Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51298 |
| ensemblid | ENSG00000105549.11 |
| hgncid | 13706 |
| symbol | THEG |
| name | sperm microtubule associated protein 2 |
| refseq_nuc | NM_016585.5 |
| refseq_prot | NP_057669.1 |
| ensembl_nuc | ENST00000342640.9 |
| ensembl_prot | ENSP00000340088.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 361747 |
| end | 376026 |
| strand | - |
| ver | v1.2 |
| region | chr19:361747-376026 |
| region5000 | chr19:356747-381026 |
| regionname0 | THEG_chr19_361747_376026 |
| regionname5000 | THEG_chr19_356747_381026 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 379 | 237 | 75 | 65 | 52 | 15 | 28 | 35 | THEG_chr19_356747_381026 | THEG | MGDSR others(374): Show |
chr19 | 356747 | 381026 |
| a0002 | 0/0 | 379 | 68 | 0 | 3 | 61 | 0 | 4 | 43 | THEG_chr19_356747_381026 | THEG | MGDSR others(374): Show |
chr19 | 356747 | 381026 |
| a0003 | 0/0 | 379 | 39 | 1 | 1 | 29 | 1 | 7 | 19 | THEG_chr19_356747_381026 | THEG | MGDSR others(374): Show |
chr19 | 356747 | 381026 |
| a0004 | 0/0 | 167 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | MGDSR others(162): Show |
chr19 | 356747 | 381026 |
| a0005 | 0/0 | 379 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | MGDSR others(374): Show |
chr19 | 356747 | 381026 |
| a0006 | 0/0 | 379 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | MGDSR others(374): Show |
chr19 | 356747 | 381026 |
| a0007 | 0/0 | 379 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | MGDSR others(374): Show |
chr19 | 356747 | 381026 |
| a0008 | 0/0 | 370 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | MGDSR others(365): Show |
chr19 | 356747 | 381026 |
| a0009 | 0/0 | 379 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | MGDSR others(374): Show |
chr19 | 356747 | 381026 |
| a0010 | 0/0 | 306 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | MGDSR others(301): Show |
chr19 | 356747 | 381026 |
| a0011 | 0/0 | 379 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | MGDSR others(374): Show |
chr19 | 356747 | 381026 |
| a0012 | 0/0 | 379 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | MGDSR others(374): Show |
chr19 | 356747 | 381026 |
| a0013 | 0/0 | 379 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | MGDSR others(374): Show |
chr19 | 356747 | 381026 |
| a0014 | 0/0 | 379 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | MGDSR others(374): Show |
chr19 | 356747 | 381026 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1137 | 205 | 62 | 57 | 45 | 14 | 25 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0001c0004 | 0/0 | 1137 | 21 | 11 | 7 | 0 | 1 | 2 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0001c0006 | 0/0 | 1137 | 6 | 0 | 0 | 6 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0001c0013 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0001c0017 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0001c0022 | 0/0 | 1137 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0001c0023 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0001c0028 | 0/0 | 1137 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0002c0002 | 0/0 | 1137 | 64 | 0 | 3 | 57 | 0 | 4 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0002c0007 | 0/0 | 1137 | 4 | 0 | 0 | 4 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0003c0003 | 0/0 | 1137 | 35 | 1 | 0 | 27 | 1 | 6 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0003c0010 | 0/0 | 1137 | 2 | 0 | 1 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0003c0018 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0003c0025 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0004c0005 | 0/0 | 1137 | 6 | 6 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0004c0008 | 0/0 | 1137 | 4 | 4 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0004c0014 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0004c0020 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0005c0009 | 0/0 | 1137 | 3 | 3 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0006c0011 | 0/0 | 1137 | 2 | 0 | 2 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0007c0012 | 0/0 | 1137 | 2 | 0 | 1 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0008c0027 | 0/0 | 1110 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1105): Show |
chr19 | 356747 | 381026 | ||
| a0009c0026 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0010c0015 | 0/0 | 977 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(972): Show |
chr19 | 356747 | 381026 | ||
| a0011c0021 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0012c0019 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0013c0024 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 | ||
| a0014c0016 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | ATGGG others(1132): Show |
chr19 | 356747 | 381026 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1649 | 84 | 15 | 30 | 25 | 4 | 9 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0002 | 0/1 | 1649 | 38 | 7 | 7 | 13 | 2 | 8 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0003 | 0/0 | 1611 | 27 | 1 | 11 | 5 | 5 | 5 | THEG_chr19_356747_381026 | THEG | AGACA others(1606): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0004 | 0/0 | 1649 | 9 | 9 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0005 | 0/0 | 1611 | 9 | 0 | 5 | 1 | 1 | 2 | THEG_chr19_356747_381026 | THEG | AGACA others(1606): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0006 | 0/0 | 1649 | 6 | 3 | 1 | 0 | 2 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0007 | 0/0 | 1649 | 4 | 4 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0008 | 0/0 | 1649 | 2 | 2 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0009 | 0/0 | 1649 | 3 | 3 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0010 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0011 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0012 | 0/0 | 1649 | 2 | 2 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0013 | 0/0 | 1649 | 2 | 1 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0014 | 0/0 | 1777 | 2 | 2 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1772): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0017 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0019 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0020 | 0/0 | 1649 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0024 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0025 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0026 | 0/0 | 2033 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(2028): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0027 | 0/0 | 1777 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1772): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0028 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0031 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0033 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1606): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0036 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0038 | 0/0 | 1649 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0039 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0041 | 0/0 | 1649 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0001t0042 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0004t0001 | 0/0 | 1649 | 6 | 3 | 3 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0004t0002 | 0/0 | 1649 | 5 | 3 | 0 | 0 | 0 | 2 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0004t0003 | 0/0 | 1611 | 5 | 0 | 4 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1606): Show |
chr19 | 356747 | 381026 |
| a0001c0004t0004 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0004t0007 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0004t0016 | 0/0 | 2033 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(2028): Show |
chr19 | 356747 | 381026 |
| a0001c0004t0022 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0004t0034 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0006t0001 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0006t0002 | 0/0 | 1649 | 3 | 0 | 0 | 3 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0006t0003 | 0/0 | 1611 | 2 | 0 | 0 | 2 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1606): Show |
chr19 | 356747 | 381026 |
| a0001c0013t0001 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0017t0001 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0022t0001 | 0/0 | 1649 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0023t0030 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0001c0028t0001 | 0/0 | 1649 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0002c0002t0001 | 0/0 | 1649 | 47 | 0 | 2 | 42 | 0 | 3 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0002c0002t0002 | 0/0 | 1649 | 11 | 0 | 1 | 9 | 0 | 1 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0002c0002t0003 | 0/0 | 1611 | 4 | 0 | 0 | 4 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1606): Show |
chr19 | 356747 | 381026 |
| a0002c0002t0037 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0002c0002t0043 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0002c0007t0001 | 0/0 | 1649 | 2 | 0 | 0 | 2 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0002c0007t0005 | 0/0 | 1611 | 2 | 0 | 0 | 2 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1606): Show |
chr19 | 356747 | 381026 |
| a0003c0003t0001 | 0/0 | 1649 | 28 | 1 | 0 | 24 | 0 | 3 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0003c0003t0002 | 0/0 | 1649 | 3 | 0 | 0 | 1 | 0 | 2 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0003c0003t0015 | 0/0 | 1713 | 2 | 0 | 0 | 2 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1708): Show |
chr19 | 356747 | 381026 |
| a0003c0003t0023 | 0/0 | 1649 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0003c0003t0045 | 0/0 | 1649 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0003c0010t0002 | 0/0 | 1649 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0003c0010t0044 | 0/0 | 1649 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0003c0018t0001 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0003c0025t0001 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0004c0005t0002 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0004c0005t0010 | 0/0 | 1649 | 2 | 2 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0004c0005t0011 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0004c0005t0018 | 0/0 | 1777 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1772): Show |
chr19 | 356747 | 381026 |
| a0004c0005t0035 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0004c0008t0001 | 0/0 | 1649 | 2 | 2 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0004c0008t0004 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0004c0008t0006 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0004c0014t0021 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0004c0020t0002 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0005c0009t0008 | 0/0 | 1649 | 2 | 2 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0005c0009t0029 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0006c0011t0001 | 0/0 | 1649 | 2 | 0 | 2 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0007c0012t0003 | 0/0 | 1611 | 2 | 0 | 1 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | AGACA others(1606): Show |
chr19 | 356747 | 381026 |
| a0008c0027t0001 | 0/0 | 1622 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1617): Show |
chr19 | 356747 | 381026 |
| a0009c0026t0001 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0010c0015t0003 | 0/0 | 1451 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1446): Show |
chr19 | 356747 | 381026 |
| a0011c0021t0002 | 0/0 | 1649 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0012c0019t0001 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0013c0024t0040 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| a0014c0016t0032 | 0/0 | 1649 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | AGACA others(1644): Show |
chr19 | 356747 | 381026 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0306 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0005g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0010g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0012g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0012g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0013g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0014g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0017g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0019g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0020g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0024g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0025g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0026g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0027g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0028g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0031g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0033g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0036g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0038g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0039g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0041g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0001t0042g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0003g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0016g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0022g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0004t0034g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0006t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0006t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0006t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0006t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0006t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0006t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0013t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0017t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0022t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0023t0030g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0001c0028t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0037g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0002t0043g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0007t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0007t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0007t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0002c0007t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0015g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0015g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0023g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0003t0045g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0010t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0010t0044g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0018t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0003c0025t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0004c0005t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0004c0005t0010g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0004c0005t0011g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0004c0005t0018g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0004c0005t0035g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0004c0008t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0004c0008t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0004c0008t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0004c0008t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0004c0014t0021g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0004c0020t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0005c0009t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0005c0009t0008g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0005c0009t0029g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0006c0011t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0007c0012t0003g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0007c0012t0003g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0008c0027t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0009c0026t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0010c0015t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0011c0021t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0012c0019t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0013c0024t0040g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| a0014c0016t0032g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0192 | EUR | GBR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0208 | EUR | GBR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0064 | EUR | GBR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00140 | hp2 | a0001 | c0004 | t0003 | g0134 | EUR | GBR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | FIN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0098 | EUR | FIN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0233 | EUR | FIN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | FIN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00423 | hp2 | a0003 | c0003 | t0001 | g0022 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00438 | hp1 | a0001 | c0006 | t0003 | g0324 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00438 | hp2 | a0003 | c0003 | t0001 | g0262 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00544 | hp1 | a0002 | c0002 | t0037 | g0180 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00558 | hp1 | a0003 | c0003 | t0001 | g0247 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0327 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00609 | hp2 | a0003 | c0003 | t0001 | g0331 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00621 | hp1 | a0003 | c0018 | t0001 | g0252 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0323 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | CHS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00733 | hp2 | a0008 | c0027 | t0001 | g0216 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0103 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01069 | hp1 | a0001 | c0004 | t0003 | g0009 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01071 | hp1 | a0001 | c0004 | t0003 | g0009 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0080 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01106 | hp2 | a0001 | c0004 | t0003 | g0136 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01167 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01168 | hp2 | a0006 | c0011 | t0001 | g0025 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01169 | hp1 | a0006 | c0011 | t0001 | g0025 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01169 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01192 | hp1 | a0007 | c0012 | t0003 | g0337 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01243 | hp1 | a0001 | c0004 | t0001 | g0133 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01243 | hp2 | a0001 | c0001 | t0013 | g0014 | AMR | PUR | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0063 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01358 | hp1 | a0001 | c0022 | t0001 | g0224 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01433 | hp1 | a0001 | c0001 | t0038 | g0205 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0294 | EUR | IBS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01515 | hp2 | a0003 | c0003 | t0023 | g0055 | EUR | IBS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0221 | EUR | IBS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0227 | EUR | IBS | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01884 | hp1 | a0001 | c0004 | t0022 | g0032 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01884 | hp2 | a0001 | c0001 | t0019 | g0047 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0120 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01891 | hp2 | a0001 | c0004 | t0002 | g0042 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01934 | hp1 | a0001 | c0004 | t0003 | g0135 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0302 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01952 | hp1 | a0001 | c0001 | t0020 | g0086 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0085 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02040 | hp1 | a0003 | c0003 | t0001 | g0206 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02055 | hp1 | a0005 | c0009 | t0008 | g0124 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02055 | hp2 | a0001 | c0004 | t0016 | g0044 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0314 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02056 | hp2 | a0001 | c0006 | t0002 | g0108 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02071 | hp1 | a0003 | c0003 | t0001 | g0282 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02074 | hp1 | a0001 | c0006 | t0001 | g0321 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02080 | hp1 | a0002 | c0002 | t0003 | g0304 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02083 | hp1 | a0009 | c0026 | t0001 | g0250 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0309 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0051 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02135 | hp1 | a0003 | c0003 | t0001 | g0241 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02145 | hp1 | a0001 | c0001 | t0039 | g0168 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02145 | hp2 | a0004 | c0014 | t0021 | g0036 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02148 | hp2 | a0010 | c0015 | t0003 | g0137 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CDX | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CDX | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0129 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0057 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02258 | hp2 | a0001 | c0001 | t0036 | g0149 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0260 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02280 | hp2 | a0001 | c0001 | t0025 | g0117 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0111 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02451 | hp2 | a0001 | c0004 | t0002 | g0039 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0316 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | KHV | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02572 | hp1 | a0011 | c0021 | t0002 | g0058 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02572 | hp2 | a0001 | c0004 | t0034 | g0132 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0066 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02622 | hp1 | a0004 | c0008 | t0001 | g0161 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02622 | hp2 | a0001 | c0001 | t0014 | g0012 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02630 | hp1 | a0001 | c0001 | t0014 | g0012 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0087 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0265 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02698 | hp1 | a0001 | c0028 | t0001 | g0336 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0303 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0090 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0218 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02818 | hp1 | a0004 | c0005 | t0035 | g0145 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02818 | hp2 | a0001 | c0001 | t0027 | g0119 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02886 | hp1 | a0004 | c0005 | t0010 | g0011 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0273 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02895 | hp2 | a0001 | c0001 | t0042 | g0296 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0147 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | ESN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0146 | AFR | ESN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02965 | hp1 | a0005 | c0009 | t0008 | g0123 | AFR | ESN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02970 | hp1 | a0004 | c0005 | t0002 | g0035 | AFR | ESN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02970 | hp2 | a0001 | c0001 | t0028 | g0130 | AFR | ESN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0230 | AFR | ESN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0204 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0109 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03098 | hp1 | a0004 | c0005 | t0010 | g0011 | AFR | MSL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03098 | hp2 | a0001 | c0004 | t0002 | g0043 | AFR | MSL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03130 | hp1 | a0004 | c0020 | t0002 | g0048 | AFR | ESN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | ESN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03139 | hp2 | a0001 | c0001 | t0031 | g0251 | AFR | ESN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03195 | hp2 | a0001 | c0004 | t0007 | g0040 | AFR | ESN | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0131 | AFR | MSL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0110 | AFR | MSL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0118 | AFR | MSL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0020 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03453 | hp1 | a0001 | c0023 | t0030 | g0126 | AFR | MSL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0139 | AFR | MSL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03492 | hp1 | a0003 | c0003 | t0045 | g0162 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0102 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03540 | hp2 | a0004 | c0008 | t0006 | g0297 | AFR | GWD | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0128 | AFR | MSL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03579 | hp2 | a0005 | c0009 | t0029 | g0125 | AFR | MSL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03669 | hp1 | a0003 | c0010 | t0002 | g0031 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0287 | SAS | STU | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0284 | SAS | STU | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0237 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03710 | hp1 | a0003 | c0003 | t0002 | g0069 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03710 | hp2 | a0007 | c0012 | t0003 | g0338 | SAS | PJL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0313 | SAS | BEB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0191 | SAS | BEB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03942 | hp1 | a0001 | c0004 | t0002 | g0034 | SAS | BEB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0088 | SAS | BEB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | STU | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | STU | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | BEB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | BEB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG04199 | hp1 | a0001 | c0001 | t0041 | g0219 | SAS | STU | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG04199 | hp2 | a0001 | c0004 | t0002 | g0033 | SAS | STU | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG04204 | hp1 | a0003 | c0003 | t0002 | g0097 | SAS | STU | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0076 | SAS | STU | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18522 | hp1 | a0001 | c0004 | t0004 | g0038 | AFR | YRI | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18522 | hp2 | a0004 | c0005 | t0018 | g0041 | AFR | YRI | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18612 | hp2 | a0003 | c0003 | t0001 | g0200 | EAS | CHB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | CHB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | CHB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0127 | AFR | YRI | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18942 | hp1 | a0002 | c0007 | t0001 | g0142 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18942 | hp2 | a0001 | c0017 | t0001 | g0141 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18943 | hp1 | a0003 | c0003 | t0001 | g0022 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18948 | hp1 | a0001 | c0006 | t0003 | g0322 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18950 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0231 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18953 | hp2 | a0003 | c0003 | t0001 | g0332 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18963 | hp2 | a0012 | c0019 | t0001 | g0160 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0311 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18964 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18965 | hp1 | a0002 | c0002 | t0003 | g0016 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18969 | hp1 | a0003 | c0025 | t0001 | g0190 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0325 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18983 | hp1 | a0002 | c0007 | t0005 | g0029 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18990 | hp1 | a0002 | c0002 | t0003 | g0185 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18990 | hp2 | a0013 | c0024 | t0040 | g0318 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18994 | hp1 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18994 | hp2 | a0001 | c0006 | t0002 | g0083 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18999 | hp1 | a0002 | c0002 | t0043 | g0272 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19002 | hp1 | a0003 | c0003 | t0001 | g0279 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19002 | hp2 | a0014 | c0016 | t0032 | g0140 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19003 | hp1 | a0003 | c0003 | t0001 | g0229 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0028 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19004 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19004 | hp2 | a0003 | c0003 | t0002 | g0113 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19005 | hp1 | a0001 | c0006 | t0002 | g0065 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19009 | hp1 | a0001 | c0001 | t0017 | g0067 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19030 | hp1 | a0001 | c0001 | t0026 | g0122 | AFR | LWK | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19030 | hp2 | a0001 | c0001 | t0013 | g0014 | AFR | LWK | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19068 | hp1 | a0003 | c0003 | t0015 | g0157 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19078 | hp2 | a0003 | c0003 | t0001 | g0264 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19085 | hp2 | a0002 | c0007 | t0001 | g0143 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19086 | hp1 | a0003 | c0003 | t0001 | g0028 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19086 | hp2 | a0002 | c0007 | t0005 | g0030 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19087 | hp1 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0320 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19089 | hp2 | a0002 | c0002 | t0003 | g0016 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19090 | hp1 | a0003 | c0003 | t0015 | g0244 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | YRI | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA19240 | hp2 | a0004 | c0008 | t0004 | g0114 | AFR | YRI | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ASW | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | ASW | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | TSI | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | TSI | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0197 | EUR | TSI | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0093 | EUR | TSI | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | GIH | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | GIH | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0159 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG01123 | hp2 | a0003 | c0010 | t0044 | g0138 | AMR | CLM | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02486 | hp1 | a0001 | c0001 | t0024 | g0116 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0121 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0169 | AFR | ACB | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03471 | hp1 | a0001 | c0013 | t0001 | g0144 | AFR | MSL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG03471 | hp2 | a0004 | c0005 | t0011 | g0037 | AFR | MSL | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG06807 | hp1 | a0004 | c0008 | t0001 | g0298 | AFR | USA | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | USA | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | USA | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA20300 | hp2 | a0001 | c0001 | t0011 | g0059 | AFR | USA | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA21309 | hp1 | a0001 | c0001 | t0033 | g0299 | AFR | LWK | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | LWK | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0079 | REF | REF | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0306 | REF | REF | THEG_chr19_356747_381026 | THEG | chr19 | 356747 | 381026 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:361747 | C | CGACGGTC others(441): Show |
1 | a0001 | 1 | HG03579.hp1 | splice_region_variant | LOW | c.*452_*453insAGAGTC others(442): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | chr19 | 361747 | |||||||
| chr19:361747 | C | CGACGGTC others(185): Show |
1 | a0001 | 3 | HG02486.hp1 HG02717.hp2 HG03225.hp1 |
splice_region_variant | LOW | c.*452_*453insAGAGTC others(186): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | chr19 | 361747 | |||||||
| chr19:361747 | C | CGACGGTC others(121): Show |
1 | a0001 | 3 | HG02258.hp1 HG03139.hp2 HG03540.hp1 |
splice_region_variant | LOW | c.*452_*453insAGAGTC others(122): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | chr19 | 361747 | |||||||
| chr19:361747 | C | T | 4 | a0001 a0003 a0004 others(1): Show |
23 | HG00099.hp1 HG01123.hp1 HG01516.hp1 others(20): Show |
splice_region_variant | LOW | c.*453G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | chr19 | 361747 | |||||||
| chr19:362249 | G | T | 1 | a0014 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.1091C>A | p.Pro364His | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 1147/1649 | 1091/1140 | 364/379 | chr19 | 362249 | |||
| chr19:362283 | C | T | 3 | a0003 a0004 a0009 |
41 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(38): Show |
missense_variant | MODERATE | c.1057G>A | p.Asp353Asn | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 1113/1649 | 1057/1140 | 353/379 | chr19 | 362283 | |||
| chr19:363143 | AACCCTGT others(7082): Show |
A | 1 | a0010 | 1 | HG02148.hp2 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.753+973_914-718del | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/8 | chr19 | 363143 | |||||||
| chr19:367083 | G | A | 1 | a0001 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.895C>T | p.Arg299Cys | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/8 | 951/1649 | 895/1140 | 299/379 | chr19 | 367083 | |||
| chr19:367089 | G | A | 4 | a0001 a0003 a0004 others(1): Show |
24 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(21): Show |
missense_variant | MODERATE | c.889C>T | p.His297Tyr | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/8 | 945/1649 | 889/1140 | 297/379 | chr19 | 367089 | |||
| chr19:367178 | C | T | 3 | a0001 a0002 a0003 |
13 | HG02040.hp1 HG02071.hp1 HG02129.hp1 others(10): Show |
missense_variant | MODERATE | c.800G>A | p.Arg267Gln | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/8 | 856/1649 | 800/1140 | 267/379 | chr19 | 367178 | |||
| chr19:371213 | T | C | 1 | a0013 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.745A>G | p.Met249Val | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/8 | 801/1649 | 745/1140 | 249/379 | chr19 | 371213 | |||
| chr19:371266 | C | T | 1 | a0011 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.692G>A | p.Arg231His | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/8 | 748/1649 | 692/1140 | 231/379 | chr19 | 371266 | |||
| chr19:372661 | C | A | 3 | a0002 a0004 a0009 |
70 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(67): Show |
missense_variant | MODERATE | c.605G>T | p.Arg202Ile | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/8 | 661/1649 | 605/1140 | 202/379 | chr19 | 372661 | |||
| chr19:372689 | G | A | 1 | a0006 | 2 | HG01168.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.577C>T | p.Arg193Cys | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/8 | 633/1649 | 577/1140 | 193/379 | chr19 | 372689 | |||
| chr19:373531 | C | T | 1 | a0004 | 12 | HG02145.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
stop_gained&splice_region_variant | HIGH | c.504G>A | p.Trp168* | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/8 | 560/1649 | 504/1140 | 168/379 | chr19 | 373531 | |||
| chr19:373944 | A | G | 1 | a0012 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.499T>C | p.Cys167Arg | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 3/8 | 555/1649 | 499/1140 | 167/379 | chr19 | 373944 | |||
| chr19:374299 | CTGTCTTT others(20): Show |
C | 1 | a0008 | 1 | HG00733.hp2 | disruptive_inframe_deletion&splice_region_variant | MODERATE | c.404_430delAGATAAAC others(19): Show |
p.Lys135_Asp143del | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 2/8 | 486/1649 | 404/1140 | 135/379 | chr19 | 374299 | |||
| chr19:375735 | T | C | 1 | a0007 | 2 | HG01192.hp1 HG03710.hp2 |
missense_variant | MODERATE | c.236A>G | p.Asp79Gly | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/8 | 292/1649 | 236/1140 | 79/379 | chr19 | 375735 | |||
| chr19:375855 | C | T | 1 | a0005 | 3 | HG02055.hp1 HG02965.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.116G>A | p.Ser39Asn | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/8 | 172/1649 | 116/1140 | 39/379 | chr19 | 375855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:362338 | G | A | 1 | a0001c0022 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.1002C>T | p.Pro334Pro | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 1058/1649 | 1002/1140 | 334/379 | chr19 | 362338 | |||
| chr19:362401 | G | A | 1 | a0001c0023 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.939C>T | p.Cys313Cys | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 995/1649 | 939/1140 | 313/379 | chr19 | 362401 | |||
| chr19:371250 | G | A | 4 | a0001c0006 a0001c0017 a0003c0025 others(1): Show |
9 | HG00438.hp1 HG02056.hp2 HG02074.hp1 others(6): Show |
synonymous_variant | LOW | c.708C>T | p.Ala236Ala | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/8 | 764/1649 | 708/1140 | 236/379 | chr19 | 371250 | |||
| chr19:373990 | C | T | 1 | a0001c0013 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.453G>A | p.Gly151Gly | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 3/8 | 509/1649 | 453/1140 | 151/379 | chr19 | 373990 | |||
| chr19:373996 | A | G | 1 | a0003c0018 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.447T>C | p.Gly149Gly | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 3/8 | 503/1649 | 447/1140 | 149/379 | chr19 | 373996 | |||
| chr19:375668 | T | C | 1 | a0001c0028 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.303A>G | p.Glu101Glu | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/8 | 359/1649 | 303/1140 | 101/379 | chr19 | 375668 | |||
| chr19:375779 | A | G | 9 | a0001c0004 a0001c0013 a0001c0017 others(6): Show |
38 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(35): Show |
synonymous_variant | LOW | c.192T>C | p.Leu64Leu | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/8 | 248/1649 | 192/1140 | 64/379 | chr19 | 375779 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:361750 | C | T | 1 | a0003c0003t0015 | 2 | NA19068.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*450G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 450 | chr19 | 361750 | ||||||
| chr19:361751 | G | A | 9 | a0001c0001t0001 a0003c0003t0001 a0003c0003t0002 others(6): Show |
39 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*449C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 449 | chr19 | 361751 | ||||||
| chr19:361761 | G | C | 16 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(13): Show |
21 | HG01123.hp2 HG01243.hp2 HG01515.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*439C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 439 | chr19 | 361761 | ||||||
| chr19:361761 | G | GCCCTCAG others(121): Show |
1 | a0004c0005t0002 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*311_*438dupGCCACG others(122): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 438 | chr19 | 361761 | ||||||
| chr19:361761 | G | GCCCTCAG others(505): Show |
1 | a0001c0004t0001 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*438_*439insGCCACG others(506): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 438 | chr19 | 361761 | ||||||
| chr19:361761 | G | GCCCTCAG others(313): Show |
1 | a0001c0001t0001 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*438_*439insGCCACG others(314): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 438 | chr19 | 361761 | ||||||
| chr19:361761 | G | GCCCTCAG others(505): Show |
2 | a0001c0001t0001 a0001c0001t0002 |
3 | HG00738.hp1 HG01978.hp1 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*438_*439insGCCACG others(506): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 438 | chr19 | 361761 | ||||||
| chr19:361763 | C | CCTCAGGA others(121): Show |
1 | a0004c0005t0035 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436_*437insAGCCCA others(122): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 436 | chr19 | 361763 | ||||||
| chr19:361763 | C | T | 8 | a0001c0001t0004 a0001c0001t0006 a0001c0004t0004 others(5): Show |
22 | HG00099.hp1 HG01123.hp1 HG01516.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*437G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 437 | chr19 | 361763 | ||||||
| chr19:361769 | C | G | 14 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0008 others(11): Show |
49 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*431G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 431 | chr19 | 361769 | ||||||
| chr19:361776 | G | A | 9 | a0001c0001t0004 a0001c0001t0006 a0001c0004t0004 others(6): Show |
23 | HG00099.hp1 HG01123.hp1 HG01516.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*424C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 424 | chr19 | 361776 | ||||||
| chr19:361779 | G | A | 10 | a0001c0001t0004 a0001c0001t0006 a0001c0004t0004 others(7): Show |
24 | HG00099.hp1 HG01123.hp1 HG01516.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*421C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 421 | chr19 | 361779 | ||||||
| chr19:361784 | C | CTTTGACT others(377): Show |
1 | a0001c0004t0002 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*415_*416insCCAGCC others(378): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 415 | chr19 | 361784 | ||||||
| chr19:361784 | C | CTTTGACT others(57): Show |
3 | a0001c0001t0001 a0001c0006t0002 a0002c0002t0002 |
3 | HG02129.hp2 HG03017.hp1 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*352_*415dupCCAGCC others(58): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 415 | chr19 | 361784 | ||||||
| chr19:361784 | C | CTTTGACT others(441): Show |
1 | a0001c0001t0002 | 2 | HG02809.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*415_*416insCCAGCC others(442): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 415 | chr19 | 361784 | ||||||
| chr19:361784 | C | CTTTGACT others(121): Show |
8 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(5): Show |
13 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*288_*415dupCCAGCC others(122): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 415 | chr19 | 361784 | ||||||
| chr19:361784 | C | G | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(33): Show |
91 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*416G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 416 | chr19 | 361784 | ||||||
| chr19:361798 | G | A | 1 | a0001c0023t0030 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 402 | chr19 | 361798 | ||||||
| chr19:361806 | G | A | 1 | a0013c0024t0040 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*394C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 394 | chr19 | 361806 | ||||||
| chr19:361806 | G | T | 14 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(11): Show |
29 | HG00099.hp1 HG01123.hp1 HG01243.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*394C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 394 | chr19 | 361806 | ||||||
| chr19:361811 | C | T | 7 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0024 others(4): Show |
11 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*389G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 389 | chr19 | 361811 | ||||||
| chr19:361825 | C | G | 10 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0017 others(7): Show |
14 | HG00544.hp1 HG01884.hp2 HG02257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*375G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 375 | chr19 | 361825 | ||||||
| chr19:361827 | C | CCTCAGCA others(377): Show |
2 | a0001c0001t0026 a0001c0004t0016 |
2 | HG02055.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*372_*373insAGCCCA others(378): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 372 | chr19 | 361827 | ||||||
| chr19:361827 | C | T | 7 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0019 others(4): Show |
11 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*373G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 373 | chr19 | 361827 | ||||||
| chr19:361833 | C | G | 1 | a0001c0001t0036 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*367G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 367 | chr19 | 361833 | ||||||
| chr19:361840 | G | A | 3 | a0001c0001t0013 a0001c0001t0036 a0001c0004t0022 |
4 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*360C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 360 | chr19 | 361840 | ||||||
| chr19:361843 | G | A | 1 | a0001c0001t0036 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*357C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 357 | chr19 | 361843 | ||||||
| chr19:361848 | G | C | 1 | a0001c0001t0041 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 352 | chr19 | 361848 | ||||||
| chr19:361875 | C | T | 2 | a0001c0001t0019 a0001c0001t0042 |
2 | HG01884.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*325G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 325 | chr19 | 361875 | ||||||
| chr19:361889 | C | G | 1 | a0001c0001t0036 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*311G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 311 | chr19 | 361889 | ||||||
| chr19:361897 | C | G | 1 | a0001c0001t0036 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*303G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 303 | chr19 | 361897 | ||||||
| chr19:361904 | G | A | 19 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(16): Show |
34 | HG00099.hp1 HG01123.hp1 HG01243.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*296C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 296 | chr19 | 361904 | ||||||
| chr19:361907 | G | A | 17 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(14): Show |
32 | HG00099.hp1 HG01123.hp1 HG01243.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*293C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 293 | chr19 | 361907 | ||||||
| chr19:361912 | G | C | 3 | a0001c0001t0019 a0001c0001t0042 a0002c0002t0043 |
3 | HG01884.hp2 HG02895.hp2 NA18999.hp1 |
3_prime_UTR_variant | MODIFIER | c.*288C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 288 | chr19 | 361912 | ||||||
| chr19:361929 | G | A | 16 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(13): Show |
31 | HG00099.hp1 HG01123.hp1 HG01123.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*271C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 271 | chr19 | 361929 | ||||||
| chr19:361933 | C | T | 18 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(15): Show |
33 | HG00099.hp1 HG01123.hp1 HG01123.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*267G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 267 | chr19 | 361933 | ||||||
| chr19:361939 | C | T | 26 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(23): Show |
45 | HG00099.hp1 HG01123.hp1 HG01123.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*261G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 261 | chr19 | 361939 | ||||||
| chr19:361942 | C | CGGTCCCG others(57): Show |
1 | a0003c0003t0015 | 2 | NA19068.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*257_*258insATCAGA others(58): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 257 | chr19 | 361942 | ||||||
| chr19:361942 | C | T | 19 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(16): Show |
34 | HG00099.hp1 HG01123.hp1 HG01123.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*258G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 258 | chr19 | 361942 | ||||||
| chr19:362001 | G | C | 1 | a0001c0001t0020 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*199C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 199 | chr19 | 362001 | ||||||
| chr19:362009 | T | C | 1 | a0004c0014t0021 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 191 | chr19 | 362009 | ||||||
| chr19:362028 | G | T | 1 | a0014c0016t0032 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*172C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 172 | chr19 | 362028 | ||||||
| chr19:362030 | A | G | 1 | a0001c0004t0022 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*170T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 170 | chr19 | 362030 | ||||||
| chr19:362108 | T | C | 5 | a0001c0004t0022 a0001c0023t0030 a0003c0003t0015 others(2): Show |
6 | HG01123.hp2 HG01515.hp2 HG01884.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*92A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 92 | chr19 | 362108 | ||||||
| chr19:362144 | A | G | 7 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0024 others(4): Show |
11 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*56T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 56 | chr19 | 362144 | ||||||
| chr19:362173 | T | C | 1 | a0003c0003t0045 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*27A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 8/8 | 27 | chr19 | 362173 | ||||||
| chr19:375976 | G | A | 2 | a0001c0001t0024 a0001c0001t0025 |
2 | HG02280.hp2 HG02486.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-6C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/8 | chr19 | 375976 | |||||||
| chr19:375994 | G | A | 3 | a0001c0001t0009 a0001c0001t0026 a0001c0001t0027 |
5 | HG01891.hp1 HG02486.hp2 HG02818.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-24C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/8 | 24 | chr19 | 375994 | ||||||
| chr19:375996 | G | A | 6 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0028 others(3): Show |
9 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-26C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/8 | chr19 | 375996 | |||||||
| chr19:376008 | C | T | 37 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(34): Show |
116 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(113): Show |
5_prime_UTR_variant | MODIFIER | c.-38G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/8 | 38 | chr19 | 376008 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:362432 | G | C | 34 | a0003c0003t0001g0003 a0003c0003t0001g0022 a0003c0003t0001g0027 others(31): Show |
39 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(36): Show |
splice_region_variant&intron_variant | LOW | c.914-6C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362432 | |||||||
| chr19:362635 | G | A | 1 | a0001c0001t0002g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.914-209C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362635 | |||||||
| chr19:362639 | G | T | 1 | a0001c0006t0003g0324 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.914-213C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362639 | |||||||
| chr19:362723 | G | A | 29 | a0001c0001t0004g0005 a0001c0001t0004g0056 a0001c0001t0004g0087 others(26): Show |
31 | HG00099.hp1 HG01123.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.914-297C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362723 | |||||||
| chr19:362748 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0036g0149 |
3 | HG02258.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.914-322T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362748 | |||||||
| chr19:362765 | T | TA | 35 | a0001c0001t0001g0154 a0001c0001t0001g0184 a0001c0001t0001g0211 others(32): Show |
35 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.914-340dupT | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362765 | |||||||
| chr19:362765 | T | TAA | 25 | a0001c0001t0001g0013 a0001c0001t0001g0167 a0001c0001t0001g0177 others(22): Show |
27 | HG00738.hp1 HG01192.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.914-341_914-340dup others(2): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362765 | |||||||
| chr19:362765 | TA | T | 45 | a0001c0001t0001g0152 a0001c0001t0001g0172 a0001c0001t0001g0238 others(42): Show |
49 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.914-340delT | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362765 | |||||||
| chr19:362765 | TAAAA | T | 29 | a0001c0001t0001g0026 a0001c0001t0004g0005 a0001c0001t0004g0056 others(26): Show |
32 | HG00099.hp1 HG01123.hp1 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.914-343_914-340del others(4): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362765 | |||||||
| chr19:362765 | TAAAAA | T | 8 | a0001c0001t0001g0263 a0001c0001t0008g0131 a0001c0001t0009g0118 others(5): Show |
8 | HG01123.hp2 HG01515.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.914-344_914-340del others(5): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362765 | |||||||
| chr19:362807 | C | T | 107 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0167 others(104): Show |
118 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.914-381G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362807 | |||||||
| chr19:362830 | C | T | 63 | a0001c0001t0001g0026 a0001c0001t0004g0005 a0001c0001t0004g0056 others(60): Show |
71 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.914-404G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362830 | |||||||
| chr19:362929 | C | A | 1 | a0002c0002t0001g0314 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.914-503G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362929 | |||||||
| chr19:362941 | C | T | 4 | a0001c0001t0001g0182 a0001c0001t0001g0207 a0001c0001t0002g0072 others(1): Show |
4 | HG01261.hp2 HG01433.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.914-515G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362941 | |||||||
| chr19:362969 | C | G | 25 | a0001c0001t0004g0005 a0001c0001t0004g0056 a0001c0001t0004g0087 others(22): Show |
27 | HG00099.hp1 HG01123.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.914-543G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362969 | |||||||
| chr19:362994 | T | C | 1 | a0008c0027t0001g0216 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.914-568A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 362994 | |||||||
| chr19:363044 | G | T | 16 | a0001c0001t0001g0013 a0001c0001t0001g0167 a0001c0001t0001g0177 others(13): Show |
18 | HG00738.hp1 HG01192.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.914-618C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363044 | |||||||
| chr19:363083 | G | A | 59 | a0001c0001t0001g0026 a0001c0001t0004g0005 a0001c0001t0004g0056 others(56): Show |
67 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.914-657C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363083 | |||||||
| chr19:363127 | G | A | 25 | a0001c0001t0004g0005 a0001c0001t0004g0056 a0001c0001t0004g0087 others(22): Show |
27 | HG00099.hp1 HG01123.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.914-701C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363127 | |||||||
| chr19:363213 | T | G | 107 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0167 others(104): Show |
118 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.914-787A>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363213 | |||||||
| chr19:363254 | G | A | 1 | a0002c0002t0002g0051 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.914-828C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363254 | |||||||
| chr19:363381 | C | T | 1 | a0001c0001t0006g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.914-955G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363381 | |||||||
| chr19:363382 | G | C | 29 | a0001c0001t0001g0013 a0001c0001t0001g0167 a0001c0001t0001g0177 others(26): Show |
31 | HG00738.hp1 HG00741.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.914-956C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363382 | |||||||
| chr19:363472 | C | T | 2 | a0001c0001t0036g0149 a0001c0001t0039g0168 |
2 | HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.914-1046G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363472 | |||||||
| chr19:363619 | C | T | 1 | a0001c0001t0039g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.914-1193G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363619 | |||||||
| chr19:363659 | G | A | 2 | a0001c0023t0030g0126 a0004c0005t0002g0035 |
2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.914-1233C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363659 | |||||||
| chr19:363659 | G | T | 18 | a0001c0001t0001g0261 a0001c0001t0001g0263 a0001c0001t0007g0090 others(15): Show |
19 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.914-1233C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363659 | |||||||
| chr19:363678 | C | T | 24 | a0001c0001t0001g0261 a0001c0001t0001g0263 a0001c0001t0007g0090 others(21): Show |
25 | HG01123.hp2 HG01243.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.914-1252G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363678 | |||||||
| chr19:363681 | C | A | 5 | a0002c0002t0001g0239 a0002c0002t0001g0308 a0003c0003t0015g0157 others(2): Show |
5 | HG01123.hp2 NA18983.hp2 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.914-1255G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363681 | |||||||
| chr19:363683 | G | A | 5 | a0002c0002t0001g0239 a0002c0002t0001g0308 a0003c0003t0015g0157 others(2): Show |
5 | HG01123.hp2 NA18983.hp2 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.914-1257C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363683 | |||||||
| chr19:363690 | C | T | 89 | a0001c0001t0001g0013 a0001c0001t0001g0148 a0001c0001t0001g0166 others(86): Show |
98 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.914-1264G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363690 | |||||||
| chr19:363694 | C | T | 1 | a0004c0005t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.914-1268G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363694 | |||||||
| chr19:363725 | G | C | 1 | a0003c0003t0001g0282 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.914-1299C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363725 | |||||||
| chr19:363754 | C | T | 68 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0329 others(65): Show |
74 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.914-1328G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363754 | |||||||
| chr19:363772 | C | T | 16 | a0001c0001t0001g0261 a0001c0001t0007g0057 a0001c0001t0007g0090 others(13): Show |
17 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.914-1346G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363772 | |||||||
| chr19:363775 | C | T | 65 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0329 others(62): Show |
72 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.914-1349G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363775 | |||||||
| chr19:363782 | G | A | 2 | a0001c0001t0019g0047 a0001c0001t0042g0296 |
2 | HG01884.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.914-1356C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363782 | |||||||
| chr19:363787 | G | A | 16 | a0001c0001t0001g0261 a0001c0001t0007g0057 a0001c0001t0007g0090 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.914-1361C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363787 | |||||||
| chr19:363824 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.914-1398G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363824 | |||||||
| chr19:363871 | T | A | 1 | a0001c0022t0001g0224 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.914-1445A>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363871 | |||||||
| chr19:363888 | C | T | 6 | a0001c0001t0001g0335 a0001c0006t0002g0108 a0001c0017t0001g0141 others(3): Show |
6 | HG02056.hp2 HG04204.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-1462G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363888 | |||||||
| chr19:363940 | C | A | 6 | a0001c0001t0001g0189 a0002c0002t0001g0239 a0002c0002t0001g0308 others(3): Show |
6 | HG01123.hp2 NA18950.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-1514G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363940 | |||||||
| chr19:363960 | G | C | 7 | a0001c0001t0001g0189 a0001c0001t0039g0168 a0002c0002t0001g0239 others(4): Show |
7 | HG01123.hp2 HG02145.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.914-1534C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363960 | |||||||
| chr19:363998 | C | T | 2 | a0001c0001t0002g0115 a0001c0001t0008g0127 |
2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.914-1572G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363998 | |||||||
| chr19:363999 | G | A | 1 | a0001c0023t0030g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.914-1573C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 363999 | |||||||
| chr19:364005 | C | T | 7 | a0001c0001t0001g0189 a0001c0001t0039g0168 a0002c0002t0001g0239 others(4): Show |
7 | HG01123.hp2 HG02145.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.914-1579G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364005 | |||||||
| chr19:364052 | G | A | 1 | a0002c0002t0043g0272 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.914-1626C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364052 | |||||||
| chr19:364055 | T | C | 2 | a0001c0001t0002g0081 a0001c0022t0001g0224 |
2 | HG01358.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.914-1629A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364055 | |||||||
| chr19:364060 | G | A | 56 | a0001c0001t0001g0019 a0001c0001t0001g0151 a0001c0001t0001g0165 others(53): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.914-1634C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364060 | |||||||
| chr19:364066 | G | A | 7 | a0001c0001t0001g0261 a0001c0001t0002g0115 a0001c0001t0008g0127 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.914-1640C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364066 | |||||||
| chr19:364069 | C | T | 6 | a0001c0001t0002g0115 a0001c0001t0007g0102 a0001c0001t0007g0110 others(3): Show |
6 | HG02257.hp1 HG02280.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.914-1643G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364069 | |||||||
| chr19:364071 | T | C | 176 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0026 others(173): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.914-1645A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364071 | |||||||
| chr19:364090 | C | T | 6 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0002g0099 others(3): Show |
6 | HG01109.hp1 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.914-1664G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364090 | |||||||
| chr19:364102 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.914-1676C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364102 | |||||||
| chr19:364104 | C | T | 4 | a0001c0001t0001g0175 a0001c0001t0002g0068 a0001c0001t0033g0299 others(1): Show |
4 | HG00733.hp1 HG01978.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.914-1678G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364104 | |||||||
| chr19:364105 | G | A | 2 | a0001c0001t0028g0130 a0001c0004t0004g0038 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.914-1679C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364105 | |||||||
| chr19:364108 | C | T | 2 | a0001c0001t0028g0130 a0001c0004t0004g0038 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.914-1682G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364108 | |||||||
| chr19:364115 | C | T | 2 | a0001c0001t0028g0130 a0001c0004t0004g0038 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.914-1689G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364115 | |||||||
| chr19:364116 | A | G | 102 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0152 others(99): Show |
110 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.914-1690T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364116 | |||||||
| chr19:364129 | C | G | 1 | a0003c0003t0001g0247 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.914-1703G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364129 | |||||||
| chr19:364135 | C | T | 1 | a0001c0004t0003g0136 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.914-1709G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364135 | |||||||
| chr19:364139 | C | G | 1 | a0001c0001t0001g0285 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.914-1713G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364139 | |||||||
| chr19:364140 | T | C | 2 | a0001c0001t0025g0117 a0001c0001t0039g0168 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.914-1714A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364140 | |||||||
| chr19:364144 | T | C | 10 | a0001c0001t0001g0263 a0001c0001t0008g0131 a0001c0001t0009g0118 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.914-1718A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364144 | |||||||
| chr19:364145 | C | A | 189 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0019 others(186): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.914-1719G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364145 | |||||||
| chr19:364145 | C | G | 1 | a0001c0001t0011g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.914-1719G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364145 | |||||||
| chr19:364148 | A | T | 1 | a0001c0001t0039g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.914-1722T>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364148 | |||||||
| chr19:364149 | C | G | 107 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0148 others(104): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.914-1723G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364149 | |||||||
| chr19:364149 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.914-1723G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364149 | |||||||
| chr19:364150 | G | A | 1 | a0011c0021t0002g0058 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.914-1724C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364150 | |||||||
| chr19:364157 | T | C | 94 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0026 others(91): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.914-1731A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364157 | |||||||
| chr19:364161 | A | G | 170 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0026 others(167): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.914-1735T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364161 | |||||||
| chr19:364162 | T | C | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.914-1736A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364162 | |||||||
| chr19:364166 | T | C | 14 | a0001c0001t0001g0261 a0001c0001t0001g0263 a0001c0001t0008g0131 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.914-1740A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364166 | |||||||
| chr19:364175 | T | C | 1 | a0001c0001t0002g0064 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.914-1749A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364175 | |||||||
| chr19:364192 | C | T | 1 | a0001c0001t0006g0303 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.914-1766G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364192 | |||||||
| chr19:364197 | C | T | 12 | a0001c0001t0001g0165 a0001c0001t0001g0295 a0001c0001t0003g0187 others(9): Show |
12 | HG00099.hp1 HG00741.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.914-1771G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364197 | |||||||
| chr19:364201 | G | C | 20 | a0001c0001t0001g0189 a0001c0001t0003g0020 a0001c0001t0003g0021 others(17): Show |
23 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.914-1775C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364201 | |||||||
| chr19:364208 | C | A | 3 | a0001c0001t0001g0261 a0001c0001t0011g0059 a0001c0013t0001g0144 |
3 | HG02976.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.914-1782G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364208 | |||||||
| chr19:364208 | C | G | 70 | a0001c0001t0001g0019 a0001c0001t0001g0151 a0001c0001t0001g0165 others(67): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.914-1782G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364208 | |||||||
| chr19:364209 | T | C | 70 | a0001c0001t0001g0019 a0001c0001t0001g0151 a0001c0001t0001g0165 others(67): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.914-1783A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364209 | |||||||
| chr19:364230 | A | G | 1 | a0001c0001t0002g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.914-1804T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364230 | |||||||
| chr19:364241 | G | A | 4 | a0001c0001t0002g0101 a0001c0001t0003g0213 a0001c0001t0003g0214 others(1): Show |
4 | HG00741.hp2 HG01099.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.914-1815C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364241 | |||||||
| chr19:364251 | G | A | 1 | a0001c0001t0025g0117 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.914-1825C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364251 | |||||||
| chr19:364261 | C | T | 1 | a0005c0009t0008g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.914-1835G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364261 | |||||||
| chr19:364278 | A | G | 5 | a0001c0001t0012g0128 a0001c0001t0024g0116 a0001c0001t0031g0251 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.914-1852T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364278 | |||||||
| chr19:364285 | T | C | 61 | a0001c0001t0001g0026 a0001c0001t0001g0167 a0001c0001t0001g0177 others(58): Show |
64 | HG00738.hp1 HG01243.hp1 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.914-1859A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364285 | |||||||
| chr19:364292 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.914-1866C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364292 | |||||||
| chr19:364293 | C | T | 6 | a0001c0001t0001g0182 a0001c0001t0001g0193 a0001c0001t0001g0207 others(3): Show |
6 | HG00741.hp1 HG01261.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-1867G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364293 | |||||||
| chr19:364302 | G | A | 17 | a0001c0001t0001g0019 a0001c0001t0001g0148 a0001c0001t0001g0166 others(14): Show |
17 | HG00099.hp1 HG01109.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.914-1876C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364302 | |||||||
| chr19:364315 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0195 a0001c0001t0001g0220 |
3 | HG01175.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.914-1889A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364315 | |||||||
| chr19:364324 | G | A | 99 | a0001c0001t0001g0013 a0001c0001t0001g0148 a0001c0001t0001g0166 others(96): Show |
109 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.914-1898C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364324 | |||||||
| chr19:364336 | C | CA | 10 | a0001c0001t0002g0072 a0001c0001t0003g0260 a0001c0001t0007g0057 others(7): Show |
10 | HG00438.hp1 HG01433.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.914-1911dupT | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364336 | |||||||
| chr19:364336 | CA | C | 48 | a0001c0001t0001g0189 a0001c0001t0001g0238 a0001c0001t0001g0278 others(45): Show |
52 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.914-1911delT | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364336 | |||||||
| chr19:364336 | CAA | C | 59 | a0001c0001t0001g0019 a0001c0001t0001g0151 a0001c0001t0001g0165 others(56): Show |
61 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.914-1912_914-1911d others(4): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364336 | |||||||
| chr19:364353 | A | G | 25 | a0001c0001t0001g0189 a0001c0001t0001g0278 a0001c0001t0002g0115 others(22): Show |
28 | HG01123.hp2 HG01243.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.914-1927T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364353 | |||||||
| chr19:364357 | GAAAGAAA others(3): Show |
G | 1 | a0001c0001t0001g0155 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.914-1941_914-1932d others(12): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364357 | |||||||
| chr19:364387 | C | T | 191 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0026 others(188): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.914-1961G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364387 | |||||||
| chr19:364445 | A | C | 1 | a0002c0002t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.914-2019T>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364445 | |||||||
| chr19:364502 | G | A | 116 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0165 others(113): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.914-2076C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364502 | |||||||
| chr19:364515 | T | TA | 9 | a0001c0001t0001g0184 a0001c0001t0002g0115 a0001c0001t0007g0090 others(6): Show |
9 | HG02257.hp1 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.914-2090dupT | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364515 | |||||||
| chr19:364554 | C | T | 1 | a0002c0002t0001g0173 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.914-2128G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364554 | |||||||
| chr19:364626 | C | A | 83 | a0001c0001t0001g0019 a0001c0001t0001g0165 a0001c0001t0001g0194 others(80): Show |
85 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.914-2200G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364626 | |||||||
| chr19:364674 | G | C | 3 | a0001c0001t0002g0054 a0001c0006t0003g0322 a0001c0006t0003g0324 |
3 | HG00438.hp1 NA18944.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.914-2248C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364674 | |||||||
| chr19:364695 | G | T | 84 | a0001c0001t0001g0019 a0001c0001t0001g0151 a0001c0001t0001g0165 others(81): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.914-2269C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364695 | |||||||
| chr19:364741 | C | T | 49 | a0001c0001t0001g0013 a0001c0001t0001g0317 a0001c0001t0001g0329 others(46): Show |
55 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.914-2315G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364741 | |||||||
| chr19:364754 | A | AC | 26 | a0001c0001t0001g0013 a0001c0001t0001g0170 a0001c0001t0001g0195 others(23): Show |
26 | HG00438.hp2 HG00544.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.913+2310dupG | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364754 | |||||||
| chr19:364844 | G | A | 31 | a0001c0001t0001g0189 a0001c0001t0001g0266 a0001c0001t0001g0270 others(28): Show |
34 | HG02056.hp2 HG03669.hp1 HG03834.hp2 others(31): Show |
intron_variant | MODIFIER | c.913+2221C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364844 | |||||||
| chr19:364862 | G | A | 1 | a0001c0023t0030g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.913+2203C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364862 | |||||||
| chr19:364884 | C | G | 10 | a0001c0001t0001g0181 a0001c0001t0002g0092 a0001c0001t0002g0095 others(7): Show |
11 | HG01243.hp2 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.913+2181G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364884 | |||||||
| chr19:364917 | G | A | 42 | a0001c0001t0001g0181 a0001c0001t0001g0189 a0001c0001t0001g0266 others(39): Show |
46 | HG01243.hp2 HG02055.hp1 HG02056.hp2 others(43): Show |
intron_variant | MODIFIER | c.913+2148C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 364917 | |||||||
| chr19:365034 | T | C | 190 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0165 others(187): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.913+2031A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365034 | |||||||
| chr19:365076 | C | T | 1 | a0001c0001t0003g0197 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.913+1989G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365076 | |||||||
| chr19:365140 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.913+1925G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365140 | |||||||
| chr19:365168 | C | T | 135 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0165 others(132): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.913+1897G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365168 | |||||||
| chr19:365188 | T | C | 178 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0165 others(175): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.913+1877A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365188 | |||||||
| chr19:365276 | C | T | 30 | a0001c0001t0001g0189 a0001c0001t0001g0266 a0001c0001t0001g0270 others(27): Show |
33 | HG02056.hp2 HG03669.hp1 HG03834.hp2 others(30): Show |
intron_variant | MODIFIER | c.913+1789G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365276 | |||||||
| chr19:365305 | G | T | 3 | a0001c0001t0001g0253 a0001c0001t0002g0060 a0001c0001t0002g0061 |
3 | HG00738.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.913+1760C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365305 | |||||||
| chr19:365389 | A | C | 10 | a0001c0001t0001g0181 a0001c0001t0002g0092 a0001c0001t0002g0095 others(7): Show |
11 | HG01243.hp2 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.913+1676T>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365389 | |||||||
| chr19:365480 | A | G | 168 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0165 others(165): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.913+1585T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365480 | |||||||
| chr19:365491 | G | GCACAGCC others(84): Show |
3 | a0004c0008t0004g0114 a0004c0008t0006g0297 a0004c0020t0002g0048 |
3 | HG03130.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.913+1573_913+1574i others(93): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365491 | |||||||
| chr19:365537 | GCACA | G | 17 | a0001c0001t0001g0167 a0001c0001t0001g0177 a0001c0001t0001g0234 others(14): Show |
17 | HG00099.hp1 HG00738.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.913+1524_913+1527d others(6): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365537 | |||||||
| chr19:365541 | A | ACACAAAC others(134): Show |
2 | a0001c0001t0007g0057 a0004c0005t0002g0035 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.913+1523_913+1524i others(143): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365541 | |||||||
| chr19:365541 | A | ACACAGCC others(30): Show |
1 | a0001c0001t0042g0296 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.913+1523_913+1524i others(39): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365541 | |||||||
| chr19:365541 | A | ATACAGCC others(30): Show |
73 | a0001c0001t0001g0019 a0001c0001t0001g0165 a0001c0001t0001g0189 others(70): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.913+1523_913+1524i others(39): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365541 | |||||||
| chr19:365541 | A | ATACAGCC others(80): Show |
8 | a0001c0001t0001g0263 a0001c0001t0006g0303 a0001c0001t0008g0131 others(5): Show |
8 | HG01891.hp1 HG02486.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.913+1523_913+1524i others(89): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365541 | |||||||
| chr19:365541 | A | ATACAGCC others(130): Show |
1 | a0001c0001t0002g0096 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.913+1523_913+1524i others(139): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365541 | |||||||
| chr19:365541 | ACACACAC others(84): Show |
A | 2 | a0001c0001t0025g0117 a0001c0004t0001g0147 |
2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.913+1433_913+1523d others(93): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365541 | |||||||
| chr19:365542 | CACACACA others(47): Show |
C | 27 | a0001c0001t0001g0266 a0001c0001t0001g0270 a0001c0001t0001g0278 others(24): Show |
30 | HG02056.hp2 HG03669.hp1 HG03834.hp2 others(27): Show |
intron_variant | MODIFIER | c.913+1469_913+1522d others(56): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365542 | |||||||
| chr19:365546 | C | A | 14 | a0001c0001t0001g0026 a0001c0001t0001g0184 a0001c0001t0002g0115 others(11): Show |
15 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.913+1519G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365546 | |||||||
| chr19:365546 | C | T | 15 | a0001c0001t0001g0167 a0001c0001t0001g0177 a0001c0001t0001g0234 others(12): Show |
15 | HG00099.hp1 HG00738.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.913+1519G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365546 | |||||||
| chr19:365555 | ACACTCG | A | 14 | a0001c0001t0001g0167 a0001c0001t0001g0177 a0001c0001t0001g0234 others(11): Show |
14 | HG00099.hp1 HG00738.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.913+1504_913+1509d others(8): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365555 | |||||||
| chr19:365561 | G | A | 12 | a0001c0001t0001g0184 a0001c0001t0002g0096 a0001c0001t0002g0115 others(9): Show |
12 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.913+1504C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365561 | |||||||
| chr19:365561 | GCTCTTAC others(134): Show |
G | 17 | a0001c0001t0001g0013 a0001c0001t0001g0329 a0001c0001t0011g0059 others(14): Show |
19 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.913+1363_913+1503d others(2): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365561 | |||||||
| chr19:365570 | CCCA | C | 14 | a0001c0001t0001g0167 a0001c0001t0001g0177 a0001c0001t0001g0234 others(11): Show |
14 | HG00099.hp1 HG00738.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.913+1492_913+1494d others(5): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365570 | |||||||
| chr19:365579 | C | T | 14 | a0001c0001t0001g0167 a0001c0001t0001g0177 a0001c0001t0001g0234 others(11): Show |
14 | HG00099.hp1 HG00738.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.913+1486G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365579 | |||||||
| chr19:365588 | T | C | 14 | a0001c0001t0001g0167 a0001c0001t0001g0177 a0001c0001t0001g0234 others(11): Show |
14 | HG00099.hp1 HG00738.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.913+1477A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365588 | |||||||
| chr19:365595 | ATACAGCC others(80): Show |
A | 1 | a0001c0001t0001g0026 | 2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.913+1383_913+1469d others(89): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365595 | |||||||
| chr19:365596 | T | A | 1 | a0001c0001t0042g0296 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.913+1469A>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365596 | |||||||
| chr19:365596 | T | C | 87 | a0001c0001t0001g0019 a0001c0001t0001g0165 a0001c0001t0001g0167 others(84): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.913+1469A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365596 | |||||||
| chr19:365605 | A | ACACTCG | 85 | a0001c0001t0001g0019 a0001c0001t0001g0165 a0001c0001t0001g0167 others(82): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.913+1459_913+1460i others(8): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365605 | |||||||
| chr19:365614 | C | CCCA | 85 | a0001c0001t0001g0019 a0001c0001t0001g0165 a0001c0001t0001g0167 others(82): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.913+1448_913+1450d others(5): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365614 | |||||||
| chr19:365620 | T | C | 86 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0165 others(83): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.913+1445A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365620 | |||||||
| chr19:365620 | T | TAGCAAGT others(43): Show |
1 | a0001c0001t0002g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.913+1395_913+1444d others(52): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365620 | |||||||
| chr19:365620 | T | TAGCAAGT others(43): Show |
1 | a0001c0001t0002g0096 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.913+1444_913+1445i others(52): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365620 | |||||||
| chr19:365629 | C | CGAGCACA others(93): Show |
2 | a0001c0001t0004g0107 a0001c0001t0004g0109 |
2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.913+1435_913+1436i others(102): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365629 | |||||||
| chr19:365629 | C | T | 86 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0165 others(83): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.913+1436G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365629 | |||||||
| chr19:365630 | G | A | 3 | a0001c0001t0007g0057 a0001c0001t0039g0168 a0004c0005t0002g0035 |
3 | HG02145.hp1 HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.913+1435C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365630 | |||||||
| chr19:365637 | C | A | 2 | a0001c0001t0025g0117 a0001c0004t0001g0147 |
2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.913+1428G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365637 | |||||||
| chr19:365639 | C | T | 1 | a0002c0002t0001g0259 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.913+1426G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365639 | |||||||
| chr19:365652 | G | A | 30 | a0001c0001t0001g0189 a0001c0001t0001g0266 a0001c0001t0001g0270 others(27): Show |
33 | HG02056.hp2 HG03669.hp1 HG03834.hp2 others(30): Show |
intron_variant | MODIFIER | c.913+1413C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365652 | |||||||
| chr19:365652 | GCTCTTAC others(43): Show |
G | 23 | a0001c0001t0001g0181 a0001c0001t0001g0317 a0001c0001t0002g0092 others(20): Show |
25 | HG01243.hp2 HG02040.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.913+1363_913+1412d others(52): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365652 | |||||||
| chr19:365682 | G | GCACA | 19 | a0001c0001t0001g0167 a0001c0001t0001g0177 a0001c0001t0001g0234 others(16): Show |
19 | HG00099.hp1 HG00738.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.913+1379_913+1382d others(6): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365682 | |||||||
| chr19:365702 | A | G | 64 | a0001c0001t0001g0026 a0001c0001t0001g0167 a0001c0001t0001g0177 others(61): Show |
68 | HG00099.hp1 HG00738.hp1 HG01123.hp1 others(65): Show |
intron_variant | MODIFIER | c.913+1363T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365702 | |||||||
| chr19:365761 | C | T | 1 | a0001c0001t0039g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.913+1304G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365761 | |||||||
| chr19:365770 | T | C | 1 | a0001c0001t0039g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.913+1295A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365770 | |||||||
| chr19:365778 | A | C | 1 | a0001c0001t0039g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.913+1287T>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365778 | |||||||
| chr19:365789 | T | A | 1 | a0001c0001t0039g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.913+1276A>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365789 | |||||||
| chr19:365861 | C | G | 108 | a0001c0001t0001g0019 a0001c0001t0001g0165 a0001c0001t0001g0181 others(105): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.913+1204G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365861 | |||||||
| chr19:365873 | G | A | 1 | a0001c0001t0019g0047 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.913+1192C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365873 | |||||||
| chr19:365918 | G | A | 2 | a0001c0001t0033g0299 a0003c0003t0001g0265 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.913+1147C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 365918 | |||||||
| chr19:366038 | A | G | 143 | a0001c0001t0001g0019 a0001c0001t0001g0165 a0001c0001t0001g0181 others(140): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.913+1027T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366038 | |||||||
| chr19:366042 | G | A | 1 | a0001c0001t0042g0296 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.913+1023C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366042 | |||||||
| chr19:366046 | C | G | 3 | a0001c0001t0006g0303 a0004c0008t0004g0114 a0004c0008t0006g0297 |
3 | HG02717.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.913+1019G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366046 | |||||||
| chr19:366055 | G | T | 1 | a0001c0001t0001g0013 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.913+1010C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366055 | |||||||
| chr19:366151 | A | C | 1 | a0001c0001t0002g0099 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.913+914T>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366151 | |||||||
| chr19:366209 | G | A | 3 | a0001c0001t0001g0165 a0001c0004t0002g0033 a0001c0004t0002g0034 |
3 | HG02698.hp2 HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.913+856C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366209 | |||||||
| chr19:366234 | T | C | 68 | a0001c0001t0001g0181 a0001c0001t0001g0189 a0001c0001t0001g0263 others(65): Show |
73 | HG01243.hp2 HG01891.hp1 HG02040.hp1 others(70): Show |
intron_variant | MODIFIER | c.913+831A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366234 | |||||||
| chr19:366244 | C | T | 1 | a0001c0004t0003g0136 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.913+821G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366244 | |||||||
| chr19:366288 | C | A | 10 | a0001c0001t0001g0263 a0001c0001t0007g0057 a0001c0001t0008g0131 others(7): Show |
10 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.913+777G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366288 | |||||||
| chr19:366299 | T | G | 1 | a0014c0016t0032g0140 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.913+766A>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366299 | |||||||
| chr19:366300 | G | T | 1 | a0014c0016t0032g0140 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.913+765C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366300 | |||||||
| chr19:366301 | T | G | 1 | a0014c0016t0032g0140 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.913+764A>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366301 | |||||||
| chr19:366303 | C | A | 1 | a0014c0016t0032g0140 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.913+762G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366303 | |||||||
| chr19:366319 | C | T | 1 | a0001c0004t0016g0044 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.913+746G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366319 | |||||||
| chr19:366327 | A | C | 68 | a0001c0001t0001g0181 a0001c0001t0001g0189 a0001c0001t0001g0263 others(65): Show |
73 | HG01243.hp2 HG01891.hp1 HG02040.hp1 others(70): Show |
intron_variant | MODIFIER | c.913+738T>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366327 | |||||||
| chr19:366364 | G | C | 21 | a0001c0001t0001g0266 a0001c0001t0001g0278 a0001c0001t0001g0286 others(18): Show |
24 | HG02056.hp2 HG03669.hp1 NA18612.hp1 others(21): Show |
intron_variant | MODIFIER | c.913+701C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366364 | |||||||
| chr19:366408 | G | A | 10 | a0001c0001t0001g0263 a0001c0001t0007g0057 a0001c0001t0008g0131 others(7): Show |
10 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.913+657C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366408 | |||||||
| chr19:366412 | A | G | 191 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0165 others(188): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.913+653T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366412 | |||||||
| chr19:366451 | C | A | 106 | a0001c0001t0001g0019 a0001c0001t0001g0165 a0001c0001t0001g0181 others(103): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.913+614G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366451 | |||||||
| chr19:366566 | C | G | 1 | a0007c0012t0003g0337 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.913+499G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366566 | |||||||
| chr19:366591 | G | A | 1 | a0003c0003t0001g0200 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.913+474C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366591 | |||||||
| chr19:366613 | G | A | 18 | a0001c0001t0001g0013 a0001c0001t0001g0329 a0001c0001t0003g0302 others(15): Show |
21 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.913+452C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366613 | |||||||
| chr19:366680 | G | A | 47 | a0001c0001t0001g0013 a0001c0001t0001g0189 a0001c0001t0001g0266 others(44): Show |
52 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.913+385C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366680 | |||||||
| chr19:366745 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.913+320G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366745 | |||||||
| chr19:366774 | T | G | 28 | a0001c0001t0001g0013 a0001c0001t0001g0184 a0001c0001t0001g0329 others(25): Show |
31 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.913+291A>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366774 | |||||||
| chr19:366804 | C | T | 96 | a0001c0001t0001g0013 a0001c0001t0001g0167 a0001c0001t0001g0177 others(93): Show |
103 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.913+261G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366804 | |||||||
| chr19:366840 | C | A | 19 | a0001c0001t0001g0013 a0001c0001t0001g0329 a0001c0001t0003g0302 others(16): Show |
22 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.913+225G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366840 | |||||||
| chr19:366846 | T | C | 174 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0165 others(171): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.913+219A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366846 | |||||||
| chr19:366926 | C | T | 9 | a0001c0001t0001g0184 a0001c0001t0002g0115 a0001c0001t0007g0090 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.913+139G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366926 | |||||||
| chr19:366986 | G | A | 11 | a0001c0001t0001g0263 a0001c0001t0002g0046 a0001c0001t0007g0057 others(8): Show |
11 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.913+79C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 7/7 | chr19 | 366986 | |||||||
| chr19:367251 | T | G | 4 | a0001c0001t0001g0225 a0001c0001t0001g0277 a0001c0001t0002g0091 others(1): Show |
4 | HG00280.hp2 HG01106.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-27A>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 367251 | |||||||
| chr19:367313 | G | A | 175 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0165 others(172): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.754-89C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 367313 | |||||||
| chr19:367348 | G | C | 13 | a0001c0001t0001g0317 a0001c0004t0016g0044 a0002c0002t0001g0243 others(10): Show |
14 | HG02040.hp1 HG02055.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.754-124C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 367348 | |||||||
| chr19:367440 | G | A | 10 | a0001c0001t0001g0263 a0001c0001t0007g0057 a0001c0001t0008g0131 others(7): Show |
10 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.754-216C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 367440 | |||||||
| chr19:367519 | T | C | 1 | a0002c0002t0002g0001 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.754-295A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 367519 | |||||||
| chr19:367584 | A | C | 1 | a0014c0016t0032g0140 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.754-360T>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 367584 | |||||||
| chr19:367726 | C | G | 86 | a0001c0001t0001g0019 a0001c0001t0001g0165 a0001c0001t0001g0181 others(83): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.754-502G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 367726 | |||||||
| chr19:367780 | C | G | 1 | a0001c0001t0036g0149 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.754-556G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 367780 | |||||||
| chr19:367892 | A | C | 1 | a0014c0016t0032g0140 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.754-668T>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 367892 | |||||||
| chr19:367979 | A | G | 183 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0165 others(180): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.754-755T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 367979 | |||||||
| chr19:368012 | C | T | 1 | a0001c0001t0036g0149 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.754-788G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368012 | |||||||
| chr19:368030 | G | A | 37 | a0001c0001t0001g0167 a0001c0001t0001g0177 a0001c0001t0001g0189 others(34): Show |
39 | HG00738.hp1 HG01243.hp1 HG01515.hp2 others(36): Show |
intron_variant | MODIFIER | c.754-806C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368030 | |||||||
| chr19:368033 | C | T | 1 | a0001c0001t0006g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.754-809G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368033 | |||||||
| chr19:368084 | T | C | 3 | a0001c0001t0006g0303 a0004c0008t0001g0298 a0004c0008t0004g0114 |
3 | HG02717.hp1 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.754-860A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368084 | |||||||
| chr19:368102 | C | T | 4 | a0002c0002t0001g0002 a0002c0002t0001g0309 a0002c0002t0001g0313 others(1): Show |
4 | HG02083.hp2 HG02132.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-878G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368102 | |||||||
| chr19:368108 | G | T | 1 | a0001c0001t0011g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.754-884C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368108 | |||||||
| chr19:368119 | G | A | 1 | a0002c0007t0001g0142 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.754-895C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368119 | |||||||
| chr19:368376 | C | T | 1 | a0002c0002t0043g0272 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.754-1152G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368376 | |||||||
| chr19:368430 | T | C | 1 | a0002c0007t0005g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.754-1206A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368430 | |||||||
| chr19:368540 | G | A | 1 | a0004c0005t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.754-1316C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368540 | |||||||
| chr19:368580 | T | C | 1 | a0002c0002t0001g0320 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.754-1356A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368580 | |||||||
| chr19:368638 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0002g0098 |
2 | HG00280.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.754-1414G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368638 | |||||||
| chr19:368646 | C | G | 1 | a0003c0003t0001g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.754-1422G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368646 | |||||||
| chr19:368726 | A | G | 2 | a0001c0001t0011g0059 a0001c0001t0042g0296 |
2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.754-1502T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368726 | |||||||
| chr19:368812 | A | G | 62 | a0001c0001t0001g0019 a0001c0001t0001g0167 a0001c0001t0001g0177 others(59): Show |
64 | HG00738.hp1 HG01123.hp1 HG01256.hp1 others(61): Show |
intron_variant | MODIFIER | c.754-1588T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368812 | |||||||
| chr19:368949 | CAACTGCA others(19): Show |
C | 1 | a0001c0001t0004g0106 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.754-1751_754-1726d others(28): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368949 | |||||||
| chr19:368953 | T | C | 27 | a0001c0001t0001g0189 a0001c0001t0001g0270 a0001c0001t0001g0278 others(24): Show |
29 | HG02056.hp2 HG02165.hp2 HG02300.hp2 others(26): Show |
intron_variant | MODIFIER | c.754-1729A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 368953 | |||||||
| chr19:369232 | G | A | 14 | a0001c0001t0002g0092 a0001c0001t0002g0095 a0001c0001t0008g0131 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.753+1973C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369232 | |||||||
| chr19:369288 | A | G | 44 | a0001c0001t0001g0013 a0001c0001t0001g0166 a0001c0001t0001g0263 others(41): Show |
46 | HG01109.hp1 HG01192.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.753+1917T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369288 | |||||||
| chr19:369305 | G | A | 1 | a0001c0006t0003g0322 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.753+1900C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369305 | |||||||
| chr19:369365 | C | T | 2 | a0001c0001t0036g0149 a0004c0005t0002g0035 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.753+1840G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369365 | |||||||
| chr19:369491 | C | T | 7 | a0001c0001t0006g0303 a0001c0001t0008g0131 a0001c0001t0009g0120 others(4): Show |
7 | HG00609.hp1 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.753+1714G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369491 | |||||||
| chr19:369492 | G | A | 3 | a0001c0001t0036g0149 a0001c0023t0030g0126 a0004c0005t0002g0035 |
3 | HG02258.hp2 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.753+1713C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369492 | |||||||
| chr19:369526 | C | T | 66 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0166 others(63): Show |
72 | HG00544.hp2 HG01109.hp1 HG01192.hp2 others(69): Show |
intron_variant | MODIFIER | c.753+1679G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369526 | |||||||
| chr19:369527 | G | A | 2 | a0001c0001t0002g0084 a0001c0001t0002g0089 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.753+1678C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369527 | |||||||
| chr19:369556 | C | A | 1 | a0001c0001t0011g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.753+1649G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369556 | |||||||
| chr19:369565 | C | A | 1 | a0001c0001t0002g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.753+1640G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369565 | |||||||
| chr19:369604 | G | T | 5 | a0001c0001t0009g0118 a0001c0001t0039g0168 a0001c0004t0001g0133 others(2): Show |
5 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.753+1601C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369604 | |||||||
| chr19:369773 | G | A | 10 | a0001c0001t0001g0166 a0001c0001t0002g0004 a0001c0001t0002g0099 others(7): Show |
10 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.753+1432C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369773 | |||||||
| chr19:369789 | C | G | 1 | a0001c0001t0003g0163 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.753+1416G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369789 | |||||||
| chr19:369798 | C | T | 1 | a0003c0003t0001g0022 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.753+1407G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369798 | |||||||
| chr19:369982 | C | T | 2 | a0002c0002t0001g0178 a0002c0002t0001g0179 |
2 | NA18944.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.753+1223G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 369982 | |||||||
| chr19:370035 | C | T | 3 | a0001c0001t0002g0115 a0001c0001t0008g0127 a0005c0009t0029g0125 |
3 | HG02280.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.753+1170G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370035 | |||||||
| chr19:370056 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0003g0163 |
2 | HG01361.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.753+1149G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370056 | |||||||
| chr19:370075 | G | A | 1 | a0001c0004t0034g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.753+1130C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370075 | |||||||
| chr19:370117 | G | T | 1 | a0001c0004t0034g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.753+1088C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370117 | |||||||
| chr19:370148 | G | A | 1 | a0001c0006t0003g0322 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.753+1057C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370148 | |||||||
| chr19:370188 | A | G | 18 | a0001c0001t0001g0189 a0001c0001t0001g0209 a0001c0001t0001g0329 others(15): Show |
18 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.753+1017T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370188 | |||||||
| chr19:370247 | C | G | 313 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0019 others(310): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.753+958G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370247 | |||||||
| chr19:370287 | C | T | 1 | a0003c0003t0001g0206 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.753+918G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370287 | |||||||
| chr19:370347 | G | GT | 140 | a0001c0001t0001g0019 a0001c0001t0001g0152 a0001c0001t0001g0153 others(137): Show |
152 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.753+857dupA | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370347 | |||||||
| chr19:370347 | G | GTTT | 6 | a0001c0001t0001g0184 a0001c0001t0007g0090 a0001c0001t0007g0102 others(3): Show |
6 | HG02257.hp1 HG02717.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.753+855_753+857dup others(3): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370347 | |||||||
| chr19:370394 | G | T | 11 | a0001c0001t0004g0056 a0001c0001t0004g0104 a0001c0001t0006g0303 others(8): Show |
11 | HG01891.hp1 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.753+811C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370394 | |||||||
| chr19:370421 | A | C | 1 | a0001c0001t0001g0295 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.753+784T>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370421 | |||||||
| chr19:370434 | C | A | 1 | a0001c0001t0001g0236 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.753+771G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370434 | |||||||
| chr19:370465 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.753+740G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370465 | |||||||
| chr19:370469 | G | A | 43 | a0001c0001t0001g0017 a0001c0001t0001g0167 a0001c0001t0001g0177 others(40): Show |
46 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.753+736C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370469 | |||||||
| chr19:370497 | A | G | 2 | a0002c0002t0001g0248 a0002c0002t0001g0323 |
2 | HG00673.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.753+708T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370497 | |||||||
| chr19:370508 | A | AT | 203 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0019 others(200): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.753+696dupA | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370508 | |||||||
| chr19:370508 | A | ATT | 16 | a0001c0001t0001g0150 a0001c0001t0001g0210 a0001c0001t0001g0211 others(13): Show |
18 | HG00423.hp2 HG00735.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.753+695_753+696dup others(2): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370508 | |||||||
| chr19:370508 | AT | A | 43 | a0001c0001t0001g0148 a0001c0001t0001g0151 a0001c0001t0001g0170 others(40): Show |
48 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.753+696delA | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370508 | |||||||
| chr19:370552 | A | G | 2 | a0001c0001t0006g0230 a0001c0001t0026g0122 |
2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.753+653T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370552 | |||||||
| chr19:370572 | G | T | 16 | a0001c0001t0001g0189 a0001c0001t0001g0209 a0001c0001t0001g0295 others(13): Show |
16 | HG00099.hp2 HG00438.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.753+633C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370572 | |||||||
| chr19:370591 | C | A | 52 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0150 others(49): Show |
61 | HG00423.hp2 HG00735.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.753+614G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370591 | |||||||
| chr19:370593 | A | G | 43 | a0001c0001t0001g0017 a0001c0001t0001g0167 a0001c0001t0001g0177 others(40): Show |
46 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.753+612T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370593 | |||||||
| chr19:370602 | A | G | 311 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0019 others(308): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.753+603T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370602 | |||||||
| chr19:370690 | C | T | 2 | a0002c0002t0002g0077 a0002c0002t0003g0185 |
2 | NA18947.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.753+515G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370690 | |||||||
| chr19:370742 | C | T | 1 | a0003c0003t0002g0097 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.753+463G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370742 | |||||||
| chr19:370747 | G | A | 6 | a0001c0001t0001g0258 a0001c0001t0001g0285 a0001c0001t0002g0096 others(3): Show |
6 | HG00558.hp2 HG00597.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.753+458C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370747 | |||||||
| chr19:370802 | G | A | 25 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(22): Show |
26 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.753+403C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370802 | |||||||
| chr19:370802 | G | T | 1 | a0003c0010t0044g0138 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.753+403C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370802 | |||||||
| chr19:370803 | C | T | 69 | a0001c0001t0001g0017 a0001c0001t0001g0152 a0001c0001t0001g0153 others(66): Show |
73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.753+402G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370803 | |||||||
| chr19:370825 | G | C | 2 | a0001c0004t0007g0040 a0001c0023t0030g0126 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.753+380C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370825 | |||||||
| chr19:370866 | AG | A | 210 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0019 others(207): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.753+338delC | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370866 | |||||||
| chr19:370896 | T | G | 25 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(22): Show |
26 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.753+309A>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370896 | |||||||
| chr19:370935 | G | A | 1 | a0001c0001t0025g0117 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.753+270C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 370935 | |||||||
| chr19:371001 | C | A | 25 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(22): Show |
26 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.753+204G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 371001 | |||||||
| chr19:371129 | G | A | 6 | a0004c0005t0010g0011 a0004c0005t0011g0037 a0004c0005t0018g0041 others(3): Show |
7 | HG02818.hp1 HG02886.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+76C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 371129 | |||||||
| chr19:371176 | G | T | 1 | a0001c0004t0003g0134 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.753+29C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 371176 | |||||||
| chr19:371183 | G | A | 2 | a0001c0001t0004g0005 a0001c0001t0007g0057 |
3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.753+22C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 371183 | |||||||
| chr19:371194 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.753+11C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 6/7 | chr19 | 371194 | |||||||
| chr19:371355 | C | T | 9 | a0001c0006t0001g0321 a0001c0006t0002g0065 a0001c0006t0002g0083 others(6): Show |
9 | HG00438.hp1 HG02056.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.636-33G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371355 | |||||||
| chr19:371365 | TGG | T | 10 | a0001c0001t0001g0172 a0001c0004t0007g0040 a0001c0023t0030g0126 others(7): Show |
11 | HG02818.hp1 HG02886.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.636-45_636-44delCC | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371365 | |||||||
| chr19:371367 | G | T | 9 | a0001c0006t0001g0321 a0001c0006t0002g0065 a0001c0006t0002g0083 others(6): Show |
9 | HG00438.hp1 HG02056.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.636-45C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371367 | |||||||
| chr19:371369 | G | T | 59 | a0001c0001t0001g0019 a0001c0001t0001g0182 a0001c0001t0001g0193 others(56): Show |
62 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.636-47C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371369 | |||||||
| chr19:371369 | GGT | G | 73 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0153 others(70): Show |
79 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.636-49_636-48delAC | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371369 | |||||||
| chr19:371371 | T | G | 2 | a0002c0002t0001g0178 a0002c0002t0001g0179 |
2 | NA18944.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.636-49A>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371371 | |||||||
| chr19:371396 | G | C | 284 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0019 others(281): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.636-74C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371396 | |||||||
| chr19:371396 | G | GTC | 12 | a0001c0001t0001g0026 a0001c0001t0001g0254 a0001c0001t0001g0261 others(9): Show |
13 | HG00544.hp2 HG01891.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.636-75_636-74insGA | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371396 | |||||||
| chr19:371396 | G | GTGTC | 4 | a0002c0002t0001g0173 a0002c0002t0001g0237 a0002c0002t0002g0066 others(1): Show |
4 | HG01167.hp1 HG02602.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.636-75_636-74insGA others(2): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371396 | |||||||
| chr19:371396 | G | GTGTGTGT others(3): Show |
7 | a0001c0006t0001g0321 a0001c0006t0002g0065 a0001c0006t0003g0322 others(4): Show |
7 | HG00438.hp1 HG01975.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.636-75_636-74insGA others(8): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371396 | |||||||
| chr19:371396 | G | GTGTGTGT others(5): Show |
4 | a0001c0001t0036g0149 a0001c0006t0002g0083 a0001c0017t0001g0141 others(1): Show |
4 | HG02258.hp2 NA18942.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.636-75_636-74insGA others(10): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371396 | |||||||
| chr19:371396 | G | GTGTGTGT others(7): Show |
1 | a0001c0006t0002g0108 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.636-75_636-74insGA others(12): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371396 | |||||||
| chr19:371537 | A | G | 2 | a0001c0001t0001g0184 a0001c0004t0002g0043 |
2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.636-215T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371537 | |||||||
| chr19:371560 | G | T | 2 | a0001c0004t0007g0040 a0001c0023t0030g0126 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.636-238C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371560 | |||||||
| chr19:371718 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.636-396C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371718 | |||||||
| chr19:371837 | A | C | 1 | a0001c0001t0001g0281 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.636-515T>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371837 | |||||||
| chr19:371868 | T | A | 1 | a0001c0001t0011g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.636-546A>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371868 | |||||||
| chr19:371899 | C | T | 84 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0153 others(81): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.636-577G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371899 | |||||||
| chr19:371967 | G | A | 44 | a0001c0001t0001g0017 a0001c0001t0001g0165 a0001c0001t0001g0167 others(41): Show |
47 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.636-645C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 371967 | |||||||
| chr19:372043 | G | A | 1 | a0002c0002t0037g0180 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.635+588C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 372043 | |||||||
| chr19:372052 | AGTGCACA others(3): Show |
A | 1 | a0002c0002t0001g0203 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.635+569_635+578del others(10): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 372052 | |||||||
| chr19:372084 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.635+547G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 372084 | |||||||
| chr19:372132 | A | G | 2 | a0001c0001t0001g0261 a0001c0013t0001g0144 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.635+499T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 372132 | |||||||
| chr19:372181 | GAT | G | 54 | a0001c0001t0001g0148 a0001c0001t0001g0170 a0001c0001t0001g0184 others(51): Show |
59 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.635+448_635+449del others(2): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 372181 | |||||||
| chr19:372348 | C | G | 47 | a0001c0001t0001g0017 a0001c0001t0001g0165 a0001c0001t0001g0167 others(44): Show |
50 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.635+283G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 372348 | |||||||
| chr19:372354 | G | C | 8 | a0001c0001t0004g0056 a0001c0001t0004g0104 a0001c0001t0006g0303 others(5): Show |
8 | HG01891.hp1 HG02486.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.635+277C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 372354 | |||||||
| chr19:372389 | C | T | 1 | a0001c0001t0006g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.635+242G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 372389 | |||||||
| chr19:372433 | CAAGCAGC others(21): Show |
C | 1 | a0003c0003t0001g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.635+170_635+197del others(28): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 372433 | |||||||
| chr19:372531 | G | C | 2 | a0001c0001t0001g0261 a0001c0013t0001g0144 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.635+100C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 372531 | |||||||
| chr19:372551 | A | G | 311 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0019 others(308): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.635+80T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 372551 | |||||||
| chr19:372602 | G | A | 2 | a0002c0002t0001g0202 a0002c0002t0001g0203 |
2 | NA18989.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.635+29C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 372602 | |||||||
| chr19:372612 | C | A | 1 | a0002c0002t0002g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.635+19G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 5/7 | chr19 | 372612 | |||||||
| chr19:372719 | G | A | 1 | a0001c0001t0011g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.566-19C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 372719 | |||||||
| chr19:372737 | T | C | 53 | a0001c0001t0001g0148 a0001c0001t0001g0170 a0001c0001t0001g0184 others(50): Show |
56 | HG00099.hp1 HG00735.hp1 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.566-37A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 372737 | |||||||
| chr19:372751 | A | T | 1 | a0002c0002t0001g0316 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.566-51T>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 372751 | |||||||
| chr19:372775 | G | A | 52 | a0001c0001t0001g0148 a0001c0001t0001g0170 a0001c0001t0001g0184 others(49): Show |
55 | HG00099.hp1 HG00735.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.566-75C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 372775 | |||||||
| chr19:372867 | T | C | 312 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0019 others(309): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.566-167A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 372867 | |||||||
| chr19:372875 | C | T | 50 | a0001c0001t0001g0017 a0001c0001t0001g0158 a0001c0001t0001g0165 others(47): Show |
53 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.566-175G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 372875 | |||||||
| chr19:372936 | G | A | 1 | a0004c0005t0002g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.566-236C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 372936 | |||||||
| chr19:372966 | G | A | 2 | a0001c0001t0004g0005 a0001c0001t0007g0057 |
3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.566-266C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 372966 | |||||||
| chr19:373018 | A | G | 2 | a0001c0001t0004g0005 a0001c0001t0007g0057 |
3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.566-318T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 373018 | |||||||
| chr19:373026 | T | G | 22 | a0001c0001t0001g0166 a0001c0001t0001g0181 a0001c0001t0002g0099 others(19): Show |
23 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.566-326A>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 373026 | |||||||
| chr19:373051 | G | T | 1 | a0002c0002t0001g0198 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.566-351C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 373051 | |||||||
| chr19:373077 | T | C | 1 | a0001c0001t0003g0302 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.566-377A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 373077 | |||||||
| chr19:373115 | C | G | 1 | a0001c0004t0003g0135 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.565+355G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 373115 | |||||||
| chr19:373418 | T | C | 1 | a0001c0023t0030g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.565+52A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 373418 | |||||||
| chr19:373425 | C | T | 2 | a0001c0001t0010g0273 a0001c0004t0002g0039 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.565+45G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 373425 | |||||||
| chr19:373431 | C | G | 1 | a0002c0002t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.565+39G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 373431 | |||||||
| chr19:373433 | G | C | 1 | a0002c0002t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.565+37C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 373433 | |||||||
| chr19:373456 | C | T | 1 | a0001c0004t0003g0135 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.565+14G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 4/7 | chr19 | 373456 | |||||||
| chr19:373618 | GC | G | 113 | a0001c0001t0001g0013 a0001c0001t0001g0148 a0001c0001t0001g0150 others(110): Show |
128 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.504-88delG | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 3/7 | chr19 | 373618 | |||||||
| chr19:373619 | C | G | 1 | a0002c0002t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.504-88G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 3/7 | chr19 | 373619 | |||||||
| chr19:373673 | G | A | 56 | a0001c0001t0001g0017 a0001c0001t0001g0152 a0001c0001t0001g0153 others(53): Show |
60 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.504-142C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 3/7 | chr19 | 373673 | |||||||
| chr19:373677 | G | A | 7 | a0001c0001t0003g0213 a0001c0001t0003g0214 a0001c0001t0005g0076 others(4): Show |
7 | HG00741.hp2 HG01099.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.504-146C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 3/7 | chr19 | 373677 | |||||||
| chr19:373684 | G | A | 1 | a0002c0002t0001g0307 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.504-153C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 3/7 | chr19 | 373684 | |||||||
| chr19:373689 | G | A | 1 | a0001c0004t0001g0133 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.504-158C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 3/7 | chr19 | 373689 | |||||||
| chr19:373690 | C | T | 24 | a0001c0001t0001g0017 a0001c0001t0001g0148 a0001c0001t0001g0158 others(21): Show |
26 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.504-159G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 3/7 | chr19 | 373690 | |||||||
| chr19:373775 | TCCTGGGA others(20): Show |
T | 1 | a0003c0003t0001g0331 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.503+138_503+164del others(27): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 3/7 | chr19 | 373775 | |||||||
| chr19:373788 | C | A | 1 | a0002c0002t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.503+152G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 3/7 | chr19 | 373788 | |||||||
| chr19:373897 | G | C | 46 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0001g0209 others(43): Show |
49 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.503+43C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 3/7 | chr19 | 373897 | |||||||
| chr19:373916 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0003g0197 |
2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.503+24G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 3/7 | chr19 | 373916 | |||||||
| chr19:374016 | G | A | 31 | a0001c0001t0001g0017 a0001c0001t0001g0158 a0001c0001t0001g0165 others(28): Show |
34 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(31): Show |
splice_region_variant&intron_variant | LOW | c.432-5C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 2/7 | chr19 | 374016 | |||||||
| chr19:374149 | A | C | 2 | a0001c0023t0030g0126 a0005c0009t0008g0124 |
2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.432-138T>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 2/7 | chr19 | 374149 | |||||||
| chr19:374151 | C | A | 18 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0050 others(15): Show |
18 | HG02074.hp2 HG02129.hp2 HG04204.hp1 others(15): Show |
intron_variant | MODIFIER | c.432-140G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 2/7 | chr19 | 374151 | |||||||
| chr19:374210 | C | T | 1 | a0003c0003t0001g0229 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.431+89G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 2/7 | chr19 | 374210 | |||||||
| chr19:374236 | G | A | 1 | a0002c0002t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.431+63C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 2/7 | chr19 | 374236 | |||||||
| chr19:374240 | G | A | 5 | a0001c0001t0006g0169 a0001c0001t0024g0116 a0001c0001t0025g0117 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.431+59C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 2/7 | chr19 | 374240 | |||||||
| chr19:374253 | G | A | 1 | a0002c0002t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.431+46C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 2/7 | chr19 | 374253 | |||||||
| chr19:374264 | T | A | 1 | a0002c0002t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.431+35A>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 2/7 | chr19 | 374264 | |||||||
| chr19:374265 | G | GAAGCCGC others(6): Show |
1 | a0002c0002t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.431+33_431+34insAG others(11): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 2/7 | chr19 | 374265 | |||||||
| chr19:374266 | C | G | 1 | a0002c0002t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.431+33G>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 2/7 | chr19 | 374266 | |||||||
| chr19:374279 | G | A | 1 | a0001c0001t0004g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.431+20C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 2/7 | chr19 | 374279 | |||||||
| chr19:374291 | G | A | 1 | a0001c0023t0030g0126 | 1 | HG03453.hp1 | splice_region_variant&intron_variant | LOW | c.431+8C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 2/7 | chr19 | 374291 | |||||||
| chr19:374439 | G | A | 1 | a0001c0001t0042g0296 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.309-18C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 374439 | |||||||
| chr19:374453 | T | C | 155 | a0001c0001t0001g0013 a0001c0001t0001g0148 a0001c0001t0001g0166 others(152): Show |
171 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.309-32A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 374453 | |||||||
| chr19:374467 | G | A | 3 | a0001c0001t0001g0232 a0001c0001t0002g0094 a0001c0001t0002g0098 |
3 | HG00280.hp1 HG00280.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.309-46C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 374467 | |||||||
| chr19:374492 | G | C | 200 | a0001c0001t0001g0017 a0001c0001t0001g0158 a0001c0001t0001g0172 others(197): Show |
222 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.309-71C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 374492 | |||||||
| chr19:374493 | T | C | 1 | a0001c0001t0010g0273 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.309-72A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 374493 | |||||||
| chr19:374547 | T | C | 101 | a0001c0001t0001g0017 a0001c0001t0001g0188 a0001c0001t0001g0189 others(98): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.309-126A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 374547 | |||||||
| chr19:374589 | A | AGGCCTGG others(30): Show |
1 | a0001c0001t0005g0053 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.309-205_309-169dup others(37): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 374589 | |||||||
| chr19:374604 | G | A | 18 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0210 others(15): Show |
19 | HG00099.hp2 HG00609.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.309-183C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 374604 | |||||||
| chr19:374636 | T | C | 7 | a0001c0001t0001g0215 a0001c0001t0002g0081 a0001c0001t0003g0213 others(4): Show |
8 | HG00735.hp2 HG00741.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.309-215A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 374636 | |||||||
| chr19:374704 | C | T | 68 | a0001c0001t0001g0019 a0001c0001t0001g0150 a0001c0001t0001g0151 others(65): Show |
75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.309-283G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 374704 | |||||||
| chr19:374872 | G | GAAGATGC others(20): Show |
1 | a0008c0027t0001g0216 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.309-478_309-452dup others(27): Show |
THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 374872 | |||||||
| chr19:374886 | C | T | 1 | a0002c0002t0003g0304 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.309-465G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 374886 | |||||||
| chr19:374925 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.309-504C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 374925 | |||||||
| chr19:374996 | G | T | 1 | a0002c0002t0001g0217 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.309-575C>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 374996 | |||||||
| chr19:375008 | A | T | 7 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0050 others(4): Show |
7 | HG02074.hp2 HG02129.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.309-587T>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375008 | |||||||
| chr19:375010 | T | C | 4 | a0001c0001t0033g0299 a0001c0001t0042g0296 a0004c0008t0001g0298 others(1): Show |
4 | HG02895.hp2 HG03540.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.309-589A>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375010 | |||||||
| chr19:375035 | T | A | 1 | a0001c0001t0001g0300 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.309-614A>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375035 | |||||||
| chr19:375039 | C | T | 92 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0150 others(89): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.309-618G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375039 | |||||||
| chr19:375220 | G | A | 17 | a0001c0001t0001g0301 a0001c0001t0002g0004 a0001c0001t0002g0045 others(14): Show |
23 | HG01109.hp1 HG01168.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.308+443C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375220 | |||||||
| chr19:375272 | G | C | 3 | a0001c0001t0001g0335 a0001c0001t0002g0115 a0004c0008t0004g0114 |
3 | HG02280.hp1 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.308+391C>G | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375272 | |||||||
| chr19:375295 | CT | C | 35 | a0001c0001t0001g0026 a0001c0001t0001g0335 a0001c0001t0002g0004 others(32): Show |
41 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.308+367delA | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375295 | |||||||
| chr19:375296 | T | A | 3 | a0001c0001t0004g0104 a0005c0009t0008g0124 a0005c0009t0029g0125 |
3 | HG02055.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.308+367A>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375296 | |||||||
| chr19:375327 | T | G | 37 | a0001c0001t0001g0026 a0001c0001t0001g0335 a0001c0001t0002g0100 others(34): Show |
39 | HG00741.hp1 HG01192.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.308+336A>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375327 | |||||||
| chr19:375345 | C | A | 1 | a0001c0001t0004g0104 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.308+318G>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375345 | |||||||
| chr19:375366 | C | T | 17 | a0001c0001t0002g0004 a0001c0001t0002g0045 a0001c0001t0002g0046 others(14): Show |
22 | HG02074.hp2 HG02129.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.308+297G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375366 | |||||||
| chr19:375368 | C | T | 2 | a0001c0001t0019g0047 a0004c0020t0002g0048 |
2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.308+295G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375368 | |||||||
| chr19:375470 | G | A | 1 | a0001c0004t0016g0044 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.308+193C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375470 | |||||||
| chr19:375487 | C | T | 2 | a0001c0001t0002g0045 a0001c0001t0002g0046 |
2 | NA19000.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.308+176G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375487 | |||||||
| chr19:375493 | A | G | 290 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0019 others(287): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.308+170T>C | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375493 | |||||||
| chr19:375551 | G | A | 3 | a0001c0001t0001g0335 a0001c0001t0002g0115 a0004c0008t0004g0114 |
3 | HG02280.hp1 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.308+112C>T | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375551 | |||||||
| chr19:375557 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.308+106G>A | THEG | ENSG00000105549.11 | transcript | ENST00000342640.9 | protein_coding | 1/7 | chr19 | 375557 |