | 2 | a0001c0007t0008g0076 a0001c0007t0008g0077 |
2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.160-28C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 2/25 | chr14 | 21372072 | |||||||
| chr14:21372087 | A | G | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-43T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 2/25 | chr14 | 21372087 | |||||||
| chr14:21372232 | C | T | 4 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0080 others(1): Show |
5 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-188G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 2/25 | chr14 | 21372232 | |||||||
| chr14:21372349 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0101 others(2): Show |
8 | HG01884.hp1 HG01891.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-305C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 2/25 | chr14 | 21372349 | |||||||
| chr14:21372514 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.160-470A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 2/25 | chr14 | 21372514 | |||||||
| chr14:21372543 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.160-499G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 2/25 | chr14 | 21372543 | |||||||
| chr14:21372751 | C | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0093 a0001c0001t0001g0200 others(4): Show |
13 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.159+587G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 2/25 | chr14 | 21372751 | |||||||
| chr14:21372770 | G | C | 5 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0079 others(2): Show |
6 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.159+568C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 2/25 | chr14 | 21372770 | |||||||
| chr14:21372844 | T | C | 1 | a0001c0005t0001g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.159+494A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 2/25 | chr14 | 21372844 | |||||||
| chr14:21372858 | A | G | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | NA18747.hp2 NA18959.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+480T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 2/25 | chr14 | 21372858 | |||||||
| chr14:21372926 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.159+412G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 2/25 | chr14 | 21372926 | |||||||
| chr14:21372995 | G | A | 2 | a0001c0006t0001g0027 a0001c0006t0001g0028 |
4 | HG00733.hp2 HG00735.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+343C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 2/25 | chr14 | 21372995 | |||||||
| chr14:21373174 | G | C | 1 | a0001c0001t0001g0160 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.159+164C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 2/25 | chr14 | 21373174 | |||||||
| chr14:21373551 | A | G | 16 | a0001c0001t0003g0014 a0001c0001t0003g0032 a0001c0001t0003g0127 others(13): Show |
20 | HG00438.hp1 NA18940.hp1 NA18943.hp2 others(17): Show |
intron_variant | MODIFIER | c.67-121T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21373551 | |||||||
| chr14:21373670 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.67-240T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21373670 | |||||||
| chr14:21373916 | C | T | 5 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0079 others(2): Show |
6 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-486G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21373916 | |||||||
| chr14:21373980 | G | A | 1 | a0001c0004t0012g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.67-550C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21373980 | |||||||
| chr14:21373997 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.67-567C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21373997 | |||||||
| chr14:21374467 | A | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(180): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.67-1037T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21374467 | |||||||
| chr14:21374655 | C | T | 7 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 others(4): Show |
9 | HG01261.hp2 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-1225G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21374655 | |||||||
| chr14:21374721 | A | G | 2 | a0001c0007t0008g0076 a0001c0007t0008g0077 |
2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.67-1291T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21374721 | |||||||
| chr14:21374739 | G | A | 10 | a0001c0005t0001g0053 a0001c0005t0001g0054 a0001c0005t0001g0067 others(7): Show |
10 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-1309C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21374739 | |||||||
| chr14:21374809 | C | G | 1 | a0001c0001t0004g0091 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.67-1379G>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21374809 | |||||||
| chr14:21374952 | G | A | 2 | a0001c0002t0001g0066 a0001c0002t0010g0065 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.67-1522C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21374952 | |||||||
| chr14:21374996 | G | A | 1 | a0001c0004t0012g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.67-1566C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21374996 | |||||||
| chr14:21375226 | C | CTGGTCTT others(17): Show |
1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-1820_67-1797dup others(24): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21375226 | |||||||
| chr14:21375257 | G | GC | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.67-1828dupG | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21375257 | |||||||
| chr14:21375370 | CAT | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0001g0201 |
5 | HG02630.hp1 HG02818.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-1942_67-1941del others(2): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21375370 | |||||||
| chr14:21375400 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG01109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.67-1970C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21375400 | |||||||
| chr14:21375486 | A | ACAAGTCC others(5): Show |
183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(180): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.67-2057_67-2056ins others(12): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21375486 | |||||||
| chr14:21375541 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.67-2111A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21375541 | |||||||
| chr14:21375581 | G | T | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-2151C>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21375581 | |||||||
| chr14:21375610 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67-2180A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21375610 | |||||||
| chr14:21375656 | C | T | 1 | a0001c0002t0001g0015 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.67-2226G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21375656 | |||||||
| chr14:21375799 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0119 others(4): Show |
12 | HG01070.hp2 HG01071.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.67-2369C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21375799 | |||||||
| chr14:21376030 | A | G | 1 | a0001c0004t0001g0204 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-2600T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21376030 | |||||||
| chr14:21376355 | T | C | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-2925A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21376355 | |||||||
| chr14:21376381 | T | C | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-2951A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21376381 | |||||||
| chr14:21376405 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.67-2975T>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21376405 | |||||||
| chr14:21376416 | C | A | 1 | a0001c0008t0001g0047 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.67-2986G>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21376416 | |||||||
| chr14:21376454 | T | C | 1 | a0001c0002t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67-3024A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21376454 | |||||||
| chr14:21376547 | T | C | 2 | a0001c0002t0001g0066 a0001c0002t0010g0065 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.67-3117A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21376547 | |||||||
| chr14:21376564 | A | G | 8 | a0001c0001t0001g0024 a0001c0001t0001g0039 a0001c0001t0001g0085 others(5): Show |
10 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.67-3134T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21376564 | |||||||
| chr14:21377076 | GA | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(150): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.67-3647delT | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377076 | |||||||
| chr14:21377091 | A | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0084 a0001c0001t0001g0086 others(2): Show |
6 | HG02258.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-3661T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377091 | |||||||
| chr14:21377212 | T | C | 4 | a0001c0005t0001g0071 a0001c0005t0001g0072 a0001c0005t0001g0073 others(1): Show |
4 | HG02055.hp2 HG03516.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-3782A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377212 | |||||||
| chr14:21377267 | T | C | 2 | a0001c0002t0001g0066 a0001c0002t0010g0065 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.67-3837A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377267 | |||||||
| chr14:21377334 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.67-3904A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377334 | |||||||
| chr14:21377390 | T | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.67-3960A>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377390 | |||||||
| chr14:21377527 | T | C | 1 | a0002c0010t0007g0041 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.67-4097A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377527 | |||||||
| chr14:21377548 | G | A | 1 | a0001c0004t0001g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67-4118C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377548 | |||||||
| chr14:21377576 | C | CT | 8 | a0001c0001t0001g0135 a0001c0001t0003g0127 a0001c0004t0001g0040 others(5): Show |
10 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-4147dupA | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377576 | |||||||
| chr14:21377623 | TTTTA | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.67-4197_67-4194del others(4): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377623 | |||||||
| chr14:21377668 | G | T | 3 | a0001c0004t0001g0018 a0001c0004t0001g0080 a0001c0004t0001g0081 |
4 | HG02257.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-4238C>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377668 | |||||||
| chr14:21377786 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0165 |
3 | HG00639.hp1 HG01109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.67-4356C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377786 | |||||||
| chr14:21377829 | G | A | 8 | a0001c0001t0001g0019 a0001c0001t0001g0083 a0001c0001t0001g0124 others(5): Show |
9 | HG01891.hp1 HG02451.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-4399C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377829 | |||||||
| chr14:21377884 | A | G | 1 | a0001c0004t0001g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67-4454T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377884 | |||||||
| chr14:21377904 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.67-4474C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377904 | |||||||
| chr14:21377920 | G | A | 1 | a0001c0005t0001g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.67-4490C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21377920 | |||||||
| chr14:21378020 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0126 others(2): Show |
9 | NA18965.hp1 NA18971.hp1 NA18977.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-4590G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378020 | |||||||
| chr14:21378081 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4651T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378081 | |||||||
| chr14:21378085 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4655C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378085 | |||||||
| chr14:21378089 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4659T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378089 | |||||||
| chr14:21378091 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4661A>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378091 | |||||||
| chr14:21378093 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4663T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378093 | |||||||
| chr14:21378096 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4666A>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378096 | |||||||
| chr14:21378099 | C | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4669G>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378099 | |||||||
| chr14:21378100 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4670A>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378100 | |||||||
| chr14:21378101 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4671A>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378101 | |||||||
| chr14:21378102 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4672A>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378102 | |||||||
| chr14:21378104 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4674T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378104 | |||||||
| chr14:21378105 | A | T | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4675T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378105 | |||||||
| chr14:21378110 | C | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4680G>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378110 | |||||||
| chr14:21378111 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4681T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378111 | |||||||
| chr14:21378113 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4683T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378113 | |||||||
| chr14:21378114 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4684T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378114 | |||||||
| chr14:21378119 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4689T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378119 | |||||||
| chr14:21378121 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4691A>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378121 | |||||||
| chr14:21378122 | C | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4692G>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378122 | |||||||
| chr14:21378125 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4695T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378125 | |||||||
| chr14:21378155 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4725T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378155 | |||||||
| chr14:21378157 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4727G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378157 | |||||||
| chr14:21378158 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4728T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378158 | |||||||
| chr14:21378161 | A | T | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4731T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378161 | |||||||
| chr14:21378162 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4732A>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378162 | |||||||
| chr14:21378163 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4733T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378163 | |||||||
| chr14:21378167 | T | TGGGGGGT others(8): Show |
1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4738_67-4737ins others(15): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378167 | |||||||
| chr14:21378174 | T | G | 1 | a0001c0005t0001g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.67-4744A>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378174 | |||||||
| chr14:21378192 | T | C | 1 | a0001c0004t0001g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.67-4762A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378192 | |||||||
| chr14:21378193 | T | C | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-4763A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378193 | |||||||
| chr14:21378240 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.67-4810T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378240 | |||||||
| chr14:21378241 | TAAAAGAC others(28): Show |
T | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4846_67-4812del others(35): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378241 | |||||||
| chr14:21378280 | A | T | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4850T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378280 | |||||||
| chr14:21378282 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4852A>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378282 | |||||||
| chr14:21378306 | A | T | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4876T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378306 | |||||||
| chr14:21378310 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4880C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378310 | |||||||
| chr14:21378315 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4885T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378315 | |||||||
| chr14:21378320 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67-4890C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378320 | |||||||
| chr14:21378357 | A | G | 19 | a0001c0001t0003g0014 a0001c0001t0003g0032 a0001c0001t0003g0034 others(16): Show |
24 | HG00438.hp1 HG02280.hp1 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.67-4927T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378357 | |||||||
| chr14:21378829 | A | T | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+5033T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378829 | |||||||
| chr14:21378830 | C | G | 1 | a0001c0004t0001g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.66+5032G>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378830 | |||||||
| chr14:21378871 | A | C | 5 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0079 others(2): Show |
6 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+4991T>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378871 | |||||||
| chr14:21378903 | G | A | 2 | a0001c0005t0001g0071 a0001c0005t0001g0074 |
2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.66+4959C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378903 | |||||||
| chr14:21378929 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.66+4933C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21378929 | |||||||
| chr14:21379045 | G | T | 1 | a0001c0005t0001g0071 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.66+4817C>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379045 | |||||||
| chr14:21379148 | A | C | 1 | a0001c0001t0001g0097 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.66+4714T>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379148 | |||||||
| chr14:21379214 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.66+4648A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379214 | |||||||
| chr14:21379287 | T | C | 1 | a0001c0011t0001g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+4575A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379287 | |||||||
| chr14:21379366 | G | A | 1 | a0001c0004t0001g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.66+4496C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379366 | |||||||
| chr14:21379441 | G | GA | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(142): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.66+4420dupT | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379441 | |||||||
| chr14:21379496 | A | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(137): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.66+4366T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379496 | |||||||
| chr14:21379602 | C | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.66+4260G>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379602 | |||||||
| chr14:21379748 | G | C | 1 | a0001c0001t0001g0024 | 2 | HG00609.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.66+4114C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379748 | |||||||
| chr14:21379843 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.66+4019G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379843 | |||||||
| chr14:21379881 | A | AAAACAAA others(1): Show |
3 | a0001c0004t0001g0040 a0001c0004t0001g0204 a0001c0004t0012g0082 |
4 | HG01261.hp2 HG02559.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+3973_66+3980dup others(8): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379881 | |||||||
| chr14:21379881 | A | AAAACAAA others(5): Show |
1 | a0001c0004t0001g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.66+3969_66+3980dup others(12): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379881 | |||||||
| chr14:21379881 | AAAAC | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(154): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.66+3977_66+3980del others(4): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379881 | |||||||
| chr14:21379881 | AAAACAAA others(5): Show |
A | 1 | a0001c0005t0011g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.66+3969_66+3980del others(12): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379881 | |||||||
| chr14:21379909 | C | A | 4 | a0001c0005t0001g0071 a0001c0005t0001g0072 a0001c0005t0001g0073 others(1): Show |
4 | HG02055.hp2 HG03516.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+3953G>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379909 | |||||||
| chr14:21379970 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.66+3892A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21379970 | |||||||
| chr14:21380059 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.66+3803A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380059 | |||||||
| chr14:21380064 | T | C | 1 | a0002c0010t0007g0041 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.66+3798A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380064 | |||||||
| chr14:21380071 | A | C | 5 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0079 others(2): Show |
6 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+3791T>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380071 | |||||||
| chr14:21380082 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.66+3780A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380082 | |||||||
| chr14:21380208 | T | C | 2 | a0001c0007t0008g0076 a0001c0007t0008g0077 |
2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.66+3654A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380208 | |||||||
| chr14:21380296 | A | ATTTTTTT others(2): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0002c0010t0007g0041 |
7 | HG00639.hp2 HG02818.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+3557_66+3565dup others(9): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380296 | |||||||
| chr14:21380296 | A | ATTTTTTT others(3): Show |
13 | a0001c0001t0001g0020 a0001c0001t0001g0097 a0001c0001t0001g0098 others(10): Show |
14 | HG00099.hp2 HG00544.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.66+3556_66+3565dup others(10): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380296 | |||||||
| chr14:21380296 | A | ATTTTTTT others(4): Show |
101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.66+3555_66+3565dup others(11): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380296 | |||||||
| chr14:21380296 | A | ATTTTTTT others(5): Show |
33 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0025 others(30): Show |
44 | HG00438.hp2 HG01069.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.66+3554_66+3565dup others(12): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380296 | |||||||
| chr14:21380296 | A | ATTTTTTT others(6): Show |
5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
5 | HG01167.hp2 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+3553_66+3565dup others(13): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380296 | |||||||
| chr14:21380451 | G | A | 1 | a0001c0001t0001g0011 | 3 | HG02257.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.66+3411C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380451 | |||||||
| chr14:21380514 | TAA | T | 1 | a0001c0001t0001g0011 | 3 | HG02257.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.66+3346_66+3347del others(2): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380514 | |||||||
| chr14:21380515 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.66+3347T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380515 | |||||||
| chr14:21380742 | T | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.66+3120A>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380742 | |||||||
| chr14:21380967 | TG | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0001g0201 |
5 | HG02630.hp1 HG02818.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+2894delC | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21380967 | |||||||
| chr14:21381069 | A | G | 2 | a0001c0007t0008g0076 a0001c0007t0008g0077 |
2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.66+2793T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381069 | |||||||
| chr14:21381095 | C | T | 1 | a0001c0004t0001g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.66+2767G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381095 | |||||||
| chr14:21381288 | TA | T | 5 | a0001c0004t0001g0018 a0001c0004t0001g0078 a0001c0004t0001g0079 others(2): Show |
6 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+2573delT | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381288 | |||||||
| chr14:21381315 | C | A | 4 | a0001c0003t0001g0188 a0001c0003t0005g0037 a0001c0003t0005g0190 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+2547G>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381315 | |||||||
| chr14:21381451 | G | T | 2 | a0001c0007t0008g0076 a0001c0007t0008g0077 |
2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.66+2411C>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381451 | |||||||
| chr14:21381475 | G | C | 1 | a0001c0001t0001g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.66+2387C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381475 | |||||||
| chr14:21381608 | AT | A | 13 | a0001c0002t0001g0206 a0001c0002t0002g0045 a0001c0004t0001g0018 others(10): Show |
15 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.66+2253delA | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381608 | |||||||
| chr14:21381608 | ATT | A | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(147): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.66+2252_66+2253del others(2): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381608 | |||||||
| chr14:21381614 | T | A | 1 | a0001c0001t0001g0192 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.66+2248A>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381614 | |||||||
| chr14:21381671 | G | A | 1 | a0001c0001t0001g0038 | 2 | NA18980.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.66+2191C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381671 | |||||||
| chr14:21381723 | C | T | 1 | a0002c0010t0007g0041 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.66+2139G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381723 | |||||||
| chr14:21381741 | C | T | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+2121G>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381741 | |||||||
| chr14:21381773 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.66+2089A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381773 | |||||||
| chr14:21381786 | C | CT | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.66+2075dupA | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381786 | |||||||
| chr14:21381821 | A | G | 2 | a0001c0007t0008g0076 a0001c0007t0008g0077 |
2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.66+2041T>C | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381821 | |||||||
| chr14:21381841 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.66+2021A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381841 | |||||||
| chr14:21381861 | T | A | 1 | a0001c0001t0001g0200 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.66+2001A>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381861 | |||||||
| chr14:21381920 | A | T | 22 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(19): Show |
32 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.66+1942T>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21381920 | |||||||
| chr14:21382078 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.66+1784C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21382078 | |||||||
| chr14:21382219 | T | C | 4 | a0001c0001t0003g0014 a0001c0001t0003g0197 a0001c0001t0003g0198 others(1): Show |
6 | NA18943.hp2 NA18972.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+1643A>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21382219 | |||||||
| chr14:21382334 | G | T | 1 | a0001c0002t0002g0042 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.66+1528C>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21382334 | |||||||
| chr14:21382343 | G | C | 1 | a0001c0004t0012g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.66+1519C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21382343 | |||||||
| chr14:21382351 | A | C | 1 | a0001c0001t0001g0020 | 2 | HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.66+1511T>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21382351 | |||||||
| chr14:21382362 | G | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0083 |
3 | HG02976.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.66+1500C>A | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21382362 | |||||||
| chr14:21382677 | CACTG | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.66+1181_66+1184del others(4): Show |
SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21382677 | |||||||
| chr14:21383110 | T | A | 1 | a0001c0001t0001g0200 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.66+752A>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21383110 | |||||||
| chr14:21383228 | G | A | 1 | a0001c0001t0001g0039 | 2 | HG02523.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.66+634C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21383228 | |||||||
| chr14:21383505 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.66+357G>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21383505 | |||||||
| chr14:21383531 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.66+331C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21383531 | |||||||
| chr14:21383556 | G | A | 3 | a0001c0004t0001g0040 a0001c0004t0001g0203 a0001c0004t0001g0204 |
4 | HG02559.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+306C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21383556 | |||||||
| chr14:21383596 | G | C | 1 | a0001c0002t0001g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.66+266C>G | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21383596 | |||||||
| chr14:21383609 | G | A | 1 | a0002c0010t0007g0041 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.66+253C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21383609 | |||||||
| chr14:21383751 | G | A | 1 | a0001c0002t0001g0206 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.66+111C>T | SUPT16H | ENSG00000092201.10 | transcript | ENST00000216297.7 | protein_coding | 1/25 | chr14 | 21383751 |