Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11262 |
| ensemblid | ENSG00000079263.19 |
| hgncid | 17133 |
| symbol | SP140 |
| name | SP140 nuclear body protein |
| refseq_nuc | NM_007237.5 |
| refseq_prot | NP_009168.4 |
| ensembl_nuc | ENST00000392045.8 |
| ensembl_prot | ENSP00000375899.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 230225736 |
| end | 230313215 |
| strand | + |
| ver | v1.2 |
| region | chr2:230225736-230313215 |
| region5000 | chr2:230220736-230318215 |
| regionname0 | SP140_chr2_230225736_230313215 |
| regionname5000 | SP140_chr2_230220736_230318215 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 867 | 269 | 61 | 42 | 124 | 5 | 36 | 101 | SP140_chr2_230220736_230318215 | SP140 | MAQQG others(862): Show |
chr2 | 230220736 | 230318215 |
| a0002 | 0/0 | 867 | 35 | 2 | 9 | 18 | 3 | 3 | 14 | SP140_chr2_230220736_230318215 | SP140 | MAQQG others(862): Show |
chr2 | 230220736 | 230318215 |
| a0003 | 0/0 | 867 | 25 | 2 | 15 | 0 | 5 | 3 | 0 | SP140_chr2_230220736_230318215 | SP140 | MAQQG others(862): Show |
chr2 | 230220736 | 230318215 |
| a0004 | 0/0 | 867 | 16 | 14 | 0 | 1 | 0 | 1 | 1 | SP140_chr2_230220736_230318215 | SP140 | MAQQG others(862): Show |
chr2 | 230220736 | 230318215 |
| a0005 | 1/0 | 867 | 9 | 0 | 2 | 1 | 4 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | MAQQG others(862): Show |
chr2 | 230220736 | 230318215 |
| a0006 | 0/0 | 867 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | MAQQG others(862): Show |
chr2 | 230220736 | 230318215 |
| a0007 | 0/0 | 867 | 3 | 2 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | MAQQG others(862): Show |
chr2 | 230220736 | 230318215 |
| a0008 | 0/0 | 867 | 3 | 0 | 1 | 2 | 0 | 0 | 2 | SP140_chr2_230220736_230318215 | SP140 | MAQQG others(862): Show |
chr2 | 230220736 | 230318215 |
| a0009 | 0/0 | 867 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | MAQQG others(862): Show |
chr2 | 230220736 | 230318215 |
| a0010 | 0/0 | 867 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | MAQQG others(862): Show |
chr2 | 230220736 | 230318215 |
| a0011 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | MAQQG others(862): Show |
chr2 | 230220736 | 230318215 |
| a0012 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | MAQQG others(862): Show |
chr2 | 230220736 | 230318215 |
| a0013 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | MAQQG others(862): Show |
chr2 | 230220736 | 230318215 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2601 | 255 | 55 | 41 | 123 | 3 | 32 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0001c0006 | 0/0 | 2601 | 11 | 6 | 1 | 0 | 1 | 3 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0001c0011 | 0/0 | 2601 | 2 | 0 | 0 | 1 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0001c0016 | 0/0 | 2601 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0002c0002 | 0/0 | 2601 | 30 | 2 | 7 | 17 | 2 | 2 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0002c0008 | 0/0 | 2601 | 5 | 0 | 2 | 1 | 1 | 1 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0003c0004 | 0/0 | 2601 | 14 | 2 | 10 | 0 | 0 | 2 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0003c0005 | 0/0 | 2601 | 11 | 0 | 5 | 0 | 5 | 1 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0004c0003 | 0/0 | 2601 | 16 | 14 | 0 | 1 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0005c0007 | 1/0 | 2601 | 9 | 0 | 2 | 1 | 4 | 1 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0006c0009 | 0/0 | 2601 | 4 | 4 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0007c0012 | 0/0 | 2601 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0007c0017 | 0/0 | 2601 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0008c0010 | 0/0 | 2601 | 2 | 0 | 0 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0008c0019 | 0/0 | 2601 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0009c0013 | 0/0 | 2601 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0010c0020 | 0/0 | 2601 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0011c0014 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0012c0018 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 | ||
| a0013c0015 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | ATGGC others(2596): Show |
chr2 | 230220736 | 230318215 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3244 | 212 | 43 | 35 | 104 | 3 | 26 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0001c0001t0002 | 0/0 | 3244 | 37 | 10 | 5 | 17 | 0 | 5 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0001c0001t0004 | 0/0 | 3244 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0001c0001t0005 | 0/0 | 3244 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0001c0001t0006 | 0/0 | 3244 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0001c0001t0007 | 0/0 | 3244 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0001c0001t0009 | 0/0 | 3244 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0001c0006t0001 | 0/0 | 3244 | 7 | 2 | 1 | 0 | 1 | 3 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0001c0006t0002 | 0/0 | 3244 | 4 | 4 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0001c0011t0001 | 0/0 | 3244 | 2 | 0 | 0 | 1 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0001c0016t0001 | 0/0 | 3244 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0002c0002t0001 | 0/0 | 3244 | 30 | 2 | 7 | 17 | 2 | 2 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0002c0008t0001 | 0/0 | 3244 | 4 | 0 | 1 | 1 | 1 | 1 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0002c0008t0002 | 0/0 | 3244 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0003c0004t0003 | 0/0 | 3244 | 13 | 1 | 10 | 0 | 0 | 2 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0003c0004t0010 | 0/0 | 3244 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0003c0005t0003 | 0/0 | 3244 | 10 | 0 | 4 | 0 | 5 | 1 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0003c0005t0008 | 0/0 | 3244 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0004c0003t0001 | 0/0 | 3244 | 16 | 14 | 0 | 1 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0005c0007t0001 | 1/0 | 3244 | 9 | 0 | 2 | 1 | 4 | 1 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0006c0009t0002 | 0/0 | 3244 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0006c0009t0004 | 0/0 | 3244 | 3 | 3 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0007c0012t0001 | 0/0 | 3244 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0007c0017t0001 | 0/0 | 3244 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0008c0010t0001 | 0/0 | 3244 | 2 | 0 | 0 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0008c0019t0001 | 0/0 | 3244 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0009c0013t0001 | 0/0 | 3244 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0010c0020t0001 | 0/0 | 3244 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0011c0014t0001 | 0/0 | 3244 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0012c0018t0001 | 0/0 | 3244 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| a0013c0015t0001 | 0/0 | 3244 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | CTTTT others(3239): Show |
chr2 | 230220736 | 230318215 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0007g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0001t0009g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0006t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0006t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0006t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0006t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0006t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0006t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0006t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0006t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0006t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0011t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0011t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0001c0016t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0008t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0008t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0008t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0002c0008t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0004t0003g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0004t0003g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0004t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0004t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0004t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0004t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0004t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0004t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0004t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0004t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0004t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0004t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0005t0003g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0005t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0005t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0005t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0005t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0005t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0005t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0005t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0005t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0003c0005t0008g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0004c0003t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0005c0007t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0005c0007t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0005c0007t0001g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0005c0007t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0005c0007t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0005c0007t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0005c0007t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0005c0007t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0006c0009t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0006c0009t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0006c0009t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0006c0009t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0007c0012t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0007c0012t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0007c0017t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0008c0010t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0008c0010t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0008c0019t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0009c0013t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0009c0013t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0010c0020t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0011c0014t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0012c0018t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| a0013c0015t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | GBR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | GBR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00140 | hp1 | a0001 | c0006 | t0001 | g0035 | EUR | GBR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00140 | hp2 | a0003 | c0005 | t0003 | g0105 | EUR | GBR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00280 | hp1 | a0005 | c0007 | t0001 | g0100 | EUR | FIN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | FIN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00323 | hp1 | a0003 | c0005 | t0003 | g0166 | EUR | FIN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00323 | hp2 | a0007 | c0017 | t0001 | g0061 | EUR | FIN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00408 | hp1 | a0005 | c0007 | t0001 | g0066 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0316 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0332 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00597 | hp2 | a0001 | c0001 | t0009 | g0072 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00642 | hp2 | a0002 | c0008 | t0002 | g0336 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00738 | hp2 | a0003 | c0004 | t0003 | g0031 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01069 | hp1 | a0003 | c0005 | t0003 | g0188 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01070 | hp1 | a0005 | c0007 | t0001 | g0010 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0326 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01071 | hp1 | a0005 | c0007 | t0001 | g0010 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01071 | hp2 | a0003 | c0005 | t0003 | g0187 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01169 | hp1 | a0003 | c0004 | t0003 | g0008 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01175 | hp1 | a0003 | c0005 | t0003 | g0218 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01243 | hp1 | a0003 | c0004 | t0003 | g0038 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0126 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01255 | hp1 | a0003 | c0005 | t0003 | g0110 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01256 | hp1 | a0003 | c0004 | t0003 | g0028 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01256 | hp2 | a0003 | c0004 | t0003 | g0006 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01258 | hp1 | a0003 | c0004 | t0003 | g0006 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01261 | hp1 | a0010 | c0020 | t0001 | g0137 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0313 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01346 | hp2 | a0003 | c0004 | t0003 | g0040 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0330 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01358 | hp2 | a0001 | c0006 | t0001 | g0039 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01361 | hp1 | a0002 | c0008 | t0001 | g0022 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01433 | hp2 | a0003 | c0004 | t0003 | g0041 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01496 | hp1 | a0003 | c0004 | t0003 | g0032 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01515 | hp1 | a0005 | c0007 | t0001 | g0069 | EUR | IBS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0322 | EUR | IBS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0319 | EUR | IBS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01516 | hp2 | a0003 | c0005 | t0003 | g0013 | EUR | IBS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01517 | hp1 | a0005 | c0007 | t0001 | g0097 | EUR | IBS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01517 | hp2 | a0003 | c0005 | t0003 | g0013 | EUR | IBS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01884 | hp1 | a0004 | c0003 | t0001 | g0262 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01884 | hp2 | a0004 | c0003 | t0001 | g0311 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0338 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0153 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0329 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01978 | hp1 | a0003 | c0005 | t0008 | g0217 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0320 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0328 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02145 | hp1 | a0009 | c0013 | t0001 | g0143 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02145 | hp2 | a0004 | c0003 | t0001 | g0053 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0323 | EAS | CDX | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02257 | hp1 | a0009 | c0013 | t0001 | g0144 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02257 | hp2 | a0006 | c0009 | t0004 | g0159 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02258 | hp1 | a0003 | c0004 | t0003 | g0030 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02280 | hp1 | a0004 | c0003 | t0001 | g0300 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02300 | hp2 | a0008 | c0019 | t0001 | g0034 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0318 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02451 | hp2 | a0007 | c0012 | t0001 | g0024 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0312 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02602 | hp1 | a0001 | c0006 | t0001 | g0037 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0184 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02615 | hp1 | a0004 | c0003 | t0001 | g0302 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02622 | hp2 | a0004 | c0003 | t0001 | g0261 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02717 | hp1 | a0004 | c0003 | t0001 | g0304 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02735 | hp1 | a0001 | c0006 | t0001 | g0036 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02738 | hp1 | a0005 | c0007 | t0001 | g0127 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02738 | hp2 | a0003 | c0004 | t0003 | g0043 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02809 | hp1 | a0004 | c0003 | t0001 | g0303 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02809 | hp2 | a0006 | c0009 | t0004 | g0160 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02818 | hp2 | a0001 | c0006 | t0001 | g0047 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02886 | hp1 | a0004 | c0003 | t0001 | g0263 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02896 | hp2 | a0001 | c0006 | t0001 | g0046 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02970 | hp2 | a0007 | c0012 | t0001 | g0025 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03041 | hp1 | a0004 | c0003 | t0001 | g0305 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03195 | hp2 | a0004 | c0003 | t0001 | g0264 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03209 | hp2 | a0012 | c0018 | t0001 | g0249 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03225 | hp1 | a0004 | c0003 | t0001 | g0267 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03225 | hp2 | a0004 | c0003 | t0001 | g0301 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03239 | hp2 | a0003 | c0004 | t0003 | g0008 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03453 | hp2 | a0001 | c0006 | t0002 | g0007 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03486 | hp1 | a0013 | c0015 | t0001 | g0308 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03491 | hp1 | a0001 | c0006 | t0001 | g0045 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03516 | hp1 | a0001 | c0006 | t0002 | g0044 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0151 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03831 | hp1 | a0003 | c0005 | t0003 | g0203 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03834 | hp2 | a0001 | c0016 | t0001 | g0275 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03927 | hp1 | a0004 | c0003 | t0001 | g0340 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0339 | SAS | STU | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18522 | hp1 | a0006 | c0009 | t0002 | g0157 | AFR | YRI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | YRI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | YRI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0250 | AFR | YRI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18939 | hp1 | a0008 | c0010 | t0001 | g0117 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18944 | hp1 | a0001 | c0011 | t0001 | g0202 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0093 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18954 | hp2 | a0002 | c0008 | t0001 | g0321 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0333 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19002 | hp2 | a0004 | c0003 | t0001 | g0337 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | LWK | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | LWK | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0331 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19079 | hp1 | a0008 | c0010 | t0001 | g0074 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | YRI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA19240 | hp2 | a0004 | c0003 | t0001 | g0229 | AFR | YRI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ASW | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ASW | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA20752 | hp1 | a0001 | c0011 | t0001 | g0169 | EUR | TSI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA20752 | hp2 | a0005 | c0007 | t0001 | g0099 | EUR | TSI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA20805 | hp1 | a0002 | c0008 | t0001 | g0022 | EUR | TSI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA20805 | hp2 | a0003 | c0005 | t0003 | g0104 | EUR | TSI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | GIH | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA20905 | hp2 | a0002 | c0008 | t0001 | g0317 | SAS | GIH | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01123 | hp1 | a0003 | c0004 | t0003 | g0042 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02486 | hp1 | a0011 | c0014 | t0001 | g0259 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02559 | hp1 | a0006 | c0009 | t0004 | g0158 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | USA | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| HG06807 | hp2 | a0003 | c0004 | t0010 | g0033 | AFR | USA | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | USA | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA20300 | hp2 | a0001 | c0006 | t0002 | g0007 | AFR | USA | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| NA21309 | hp2 | a0001 | c0006 | t0002 | g0029 | AFR | LWK | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0215 | REF | REF | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| homoSapiens | grch38p0 | a0005 | c0007 | t0001 | g0067 | REF | REF | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:230245054 | C | T | 1 | a0010 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.638C>T | p.Ala213Val | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/27 | 747/3244 | 638/2604 | 213/867 | chr2 | 230245054 | |||
| chr2:230245934 | A | G | 1 | a0012 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.736A>G | p.Thr246Ala | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/27 | 845/3244 | 736/2604 | 246/867 | chr2 | 230245934 | |||
| chr2:230248903 | C | T | 1 | a0009 | 2 | HG02145.hp1 HG02257.hp1 |
missense_variant | MODERATE | c.911C>T | p.Thr304Ile | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/27 | 1020/3244 | 911/2604 | 304/867 | chr2 | 230248903 | |||
| chr2:230253326 | A | C | 4 | a0002 a0004 a0007 others(1): Show |
56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
missense_variant | MODERATE | c.1068A>C | p.Leu356Phe | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/27 | 1177/3244 | 1068/2604 | 356/867 | chr2 | 230253326 | |||
| chr2:230253394 | G | A | 1 | a0011 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1136G>A | p.Ser379Asn | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/27 | 1245/3244 | 1136/2604 | 379/867 | chr2 | 230253394 | |||
| chr2:230253406 | G | T | 1 | a0011 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1148G>T | p.Gly383Val | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/27 | 1257/3244 | 1148/2604 | 383/867 | chr2 | 230253406 | |||
| chr2:230255494 | G | C | 1 | a0007 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.1202G>C | p.Arg401Pro | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/27 | 1311/3244 | 1202/2604 | 401/867 | chr2 | 230255494 | |||
| chr2:230255526 | G | C | 1 | a0013 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1234G>C | p.Gly412Arg | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/27 | 1343/3244 | 1234/2604 | 412/867 | chr2 | 230255526 | |||
| chr2:230284382 | T | C | 2 | a0002 a0008 |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
missense_variant | MODERATE | c.1535T>C | p.Met512Thr | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/27 | 1644/3244 | 1535/2604 | 512/867 | chr2 | 230284382 | |||
| chr2:230284393 | G | A | 12 | a0001 a0002 a0003 others(9): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
missense_variant | MODERATE | c.1546G>A | p.Glu516Lys | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/27 | 1655/3244 | 1546/2604 | 516/867 | chr2 | 230284393 | |||
| chr2:230287918 | C | T | 1 | a0006 | 4 | HG02257.hp2 HG02559.hp1 HG02809.hp2 others(1): Show |
missense_variant | MODERATE | c.1672C>T | p.Arg558Cys | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/27 | 1781/3244 | 1672/2604 | 558/867 | chr2 | 230287918 | |||
| chr2:230310834 | T | C | 1 | a0003 | 25 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(22): Show |
missense_variant | MODERATE | c.2266T>C | p.Cys756Arg | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/27 | 2375/3244 | 2266/2604 | 756/867 | chr2 | 230310834 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:230245867 | C | T | 3 | a0001c0006 a0003c0004 a0008c0019 |
26 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(23): Show |
synonymous_variant | LOW | c.669C>T | p.Ser223Ser | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/27 | 778/3244 | 669/2604 | 223/867 | chr2 | 230245867 | |||
| chr2:230285801 | C | T | 1 | a0001c0016 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.1614C>T | p.Asn538Asn | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/27 | 1723/3244 | 1614/2604 | 538/867 | chr2 | 230285801 | |||
| chr2:230311481 | G | A | 5 | a0001c0011 a0002c0002 a0007c0017 others(2): Show |
36 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(33): Show |
synonymous_variant | LOW | c.2391G>A | p.Glu797Glu | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 26/27 | 2500/3244 | 2391/2604 | 797/867 | chr2 | 230311481 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:230225817 | G | T | 1 | a0003c0004t0010 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-28G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/27 | 28 | chr2 | 230225817 | ||||||
| chr2:230312900 | G | A | 1 | a0001c0001t0005 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*216G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 216 | chr2 | 230312900 | ||||||
| chr2:230312918 | A | T | 1 | a0001c0001t0009 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*234A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 234 | chr2 | 230312918 | ||||||
| chr2:230312974 | C | G | 1 | a0003c0005t0008 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 290 | chr2 | 230312974 | ||||||
| chr2:230313045 | T | C | 1 | a0001c0001t0006 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*361T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 361 | chr2 | 230313045 | ||||||
| chr2:230313107 | G | A | 4 | a0001c0001t0002 a0001c0006t0002 a0002c0008t0002 others(1): Show |
43 | HG00423.hp1 HG00642.hp1 HG00642.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*423G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 423 | chr2 | 230313107 | ||||||
| chr2:230313188 | A | G | 1 | a0001c0001t0007 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*504A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 504 | chr2 | 230313188 | ||||||
| chr2:230313189 | T | C | 4 | a0003c0004t0003 a0003c0004t0010 a0003c0005t0003 others(1): Show |
25 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*505T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 505 | chr2 | 230313189 | ||||||
| chr2:230313191 | T | C | 2 | a0001c0001t0004 a0006c0009t0004 |
5 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*507T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 507 | chr2 | 230313191 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:230225956 | T | G | 2 | a0007c0012t0001g0024 a0007c0012t0001g0025 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.59+53T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230225956 | |||||||
| chr2:230226309 | G | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 |
4 | HG01106.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+406G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230226309 | |||||||
| chr2:230226362 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.59+459A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230226362 | |||||||
| chr2:230226508 | T | G | 23 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(20): Show |
26 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.59+605T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230226508 | |||||||
| chr2:230226625 | C | G | 21 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(18): Show |
24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.59+722C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230226625 | |||||||
| chr2:230226626 | A | G | 21 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(18): Show |
24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.59+723A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230226626 | |||||||
| chr2:230226762 | C | CAAAAAAA others(4): Show |
3 | a0001c0006t0001g0045 a0001c0006t0001g0046 a0001c0006t0001g0047 |
3 | HG02818.hp2 HG02896.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.59+868_59+878dupAA others(9): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230226762 | ||||||
| chr2:230226762 | C | CAAAAAAA others(5): Show |
17 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(14): Show |
20 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.59+867_59+878dupAA others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230226762 | ||||||
| chr2:230226762 | C | CAAAAAAA others(6): Show |
1 | a0003c0004t0003g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.59+866_59+878dupAA others(11): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230226762 | ||||||
| chr2:230226762 | CA | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(206): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.59+878delA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230226762 | ||||||
| chr2:230226941 | G | A | 21 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(18): Show |
24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.59+1038G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230226941 | |||||||
| chr2:230226987 | T | C | 1 | a0002c0002t0001g0153 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.59+1084T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230226987 | |||||||
| chr2:230227037 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.59+1134C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230227037 | |||||||
| chr2:230227374 | A | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 |
4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+1471A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230227374 | |||||||
| chr2:230227451 | A | T | 33 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(30): Show |
37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.59+1548A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230227451 | |||||||
| chr2:230227491 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.59+1588T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230227491 | |||||||
| chr2:230227792 | C | T | 1 | a0001c0001t0004g0312 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.59+1889C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230227792 | |||||||
| chr2:230227818 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.59+1915G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230227818 | |||||||
| chr2:230228212 | T | C | 1 | a0011c0014t0001g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.59+2309T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228212 | |||||||
| chr2:230228238 | T | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 |
4 | HG01106.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+2335T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228238 | |||||||
| chr2:230228287 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.59+2384G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228287 | |||||||
| chr2:230228358 | C | T | 33 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(30): Show |
37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.59+2455C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228358 | |||||||
| chr2:230228453 | C | G | 37 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(34): Show |
43 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.59+2550C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228453 | |||||||
| chr2:230228770 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 |
4 | HG01106.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+2867A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228770 | |||||||
| chr2:230228819 | G | A | 1 | a0001c0006t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.59+2916G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228819 | |||||||
| chr2:230228866 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.59+2963T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228866 | |||||||
| chr2:230228914 | T | C | 6 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0230 others(3): Show |
9 | HG00423.hp1 NA18943.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.59+3011T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228914 | |||||||
| chr2:230229169 | T | C | 1 | a0001c0001t0001g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.59+3266T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230229169 | |||||||
| chr2:230229412 | T | C | 1 | a0003c0004t0003g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.59+3509T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230229412 | |||||||
| chr2:230229421 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.59+3518G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230229421 | |||||||
| chr2:230229456 | C | CT | 46 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(43): Show |
47 | HG00642.hp2 HG00673.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.59+3582dupT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | ||||||
| chr2:230229456 | C | CTT | 9 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(6): Show |
9 | HG01884.hp2 HG01981.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.59+3581_59+3582dup others(2): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | ||||||
| chr2:230229456 | CT | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(76): Show |
85 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.59+3582delT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | ||||||
| chr2:230229456 | CTT | C | 9 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(6): Show |
9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+3581_59+3582del others(2): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | ||||||
| chr2:230229456 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0027 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.59+3572_59+3582del others(11): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | ||||||
| chr2:230229456 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0026 |
3 | HG02615.hp2 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.59+3571_59+3582del others(12): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | ||||||
| chr2:230229456 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 |
4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+3570_59+3582del others(13): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | ||||||
| chr2:230229456 | CTTTTTTT others(7): Show |
C | 5 | a0004c0003t0001g0053 a0004c0003t0001g0261 a0004c0003t0001g0262 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.59+3569_59+3582del others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | ||||||
| chr2:230229536 | C | T | 1 | a0004c0003t0001g0340 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.59+3633C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230229536 | |||||||
| chr2:230229994 | G | T | 1 | a0001c0001t0001g0342 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.59+4091G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230229994 | |||||||
| chr2:230230384 | A | G | 1 | a0001c0001t0001g0299 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.59+4481A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230230384 | |||||||
| chr2:230230451 | C | T | 33 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(30): Show |
37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.59+4548C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230230451 | |||||||
| chr2:230230872 | T | C | 4 | a0001c0001t0005g0126 a0007c0012t0001g0024 a0007c0012t0001g0025 others(1): Show |
4 | HG00323.hp2 HG01243.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+4969T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230230872 | |||||||
| chr2:230230963 | T | C | 23 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(20): Show |
26 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.59+5060T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230230963 | |||||||
| chr2:230230993 | A | G | 6 | a0001c0001t0001g0020 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
7 | HG01109.hp2 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.59+5090A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230230993 | |||||||
| chr2:230231061 | T | A | 5 | a0004c0003t0001g0053 a0004c0003t0001g0261 a0004c0003t0001g0262 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.59+5158T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231061 | |||||||
| chr2:230231237 | A | G | 30 | a0001c0001t0001g0019 a0001c0001t0001g0260 a0001c0001t0001g0266 others(27): Show |
31 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.59+5334A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231237 | |||||||
| chr2:230231472 | C | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0228 a0004c0003t0001g0305 |
3 | HG01361.hp2 HG03041.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.59+5569C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231472 | |||||||
| chr2:230231547 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 |
4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-5536T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231547 | |||||||
| chr2:230231556 | C | T | 4 | a0001c0001t0005g0126 a0007c0012t0001g0024 a0007c0012t0001g0025 others(1): Show |
4 | HG00323.hp2 HG01243.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-5527C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231556 | |||||||
| chr2:230231561 | A | C | 1 | a0001c0001t0001g0213 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.60-5522A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231561 | |||||||
| chr2:230231611 | AG | A | 33 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(30): Show |
37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.60-5467delG | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230231611 | ||||||
| chr2:230231629 | A | G | 33 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(30): Show |
37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.60-5454A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231629 | |||||||
| chr2:230231656 | A | T | 2 | a0003c0004t0003g0008 a0003c0004t0003g0040 |
3 | HG01169.hp1 HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.60-5427A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231656 | |||||||
| chr2:230231711 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.60-5372T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231711 | |||||||
| chr2:230231801 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.60-5282G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231801 | |||||||
| chr2:230231899 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.60-5184C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231899 | |||||||
| chr2:230231948 | ATCCACCC others(7): Show |
A | 1 | a0004c0003t0001g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.60-5132_60-5119del others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230231948 | ||||||
| chr2:230232414 | T | C | 37 | a0001c0001t0005g0126 a0001c0006t0001g0035 a0001c0006t0001g0036 others(34): Show |
40 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.60-4669T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230232414 | |||||||
| chr2:230232466 | GGTT | G | 4 | a0001c0001t0005g0126 a0007c0012t0001g0024 a0007c0012t0001g0025 others(1): Show |
4 | HG00323.hp2 HG01243.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-4602_60-4600del others(3): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230232466 | ||||||
| chr2:230232582 | A | G | 1 | a0002c0002t0001g0335 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.60-4501A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230232582 | |||||||
| chr2:230232658 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.60-4425A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230232658 | |||||||
| chr2:230232701 | T | G | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.60-4382T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230232701 | |||||||
| chr2:230232845 | G | C | 13 | a0001c0001t0005g0126 a0004c0003t0001g0300 a0004c0003t0001g0301 others(10): Show |
13 | HG00323.hp2 HG01243.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.60-4238G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230232845 | |||||||
| chr2:230232863 | A | G | 33 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(30): Show |
37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.60-4220A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230232863 | |||||||
| chr2:230233269 | G | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(200): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.60-3814G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233269 | |||||||
| chr2:230233325 | A | G | 43 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(40): Show |
46 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.60-3758A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233325 | |||||||
| chr2:230233356 | C | A | 23 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(20): Show |
26 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.60-3727C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233356 | |||||||
| chr2:230233495 | A | C | 9 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0302 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.60-3588A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233495 | |||||||
| chr2:230233670 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.60-3413G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233670 | |||||||
| chr2:230233696 | AAAT | A | 4 | a0001c0001t0005g0126 a0007c0012t0001g0024 a0007c0012t0001g0025 others(1): Show |
4 | HG00323.hp2 HG01243.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-3381_60-3379del others(3): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230233696 | ||||||
| chr2:230233745 | T | C | 2 | a0007c0012t0001g0024 a0007c0012t0001g0025 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.60-3338T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233745 | |||||||
| chr2:230233763 | C | T | 36 | a0001c0001t0005g0126 a0001c0006t0001g0035 a0001c0006t0001g0036 others(33): Show |
39 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.60-3320C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233763 | |||||||
| chr2:230233900 | A | T | 1 | a0001c0001t0001g0207 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.60-3183A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233900 | |||||||
| chr2:230233987 | G | A | 3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.60-3096G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233987 | |||||||
| chr2:230234197 | G | A | 9 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0302 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.60-2886G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230234197 | |||||||
| chr2:230234276 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.60-2807A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230234276 | |||||||
| chr2:230234427 | A | T | 1 | a0001c0001t0002g0257 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.60-2656A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230234427 | |||||||
| chr2:230234444 | A | G | 2 | a0001c0001t0002g0253 a0001c0001t0002g0258 |
2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.60-2639A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230234444 | |||||||
| chr2:230234455 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(123): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.60-2628C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230234455 | |||||||
| chr2:230234489 | C | T | 58 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(55): Show |
61 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.60-2594C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230234489 | |||||||
| chr2:230235324 | A | G | 340 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(337): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.60-1759A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230235324 | |||||||
| chr2:230235347 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(146): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.60-1736T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230235347 | |||||||
| chr2:230235367 | T | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(146): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.60-1716T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230235367 | |||||||
| chr2:230235425 | T | G | 3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.60-1658T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230235425 | |||||||
| chr2:230235860 | T | C | 1 | a0005c0007t0001g0066 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.60-1223T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230235860 | |||||||
| chr2:230235868 | G | GT | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0055 others(25): Show |
30 | HG01175.hp2 HG02056.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.60-1190dupT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230235868 | ||||||
| chr2:230235868 | GT | G | 49 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0068 others(46): Show |
50 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.60-1190delT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230235868 | ||||||
| chr2:230235868 | GTT | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(111): Show |
127 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.60-1191_60-1190del others(2): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230235868 | ||||||
| chr2:230235963 | G | A | 1 | a0002c0002t0001g0333 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.60-1120G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230235963 | |||||||
| chr2:230236035 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.60-1048C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236035 | |||||||
| chr2:230236118 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 |
4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-965G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236118 | |||||||
| chr2:230236126 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0268 |
2 | HG01169.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.60-957C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236126 | |||||||
| chr2:230236155 | G | A | 1 | a0005c0007t0001g0127 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.60-928G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236155 | |||||||
| chr2:230236164 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.60-919C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236164 | |||||||
| chr2:230236221 | C | A | 1 | a0002c0002t0001g0314 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.60-862C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236221 | |||||||
| chr2:230236265 | A | G | 1 | a0002c0002t0001g0332 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.60-818A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236265 | |||||||
| chr2:230236668 | C | T | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.60-415C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236668 | |||||||
| chr2:230236683 | C | T | 2 | a0002c0002t0001g0331 a0002c0002t0001g0334 |
2 | NA18965.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.60-400C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236683 | |||||||
| chr2:230236744 | C | T | 6 | a0004c0003t0001g0053 a0004c0003t0001g0229 a0004c0003t0001g0261 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.60-339C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236744 | |||||||
| chr2:230236834 | G | A | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.60-249G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236834 | |||||||
| chr2:230237720 | C | G | 6 | a0004c0003t0001g0053 a0004c0003t0001g0229 a0004c0003t0001g0261 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.237+460C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 2/26 | chr2 | 230237720 | |||||||
| chr2:230237833 | T | TA | 187 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(184): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.238-380_238-379ins others(1): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 2/26 | chr2 | 230237833 | |||||||
| chr2:230237973 | A | C | 3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.238-240A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 2/26 | chr2 | 230237973 | |||||||
| chr2:230238104 | C | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-109C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 2/26 | chr2 | 230238104 | |||||||
| chr2:230238402 | C | T | 1 | a0002c0002t0001g0339 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.406+21C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230238402 | |||||||
| chr2:230238470 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(192): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.406+89A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230238470 | |||||||
| chr2:230238493 | G | A | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.406+112G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230238493 | |||||||
| chr2:230238631 | G | A | 4 | a0006c0009t0002g0157 a0006c0009t0004g0158 a0006c0009t0004g0159 others(1): Show |
4 | HG02257.hp2 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+250G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230238631 | |||||||
| chr2:230238936 | G | A | 1 | a0007c0017t0001g0061 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.406+555G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230238936 | |||||||
| chr2:230238954 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.406+573G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230238954 | |||||||
| chr2:230238983 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.406+602A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230238983 | |||||||
| chr2:230239081 | A | T | 35 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(32): Show |
41 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.406+700A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239081 | |||||||
| chr2:230239099 | G | T | 5 | a0001c0001t0001g0156 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
5 | HG02723.hp2 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.406+718G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239099 | |||||||
| chr2:230239203 | C | T | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.406+822C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239203 | |||||||
| chr2:230239344 | T | A | 37 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(34): Show |
43 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.406+963T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239344 | |||||||
| chr2:230239348 | A | G | 3 | a0001c0001t0002g0003 a0001c0001t0002g0251 a0001c0001t0002g0252 |
5 | HG02717.hp2 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.406+967A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239348 | |||||||
| chr2:230239371 | T | C | 33 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(30): Show |
37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.406+990T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239371 | |||||||
| chr2:230239418 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | NA18946.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.406+1037A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239418 | |||||||
| chr2:230239645 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(178): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.406+1264C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239645 | |||||||
| chr2:230239677 | G | A | 1 | a0001c0001t0002g0230 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.406+1296G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239677 | |||||||
| chr2:230239764 | C | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(178): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.406+1383C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239764 | |||||||
| chr2:230239770 | T | C | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.406+1389T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239770 | |||||||
| chr2:230239775 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(178): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.406+1394C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239775 | |||||||
| chr2:230239901 | A | G | 1 | a0007c0017t0001g0061 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.407-1503A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239901 | |||||||
| chr2:230240019 | G | A | 1 | a0007c0017t0001g0061 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.407-1385G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240019 | |||||||
| chr2:230240043 | A | G | 1 | a0004c0003t0001g0304 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.407-1361A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240043 | |||||||
| chr2:230240092 | G | T | 1 | a0001c0001t0001g0195 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.407-1312G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240092 | |||||||
| chr2:230240129 | C | T | 2 | a0001c0006t0002g0007 a0001c0006t0002g0044 |
3 | HG03453.hp2 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.407-1275C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240129 | |||||||
| chr2:230240158 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 |
4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.407-1246A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240158 | |||||||
| chr2:230240216 | AAG | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(178): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.407-1184_407-1183d others(4): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 230240216 | ||||||
| chr2:230240357 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.407-1047C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240357 | |||||||
| chr2:230240380 | C | T | 33 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(30): Show |
37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.407-1024C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240380 | |||||||
| chr2:230240486 | A | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0148 |
2 | NA18975.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.407-918A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240486 | |||||||
| chr2:230240512 | A | G | 37 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(34): Show |
42 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.407-892A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240512 | |||||||
| chr2:230240555 | A | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(178): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.407-849A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240555 | |||||||
| chr2:230240568 | CATT | C | 27 | a0001c0001t0001g0019 a0001c0001t0001g0260 a0001c0001t0001g0266 others(24): Show |
28 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.407-831_407-829del others(3): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 230240568 | ||||||
| chr2:230240782 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.407-622A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240782 | |||||||
| chr2:230240897 | C | A | 2 | a0002c0002t0001g0315 a0002c0002t0001g0335 |
2 | NA18978.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.407-507C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240897 | |||||||
| chr2:230240931 | C | T | 21 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(18): Show |
24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.407-473C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240931 | |||||||
| chr2:230240939 | A | G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0193 a0001c0001t0002g0192 others(1): Show |
4 | NA18953.hp2 NA18979.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.407-465A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240939 | |||||||
| chr2:230241258 | C | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0297 a0001c0001t0001g0298 others(4): Show |
8 | HG01109.hp2 HG02572.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.407-146C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230241258 | |||||||
| chr2:230241271 | A | T | 1 | a0001c0001t0001g0310 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.407-133A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230241271 | |||||||
| chr2:230241372 | G | C | 1 | a0001c0006t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.407-32G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230241372 | |||||||
| chr2:230241514 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.490+27C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230241514 | |||||||
| chr2:230241529 | G | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(109): Show |
124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.490+42G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230241529 | |||||||
| chr2:230241567 | C | T | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+80C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230241567 | |||||||
| chr2:230241652 | G | T | 5 | a0001c0001t0001g0156 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
5 | HG02723.hp2 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+165G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230241652 | |||||||
| chr2:230241707 | A | G | 2 | a0009c0013t0001g0143 a0009c0013t0001g0144 |
2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.490+220A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230241707 | |||||||
| chr2:230241906 | A | G | 19 | a0004c0003t0001g0053 a0004c0003t0001g0229 a0004c0003t0001g0261 others(16): Show |
19 | HG00323.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.490+419A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230241906 | |||||||
| chr2:230242009 | C | T | 21 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(18): Show |
24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.490+522C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242009 | |||||||
| chr2:230242064 | G | T | 27 | a0001c0001t0001g0019 a0001c0001t0001g0260 a0001c0001t0001g0266 others(24): Show |
28 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.490+577G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242064 | |||||||
| chr2:230242143 | G | T | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+656G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242143 | |||||||
| chr2:230242220 | G | T | 21 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(18): Show |
24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.490+733G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242220 | |||||||
| chr2:230242229 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.490+742G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242229 | |||||||
| chr2:230242241 | ATAAAGAG others(25): Show |
A | 1 | a0001c0001t0001g0142 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.490+756_490+787del others(32): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr2 | 230242241 | ||||||
| chr2:230242270 | A | AT | 158 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(155): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.490+783_490+784ins others(1): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242270 | |||||||
| chr2:230242297 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.490+810G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242297 | |||||||
| chr2:230242339 | A | AGACAACT others(22): Show |
1 | a0001c0001t0001g0142 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.490+853_490+854ins others(29): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr2 | 230242339 | ||||||
| chr2:230242430 | G | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(155): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.490+943G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242430 | |||||||
| chr2:230242537 | C | T | 31 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0260 others(28): Show |
33 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.490+1050C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242537 | |||||||
| chr2:230242543 | T | C | 19 | a0004c0003t0001g0053 a0004c0003t0001g0229 a0004c0003t0001g0261 others(16): Show |
19 | HG00323.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.490+1056T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242543 | |||||||
| chr2:230242713 | T | C | 1 | a0002c0002t0001g0316 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.491-1018T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242713 | |||||||
| chr2:230242826 | C | G | 19 | a0004c0003t0001g0053 a0004c0003t0001g0229 a0004c0003t0001g0261 others(16): Show |
19 | HG00323.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.491-905C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242826 | |||||||
| chr2:230242876 | C | A | 1 | a0001c0006t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.491-855C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242876 | |||||||
| chr2:230243114 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(154): Show |
172 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.491-617G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243114 | |||||||
| chr2:230243238 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(135): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.491-493C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243238 | |||||||
| chr2:230243413 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.491-318A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243413 | |||||||
| chr2:230243456 | T | A | 15 | a0004c0003t0001g0053 a0004c0003t0001g0229 a0004c0003t0001g0261 others(12): Show |
15 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.491-275T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243456 | |||||||
| chr2:230243476 | A | G | 3 | a0003c0005t0003g0187 a0003c0005t0003g0188 a0003c0005t0003g0203 |
3 | HG01069.hp1 HG01071.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.491-255A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243476 | |||||||
| chr2:230243511 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.491-220A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243511 | |||||||
| chr2:230243523 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-208G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243523 | |||||||
| chr2:230243631 | A | T | 19 | a0004c0003t0001g0053 a0004c0003t0001g0229 a0004c0003t0001g0261 others(16): Show |
19 | HG00323.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.491-100A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243631 | |||||||
| chr2:230243725 | C | T | 9 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0302 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.491-6C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243725 | |||||||
| chr2:230244038 | A | T | 9 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0302 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.571+227A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244038 | |||||||
| chr2:230244195 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0140 |
2 | NA18962.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.571+384C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244195 | |||||||
| chr2:230244213 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(191): Show |
214 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.571+402T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244213 | |||||||
| chr2:230244222 | T | C | 1 | a0001c0006t0001g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.571+411T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244222 | |||||||
| chr2:230244553 | G | A | 35 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(32): Show |
41 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.572-435G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244553 | |||||||
| chr2:230244591 | C | A | 2 | a0009c0013t0001g0143 a0009c0013t0001g0144 |
2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.572-397C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244591 | |||||||
| chr2:230244614 | T | C | 47 | a0001c0001t0001g0156 a0001c0001t0001g0209 a0001c0001t0001g0210 others(44): Show |
50 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.572-374T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244614 | |||||||
| chr2:230244703 | G | GAAAAGA | 3 | a0002c0002t0001g0021 a0002c0002t0001g0315 a0002c0002t0001g0335 |
4 | NA18978.hp1 NA18982.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.572-278_572-273dup others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 230244703 | ||||||
| chr2:230244746 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 |
4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.572-242C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244746 | |||||||
| chr2:230244866 | C | T | 15 | a0004c0003t0001g0053 a0004c0003t0001g0229 a0004c0003t0001g0261 others(12): Show |
15 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.572-122C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244866 | |||||||
| chr2:230244918 | C | T | 1 | a0004c0003t0001g0340 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.572-70C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244918 | |||||||
| chr2:230244931 | T | A | 1 | a0001c0001t0002g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.572-57T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244931 | |||||||
| chr2:230244939 | G | T | 1 | a0001c0001t0002g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.572-49G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244939 | |||||||
| chr2:230244944 | T | C | 1 | a0003c0004t0003g0006 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.572-44T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244944 | |||||||
| chr2:230244972 | C | A | 1 | a0011c0014t0001g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.572-16C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244972 | |||||||
| chr2:230245125 | C | T | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.664+45C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/26 | chr2 | 230245125 | |||||||
| chr2:230245284 | G | T | 6 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG02486.hp2 HG02630.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.664+204G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/26 | chr2 | 230245284 | |||||||
| chr2:230245538 | G | A | 1 | a0001c0006t0002g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-325G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/26 | chr2 | 230245538 | |||||||
| chr2:230245692 | G | A | 2 | a0007c0012t0001g0024 a0007c0012t0001g0025 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.665-171G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/26 | chr2 | 230245692 | |||||||
| chr2:230245774 | C | G | 1 | a0002c0002t0001g0330 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.665-89C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/26 | chr2 | 230245774 | |||||||
| chr2:230245782 | G | A | 26 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(23): Show |
30 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.665-81G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/26 | chr2 | 230245782 | |||||||
| chr2:230245782 | G | T | 6 | a0004c0003t0001g0053 a0004c0003t0001g0229 a0004c0003t0001g0261 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-81G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/26 | chr2 | 230245782 | |||||||
| chr2:230246022 | C | T | 75 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(72): Show |
82 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.742+82C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246022 | |||||||
| chr2:230246074 | C | A | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.742+134C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246074 | |||||||
| chr2:230246268 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.742+328A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246268 | |||||||
| chr2:230246307 | C | T | 1 | a0001c0011t0001g0202 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.742+367C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246307 | |||||||
| chr2:230246308 | G | A | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.742+368G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246308 | |||||||
| chr2:230246348 | C | A | 75 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(72): Show |
82 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.742+408C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246348 | |||||||
| chr2:230246368 | T | C | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.742+428T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246368 | |||||||
| chr2:230246432 | C | T | 1 | a0003c0005t0003g0110 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.742+492C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246432 | |||||||
| chr2:230246707 | A | G | 81 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(78): Show |
88 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.742+767A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246707 | |||||||
| chr2:230247030 | C | T | 33 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(30): Show |
37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.743-886C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247030 | |||||||
| chr2:230247057 | C | G | 75 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(72): Show |
82 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.743-859C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247057 | |||||||
| chr2:230247116 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.743-800A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247116 | |||||||
| chr2:230247180 | C | T | 26 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(23): Show |
30 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.743-736C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247180 | |||||||
| chr2:230247309 | C | T | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-607C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247309 | |||||||
| chr2:230247390 | A | T | 81 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(78): Show |
88 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.743-526A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247390 | |||||||
| chr2:230247540 | C | T | 3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.743-376C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247540 | |||||||
| chr2:230247653 | G | A | 9 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0302 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.743-263G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247653 | |||||||
| chr2:230247661 | A | C | 1 | a0001c0001t0001g0109 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.743-255A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247661 | |||||||
| chr2:230248100 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0002g0208 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.892+35G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248100 | |||||||
| chr2:230248219 | A | G | 1 | a0011c0014t0001g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.892+154A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248219 | |||||||
| chr2:230248311 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.892+246A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248311 | |||||||
| chr2:230248481 | T | A | 1 | a0003c0004t0003g0006 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.893-404T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248481 | |||||||
| chr2:230248502 | A | T | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.893-383A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248502 | |||||||
| chr2:230248572 | A | C | 6 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG02486.hp2 HG02630.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.893-313A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248572 | |||||||
| chr2:230248663 | T | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
7 | HG01109.hp2 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.893-222T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248663 | |||||||
| chr2:230248690 | T | C | 81 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(78): Show |
88 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.893-195T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248690 | |||||||
| chr2:230248706 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.893-179C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248706 | |||||||
| chr2:230248719 | A | C | 1 | a0001c0006t0001g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.893-166A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248719 | |||||||
| chr2:230248784 | G | A | 23 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(20): Show |
26 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.893-101G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248784 | |||||||
| chr2:230248853 | C | T | 1 | a0001c0001t0002g0251 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.893-32C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248853 | |||||||
| chr2:230249062 | C | T | 5 | a0001c0001t0001g0274 a0001c0001t0001g0290 a0001c0001t0001g0291 others(2): Show |
5 | NA18957.hp1 NA18989.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.976+94C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249062 | |||||||
| chr2:230249195 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(192): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.976+227T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249195 | |||||||
| chr2:230249234 | C | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(72): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.976+266C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249234 | |||||||
| chr2:230249267 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.976+299C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249267 | |||||||
| chr2:230249287 | A | T | 1 | a0001c0001t0001g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.976+319A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249287 | |||||||
| chr2:230249408 | T | G | 8 | a0001c0001t0001g0065 a0001c0001t0001g0070 a0001c0001t0001g0109 others(5): Show |
8 | HG00558.hp1 HG01169.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.976+440T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249408 | |||||||
| chr2:230249416 | G | A | 29 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(26): Show |
32 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.976+448G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249416 | |||||||
| chr2:230249465 | A | G | 81 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(78): Show |
88 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.976+497A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249465 | |||||||
| chr2:230249624 | G | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(223): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.976+656G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249624 | |||||||
| chr2:230249738 | G | A | 79 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(76): Show |
86 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.976+770G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249738 | |||||||
| chr2:230249768 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(186): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.976+800G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249768 | |||||||
| chr2:230249878 | C | G | 73 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(70): Show |
80 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.976+910C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249878 | |||||||
| chr2:230249974 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.976+1006C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249974 | |||||||
| chr2:230250005 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.977-976T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250005 | |||||||
| chr2:230250028 | A | T | 1 | a0002c0002t0001g0313 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.977-953A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250028 | |||||||
| chr2:230250084 | A | G | 29 | a0001c0001t0001g0019 a0001c0001t0001g0260 a0001c0001t0001g0266 others(26): Show |
30 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.977-897A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250084 | |||||||
| chr2:230250092 | C | T | 52 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(49): Show |
56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.977-889C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250092 | |||||||
| chr2:230250167 | C | G | 6 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(3): Show |
6 | HG00639.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.977-814C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250167 | |||||||
| chr2:230250275 | C | G | 27 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(24): Show |
30 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.977-706C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250275 | |||||||
| chr2:230250280 | C | T | 27 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(24): Show |
30 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.977-701C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250280 | |||||||
| chr2:230250298 | A | G | 79 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(76): Show |
86 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.977-683A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250298 | |||||||
| chr2:230250481 | T | G | 79 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(76): Show |
86 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.977-500T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250481 | |||||||
| chr2:230250491 | C | T | 33 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(30): Show |
37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.977-490C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250491 | |||||||
| chr2:230250518 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.977-463A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250518 | |||||||
| chr2:230250530 | C | G | 1 | a0004c0003t0001g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.977-451C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250530 | |||||||
| chr2:230250558 | G | C | 6 | a0004c0003t0001g0053 a0004c0003t0001g0229 a0004c0003t0001g0261 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.977-423G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250558 | |||||||
| chr2:230250633 | G | A | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.977-348G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250633 | |||||||
| chr2:230250700 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.977-281A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250700 | |||||||
| chr2:230250739 | G | C | 21 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(18): Show |
24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.977-242G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250739 | |||||||
| chr2:230250743 | A | G | 8 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0123 others(5): Show |
8 | HG00140.hp2 HG01099.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.977-238A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250743 | |||||||
| chr2:230250809 | A | T | 35 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(32): Show |
41 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.977-172A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250809 | |||||||
| chr2:230250888 | T | C | 80 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(77): Show |
87 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.977-93T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250888 | |||||||
| chr2:230250915 | A | T | 28 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(25): Show |
31 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.977-66A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250915 | |||||||
| chr2:230251075 | G | A | 19 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(16): Show |
22 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1057+14G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251075 | |||||||
| chr2:230251170 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1057+109A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251170 | |||||||
| chr2:230251261 | C | T | 21 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(18): Show |
24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1057+200C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251261 | |||||||
| chr2:230251265 | A | G | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | HG01081.hp2 HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1057+204A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251265 | |||||||
| chr2:230251304 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1057+243C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251304 | |||||||
| chr2:230251442 | C | A | 52 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(49): Show |
56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1057+381C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251442 | |||||||
| chr2:230251508 | C | T | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1057+447C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251508 | |||||||
| chr2:230251645 | T | C | 37 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(34): Show |
41 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1057+584T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251645 | |||||||
| chr2:230251702 | T | A | 28 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(25): Show |
31 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1057+641T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251702 | |||||||
| chr2:230251805 | C | T | 1 | a0005c0007t0001g0010 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1057+744C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251805 | |||||||
| chr2:230251862 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(107): Show |
122 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1057+801C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251862 | |||||||
| chr2:230252080 | T | A | 9 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0302 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1057+1019T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252080 | |||||||
| chr2:230252159 | C | T | 21 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(18): Show |
24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1057+1098C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252159 | |||||||
| chr2:230252271 | A | G | 6 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(3): Show |
6 | HG00639.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058-1045A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252271 | |||||||
| chr2:230252396 | G | A | 33 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(30): Show |
37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1058-920G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252396 | |||||||
| chr2:230252418 | C | A | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1058-898C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252418 | |||||||
| chr2:230252421 | G | A | 31 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(28): Show |
37 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1058-895G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252421 | |||||||
| chr2:230252454 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1058-862G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252454 | |||||||
| chr2:230252751 | T | TAGAAAAG others(318): Show |
3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1058-548_1058-547i others(327): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 230252751 | ||||||
| chr2:230252770 | A | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(170): Show |
190 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1058-546A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252770 | |||||||
| chr2:230252800 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(169): Show |
189 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1058-516G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252800 | |||||||
| chr2:230252810 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(169): Show |
189 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1058-506G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252810 | |||||||
| chr2:230252812 | C | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(165): Show |
184 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1058-504C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252812 | |||||||
| chr2:230252832 | G | A | 49 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(46): Show |
53 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1058-484G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252832 | |||||||
| chr2:230252864 | G | T | 52 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(49): Show |
56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1058-452G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252864 | |||||||
| chr2:230252952 | C | T | 37 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(34): Show |
41 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1058-364C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252952 | |||||||
| chr2:230253049 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1058-267A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230253049 | |||||||
| chr2:230253155 | C | T | 6 | a0004c0003t0001g0053 a0004c0003t0001g0229 a0004c0003t0001g0261 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1058-161C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230253155 | |||||||
| chr2:230253156 | G | A | 2 | a0001c0001t0002g0236 a0001c0001t0002g0247 |
2 | HG00642.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1058-160G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230253156 | |||||||
| chr2:230253209 | A | G | 1 | a0013c0015t0001g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1058-107A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230253209 | |||||||
| chr2:230253286 | G | A | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1058-30G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230253286 | |||||||
| chr2:230253432 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1159+15C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230253432 | |||||||
| chr2:230253471 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(72): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1159+54G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230253471 | |||||||
| chr2:230253655 | C | G | 52 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(49): Show |
56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1159+238C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230253655 | |||||||
| chr2:230253727 | C | T | 52 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(49): Show |
56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1159+310C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230253727 | |||||||
| chr2:230253832 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0063 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1159+415G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230253832 | |||||||
| chr2:230253947 | T | G | 1 | a0002c0008t0001g0317 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1159+530T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230253947 | |||||||
| chr2:230254050 | A | G | 5 | a0004c0003t0001g0053 a0004c0003t0001g0261 a0004c0003t0001g0262 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1159+633A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254050 | |||||||
| chr2:230254071 | C | G | 5 | a0004c0003t0001g0053 a0004c0003t0001g0261 a0004c0003t0001g0262 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1159+654C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254071 | |||||||
| chr2:230254169 | A | G | 1 | a0001c0001t0002g0271 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1159+752A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254169 | |||||||
| chr2:230254177 | A | G | 1 | a0001c0001t0001g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1159+760A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254177 | |||||||
| chr2:230254185 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1159+768A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254185 | |||||||
| chr2:230254311 | A | G | 52 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(49): Show |
56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1159+894A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254311 | |||||||
| chr2:230254317 | A | G | 1 | a0002c0002t0001g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1159+900A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254317 | |||||||
| chr2:230254395 | C | A | 9 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0302 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1159+978C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254395 | |||||||
| chr2:230254549 | C | T | 52 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(49): Show |
56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1160-903C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254549 | |||||||
| chr2:230254848 | C | T | 1 | a0003c0004t0003g0028 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1160-604C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254848 | |||||||
| chr2:230254849 | A | G | 1 | a0003c0004t0003g0028 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1160-603A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254849 | |||||||
| chr2:230254952 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1160-500C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254952 | |||||||
| chr2:230254968 | T | G | 1 | a0001c0001t0001g0186 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1160-484T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254968 | |||||||
| chr2:230254984 | C | G | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1160-468C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254984 | |||||||
| chr2:230255075 | T | G | 1 | a0001c0001t0001g0186 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1160-377T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230255075 | |||||||
| chr2:230255199 | G | C | 22 | a0001c0001t0005g0126 a0001c0006t0001g0035 a0001c0006t0001g0036 others(19): Show |
25 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.1160-253G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230255199 | |||||||
| chr2:230255295 | G | A | 1 | a0013c0015t0001g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1160-157G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230255295 | |||||||
| chr2:230255327 | C | T | 4 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0195 others(1): Show |
4 | HG02148.hp1 HG02602.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-125C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230255327 | |||||||
| chr2:230255353 | G | A | 1 | a0002c0002t0001g0339 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1160-99G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230255353 | |||||||
| chr2:230255437 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1160-15C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230255437 | |||||||
| chr2:230255540 | CG | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(257): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1240+18delG | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230255540 | ||||||
| chr2:230255540 | CGG | C | 58 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0026 others(55): Show |
65 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1240+17_1240+18del others(2): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230255540 | ||||||
| chr2:230255542 | G | C | 4 | a0001c0001t0001g0213 a0003c0005t0003g0013 a0003c0005t0003g0218 others(1): Show |
5 | HG01175.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+10G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230255542 | |||||||
| chr2:230255543 | G | C | 11 | a0001c0001t0001g0049 a0001c0001t0001g0161 a0001c0001t0001g0163 others(8): Show |
11 | NA18940.hp2 NA18944.hp1 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.1240+11G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230255543 | |||||||
| chr2:230255543 | G | T | 51 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0026 others(48): Show |
58 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1240+11G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230255543 | |||||||
| chr2:230255544 | G | C | 2 | a0001c0001t0001g0228 a0003c0004t0010g0033 |
2 | HG06807.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1240+12G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230255544 | |||||||
| chr2:230255547 | G | A | 1 | a0002c0002t0001g0333 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1240+15G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230255547 | |||||||
| chr2:230255548 | G | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+16G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230255548 | |||||||
| chr2:230255549 | G | T | 1 | a0013c0015t0001g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1240+17G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230255549 | |||||||
| chr2:230256004 | C | T | 31 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(28): Show |
37 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1240+472C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256004 | |||||||
| chr2:230256031 | T | C | 340 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(337): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1240+499T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256031 | |||||||
| chr2:230256083 | A | C | 1 | a0004c0003t0001g0340 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1240+551A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256083 | |||||||
| chr2:230256287 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1240+755T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256287 | |||||||
| chr2:230256287 | T | G | 5 | a0004c0003t0001g0053 a0004c0003t0001g0261 a0004c0003t0001g0262 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+755T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256287 | |||||||
| chr2:230256344 | TA | T | 3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+818delA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230256344 | ||||||
| chr2:230256367 | TTTGTAGG others(2): Show |
T | 3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+836_1240+844d others(11): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256367 | |||||||
| chr2:230256380 | G | C | 3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+848G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256380 | |||||||
| chr2:230256381 | G | A | 3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+849G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256381 | |||||||
| chr2:230256382 | A | T | 3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+850A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256382 | |||||||
| chr2:230256383 | TGA | T | 3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+852_1240+853d others(4): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256383 | |||||||
| chr2:230256386 | A | T | 3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+854A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256386 | |||||||
| chr2:230256482 | T | C | 1 | a0002c0002t0001g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1240+950T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256482 | |||||||
| chr2:230256523 | T | G | 1 | a0001c0001t0001g0186 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1240+991T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256523 | |||||||
| chr2:230256528 | T | TG | 31 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(28): Show |
37 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1240+1001dupG | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230256528 | ||||||
| chr2:230256534 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1240+1002A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256534 | |||||||
| chr2:230256569 | G | A | 6 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0305 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+1037G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256569 | |||||||
| chr2:230256786 | G | T | 1 | a0001c0001t0002g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1240+1254G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256786 | |||||||
| chr2:230256791 | T | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0205 |
2 | HG01257.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1240+1259T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256791 | |||||||
| chr2:230256874 | G | T | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1240+1342G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256874 | |||||||
| chr2:230256913 | T | C | 6 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0305 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+1381T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256913 | |||||||
| chr2:230256965 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | NA18946.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1240+1433T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256965 | |||||||
| chr2:230257114 | T | C | 54 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(51): Show |
63 | HG00140.hp1 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1240+1582T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257114 | |||||||
| chr2:230257259 | C | T | 6 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0305 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+1727C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257259 | |||||||
| chr2:230257279 | C | A | 2 | a0003c0004t0003g0008 a0003c0004t0003g0040 |
3 | HG01169.hp1 HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1240+1747C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257279 | |||||||
| chr2:230257342 | T | G | 25 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(22): Show |
28 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1240+1810T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257342 | |||||||
| chr2:230257374 | CAGTA | C | 25 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(22): Show |
28 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1240+1845_1240+184 others(8): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230257374 | ||||||
| chr2:230257486 | G | A | 32 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(29): Show |
38 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.1240+1954G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257486 | |||||||
| chr2:230257495 | A | G | 58 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(55): Show |
67 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1240+1963A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257495 | |||||||
| chr2:230257575 | G | A | 112 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0026 others(109): Show |
126 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1240+2043G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257575 | |||||||
| chr2:230257650 | C | T | 1 | a0001c0001t0002g0245 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1240+2118C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257650 | |||||||
| chr2:230257703 | G | A | 4 | a0003c0005t0003g0166 a0003c0005t0003g0187 a0003c0005t0003g0188 others(1): Show |
4 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+2171G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257703 | |||||||
| chr2:230257706 | G | A | 2 | a0002c0002t0001g0318 a0002c0002t0001g0319 |
2 | HG01516.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1240+2174G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257706 | |||||||
| chr2:230257792 | C | G | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1240+2260C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257792 | |||||||
| chr2:230257801 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1240+2269A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257801 | |||||||
| chr2:230257833 | G | A | 7 | a0004c0003t0001g0267 a0004c0003t0001g0300 a0004c0003t0001g0301 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+2301G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257833 | |||||||
| chr2:230257910 | C | T | 6 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0305 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+2378C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257910 | |||||||
| chr2:230257919 | A | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0094 a0001c0001t0001g0095 |
4 | HG02040.hp2 NA18957.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+2387A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257919 | |||||||
| chr2:230258227 | T | G | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1240+2695T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258227 | |||||||
| chr2:230258429 | T | A | 7 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(4): Show |
7 | HG00639.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+2897T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258429 | |||||||
| chr2:230258527 | T | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0149 |
2 | NA18998.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1240+2995T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258527 | |||||||
| chr2:230258556 | T | C | 6 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0305 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+3024T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258556 | |||||||
| chr2:230258649 | T | G | 35 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(32): Show |
39 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1240+3117T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258649 | |||||||
| chr2:230258745 | A | C | 56 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0026 others(53): Show |
62 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1240+3213A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258745 | |||||||
| chr2:230258887 | A | C | 6 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0305 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+3355A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258887 | |||||||
| chr2:230258895 | G | T | 1 | a0001c0001t0001g0182 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1240+3363G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258895 | |||||||
| chr2:230258898 | C | CT | 17 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(14): Show |
18 | HG00639.hp2 HG01106.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1240+3378dupT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230258898 | ||||||
| chr2:230258937 | T | C | 11 | a0001c0001t0001g0023 a0001c0001t0001g0152 a0001c0001t0001g0156 others(8): Show |
12 | HG00639.hp2 HG02630.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1240+3405T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258937 | |||||||
| chr2:230259004 | A | G | 39 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(36): Show |
43 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1240+3472A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259004 | |||||||
| chr2:230259081 | GTTTA | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+3569_1240+357 others(8): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259081 | ||||||
| chr2:230259115 | G | A | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1240+3583G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259115 | |||||||
| chr2:230259194 | A | G | 4 | a0001c0001t0005g0126 a0007c0012t0001g0024 a0007c0012t0001g0025 others(1): Show |
4 | HG00323.hp2 HG01243.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+3662A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259194 | |||||||
| chr2:230259211 | C | T | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1240+3679C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259211 | |||||||
| chr2:230259398 | C | A | 1 | a0001c0001t0001g0342 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1240+3866C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259398 | |||||||
| chr2:230259405 | C | T | 1 | a0004c0003t0001g0337 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1240+3873C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259405 | |||||||
| chr2:230259430 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+3898C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259430 | |||||||
| chr2:230259506 | C | T | 7 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(4): Show |
7 | HG00639.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+3974C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259506 | |||||||
| chr2:230259512 | C | T | 1 | a0001c0001t0004g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1240+3980C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259512 | |||||||
| chr2:230259515 | TA | T | 25 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(22): Show |
28 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1240+3996delA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259515 | ||||||
| chr2:230259612 | G | A | 2 | a0001c0001t0001g0213 a0013c0015t0001g0308 |
2 | HG03486.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1240+4080G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259612 | |||||||
| chr2:230259617 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+4085G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259617 | |||||||
| chr2:230259673 | C | T | 14 | a0001c0001t0001g0065 a0001c0001t0001g0070 a0001c0001t0001g0115 others(11): Show |
14 | HG00558.hp1 HG01169.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1240+4141C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259673 | |||||||
| chr2:230259686 | C | CA | 35 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(32): Show |
41 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1240+4165dupA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259686 | ||||||
| chr2:230259686 | CA | C | 7 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0101 others(4): Show |
7 | HG02040.hp1 HG02080.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+4165delA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259686 | ||||||
| chr2:230259726 | A | G | 1 | a0001c0001t0002g0244 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1240+4194A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259726 | |||||||
| chr2:230259770 | TCATATAT others(20): Show |
T | 46 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(43): Show |
51 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1240+4241_1240+426 others(31): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259770 | ||||||
| chr2:230259771 | C | CAT | 88 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(85): Show |
97 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1240+4263_1240+426 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | ||||||
| chr2:230259771 | C | CATAT | 16 | a0001c0001t0001g0020 a0001c0001t0001g0177 a0001c0001t0001g0181 others(13): Show |
17 | HG01109.hp2 HG01123.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1240+4261_1240+426 others(8): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | ||||||
| chr2:230259771 | C | CATATAT | 5 | a0001c0001t0001g0214 a0001c0006t0001g0046 a0001c0006t0001g0047 others(2): Show |
5 | HG01361.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+4259_1240+426 others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | ||||||
| chr2:230259771 | C | CATATATA others(3): Show |
1 | a0013c0015t0001g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1240+4255_1240+426 others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | ||||||
| chr2:230259771 | C | CATATATA others(5): Show |
3 | a0001c0001t0001g0201 a0001c0001t0001g0204 a0001c0001t0001g0342 |
3 | HG03490.hp1 HG03492.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1240+4253_1240+426 others(16): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | ||||||
| chr2:230259771 | C | CATATATA others(7): Show |
9 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0226 others(6): Show |
9 | HG00735.hp2 HG02074.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+4251_1240+426 others(18): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | ||||||
| chr2:230259771 | C | CATATATA others(9): Show |
17 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0001g0274 others(14): Show |
18 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1240+4249_1240+426 others(20): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | ||||||
| chr2:230259771 | C | CATATATA others(11): Show |
12 | a0001c0001t0001g0195 a0001c0001t0001g0206 a0001c0001t0001g0307 others(9): Show |
12 | HG00140.hp1 HG01099.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1240+4247_1240+426 others(22): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | ||||||
| chr2:230259771 | C | CATATATA others(13): Show |
13 | a0001c0001t0001g0023 a0001c0001t0001g0196 a0001c0001t0001g0281 others(10): Show |
15 | HG00323.hp2 HG00639.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+4245_1240+426 others(24): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | ||||||
| chr2:230259771 | C | CATATATA others(15): Show |
3 | a0001c0006t0001g0039 a0003c0004t0003g0031 a0007c0012t0001g0025 |
3 | HG00738.hp2 HG01358.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+4243_1240+426 others(26): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | ||||||
| chr2:230259771 | C | CATATATA others(17): Show |
7 | a0001c0001t0001g0286 a0001c0001t0001g0296 a0001c0006t0001g0045 others(4): Show |
7 | HG00323.hp1 HG01433.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+4241_1240+426 others(28): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | ||||||
| chr2:230259771 | C | CATATATA others(19): Show |
1 | a0001c0006t0001g0037 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1240+4264_1240+426 others(30): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | ||||||
| chr2:230259771 | C | CATATATA others(21): Show |
7 | a0001c0001t0001g0277 a0001c0001t0001g0287 a0003c0004t0003g0040 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+4264_1240+426 others(32): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | ||||||
| chr2:230259771 | C | CATATATA others(23): Show |
4 | a0001c0006t0002g0007 a0001c0006t0002g0044 a0003c0004t0003g0008 others(1): Show |
5 | HG01123.hp1 HG01169.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+4264_1240+426 others(34): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | ||||||
| chr2:230259805 | A | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+4273A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259805 | |||||||
| chr2:230259847 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+4315G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259847 | |||||||
| chr2:230259856 | G | C | 5 | a0004c0003t0001g0053 a0004c0003t0001g0261 a0004c0003t0001g0262 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+4324G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259856 | |||||||
| chr2:230259959 | G | C | 46 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(43): Show |
51 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1240+4427G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259959 | |||||||
| chr2:230260037 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1240+4505G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260037 | |||||||
| chr2:230260060 | C | T | 1 | a0004c0003t0001g0304 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1240+4528C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260060 | |||||||
| chr2:230260061 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+4529A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260061 | |||||||
| chr2:230260112 | T | A | 40 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(37): Show |
46 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1240+4580T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260112 | |||||||
| chr2:230260134 | C | A | 5 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG02486.hp2 HG03209.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+4602C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260134 | |||||||
| chr2:230260147 | G | T | 39 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(36): Show |
44 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1240+4615G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260147 | |||||||
| chr2:230260158 | T | C | 2 | a0001c0001t0002g0234 a0001c0001t0002g0237 |
2 | HG01069.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1240+4626T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260158 | |||||||
| chr2:230260188 | T | C | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1240+4656T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260188 | |||||||
| chr2:230260311 | T | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+4779T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260311 | |||||||
| chr2:230260369 | A | G | 2 | a0003c0004t0003g0008 a0003c0004t0003g0040 |
3 | HG01169.hp1 HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1240+4837A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260369 | |||||||
| chr2:230260520 | G | A | 9 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(6): Show |
9 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+4988G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260520 | |||||||
| chr2:230260781 | G | A | 84 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0023 others(81): Show |
96 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1240+5249G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260781 | |||||||
| chr2:230260814 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1240+5282C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260814 | |||||||
| chr2:230260870 | G | A | 38 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(35): Show |
43 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1240+5338G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260870 | |||||||
| chr2:230260872 | G | C | 40 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(37): Show |
46 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1240+5340G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260872 | |||||||
| chr2:230260972 | T | G | 47 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(44): Show |
52 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1240+5440T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260972 | |||||||
| chr2:230260987 | T | C | 47 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(44): Show |
52 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1240+5455T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260987 | |||||||
| chr2:230261105 | A | G | 7 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(4): Show |
7 | HG00639.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+5573A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261105 | |||||||
| chr2:230261265 | G | A | 35 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(32): Show |
41 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1240+5733G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261265 | |||||||
| chr2:230261547 | G | A | 3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+6015G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261547 | |||||||
| chr2:230261612 | C | A | 80 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0241 others(77): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1240+6080C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261612 | |||||||
| chr2:230261725 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1240+6193T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261725 | |||||||
| chr2:230261727 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1240+6195T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261727 | |||||||
| chr2:230261813 | G | A | 24 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(21): Show |
27 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1240+6281G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261813 | |||||||
| chr2:230261819 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1240+6287G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261819 | |||||||
| chr2:230261848 | A | C | 3 | a0001c0006t0002g0007 a0001c0006t0002g0044 a0003c0004t0010g0033 |
4 | HG03453.hp2 HG03516.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+6316A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261848 | |||||||
| chr2:230261923 | C | T | 79 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0241 others(76): Show |
90 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1240+6391C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261923 | |||||||
| chr2:230261924 | T | C | 1 | a0004c0003t0001g0300 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1240+6392T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261924 | |||||||
| chr2:230261934 | C | T | 5 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG02486.hp2 HG03209.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+6402C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261934 | |||||||
| chr2:230262000 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+6468A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262000 | |||||||
| chr2:230262279 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1240+6747C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262279 | |||||||
| chr2:230262397 | C | G | 6 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0305 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+6865C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262397 | |||||||
| chr2:230262413 | C | T | 6 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0305 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+6881C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262413 | |||||||
| chr2:230262511 | G | A | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1240+6979G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262511 | |||||||
| chr2:230262563 | A | G | 36 | a0001c0001t0001g0019 a0001c0001t0001g0183 a0001c0001t0001g0185 others(33): Show |
37 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.1241-6969A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262563 | |||||||
| chr2:230262578 | G | A | 3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1241-6954G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262578 | |||||||
| chr2:230262667 | A | G | 1 | a0011c0014t0001g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1241-6865A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262667 | |||||||
| chr2:230262705 | C | T | 1 | a0004c0003t0001g0305 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1241-6827C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262705 | |||||||
| chr2:230262718 | A | G | 32 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(29): Show |
38 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.1241-6814A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262718 | |||||||
| chr2:230262911 | G | C | 2 | a0004c0003t0001g0302 a0004c0003t0001g0303 |
2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1241-6621G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262911 | |||||||
| chr2:230262960 | T | C | 1 | a0003c0004t0003g0006 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1241-6572T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262960 | |||||||
| chr2:230263009 | A | T | 1 | a0001c0001t0001g0342 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1241-6523A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263009 | |||||||
| chr2:230263172 | G | A | 35 | a0001c0001t0001g0056 a0002c0002t0001g0004 a0002c0002t0001g0021 others(32): Show |
39 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1241-6360G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263172 | |||||||
| chr2:230263202 | G | A | 2 | a0001c0001t0001g0200 a0004c0003t0001g0267 |
2 | HG00280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1241-6330G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263202 | |||||||
| chr2:230263279 | C | A | 1 | a0003c0005t0003g0013 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1241-6253C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263279 | |||||||
| chr2:230263346 | G | A | 35 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(32): Show |
41 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1241-6186G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263346 | |||||||
| chr2:230263464 | T | C | 44 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0026 others(41): Show |
50 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1241-6068T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263464 | |||||||
| chr2:230263716 | C | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1241-5816C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263716 | |||||||
| chr2:230263808 | C | T | 79 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0241 others(76): Show |
90 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1241-5724C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263808 | |||||||
| chr2:230263911 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1241-5621T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263911 | |||||||
| chr2:230263942 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1241-5590T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263942 | |||||||
| chr2:230263952 | C | T | 1 | a0002c0002t0001g0333 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1241-5580C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263952 | |||||||
| chr2:230264700 | G | T | 3 | a0001c0006t0002g0007 a0001c0006t0002g0044 a0003c0004t0010g0033 |
4 | HG03453.hp2 HG03516.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-4832G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230264700 | |||||||
| chr2:230264748 | G | T | 1 | a0008c0010t0001g0117 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1241-4784G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230264748 | |||||||
| chr2:230264760 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1241-4772C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230264760 | |||||||
| chr2:230264874 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1241-4658G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230264874 | |||||||
| chr2:230265014 | C | G | 76 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0026 others(73): Show |
86 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.1241-4518C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265014 | |||||||
| chr2:230265015 | A | G | 124 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0023 others(121): Show |
139 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1241-4517A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265015 | |||||||
| chr2:230265079 | C | T | 31 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(28): Show |
34 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1241-4453C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265079 | |||||||
| chr2:230265101 | G | C | 35 | a0001c0001t0005g0126 a0002c0002t0001g0004 a0002c0002t0001g0021 others(32): Show |
39 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1241-4431G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265101 | |||||||
| chr2:230265123 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-4409G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265123 | |||||||
| chr2:230265162 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1241-4370G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265162 | |||||||
| chr2:230265442 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1241-4090G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265442 | |||||||
| chr2:230265459 | G | A | 6 | a0001c0001t0001g0266 a0001c0001t0001g0274 a0001c0001t0001g0290 others(3): Show |
6 | NA18957.hp1 NA18986.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.1241-4073G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265459 | |||||||
| chr2:230265468 | G | A | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1241-4064G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265468 | |||||||
| chr2:230265585 | T | G | 52 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0023 others(49): Show |
60 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1241-3947T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265585 | |||||||
| chr2:230265723 | G | T | 1 | a0001c0001t0001g0293 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1241-3809G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265723 | |||||||
| chr2:230265790 | CG | C | 100 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0152 others(97): Show |
114 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1241-3733delG | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230265790 | ||||||
| chr2:230265793 | G | T | 24 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(21): Show |
27 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1241-3739G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265793 | |||||||
| chr2:230265794 | G | GT | 45 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0183 others(42): Show |
47 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.1241-3738_1241-373 others(5): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265794 | |||||||
| chr2:230265837 | C | A | 3 | a0001c0001t0001g0167 a0001c0001t0001g0186 a0001c0001t0001g0220 |
3 | NA18949.hp2 NA18983.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1241-3695C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265837 | |||||||
| chr2:230265874 | G | A | 2 | a0009c0013t0001g0143 a0009c0013t0001g0144 |
2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1241-3658G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265874 | |||||||
| chr2:230266012 | T | C | 32 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(29): Show |
38 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.1241-3520T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266012 | |||||||
| chr2:230266172 | C | T | 121 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0023 others(118): Show |
136 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1241-3360C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266172 | |||||||
| chr2:230266246 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1241-3286G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266246 | |||||||
| chr2:230266306 | A | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0023 others(52): Show |
63 | HG00423.hp1 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1241-3226A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266306 | |||||||
| chr2:230266360 | A | G | 5 | a0004c0003t0001g0053 a0004c0003t0001g0261 a0004c0003t0001g0262 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-3172A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266360 | |||||||
| chr2:230266431 | A | G | 36 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0241 others(33): Show |
43 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.1241-3101A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266431 | |||||||
| chr2:230266611 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1241-2921C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266611 | |||||||
| chr2:230266659 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1241-2873C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266659 | |||||||
| chr2:230266672 | G | A | 24 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(21): Show |
27 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1241-2860G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266672 | |||||||
| chr2:230266806 | A | G | 37 | a0001c0001t0001g0019 a0001c0001t0001g0183 a0001c0001t0001g0185 others(34): Show |
38 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1241-2726A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266806 | |||||||
| chr2:230266894 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1241-2638A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266894 | |||||||
| chr2:230266988 | C | G | 5 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG02486.hp2 HG03209.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1241-2544C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266988 | |||||||
| chr2:230267029 | C | G | 2 | a0003c0005t0003g0105 a0003c0005t0003g0110 |
2 | HG00140.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1241-2503C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267029 | |||||||
| chr2:230267030 | T | G | 2 | a0003c0005t0003g0105 a0003c0005t0003g0110 |
2 | HG00140.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1241-2502T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267030 | |||||||
| chr2:230267200 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1241-2332T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267200 | |||||||
| chr2:230267382 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1241-2150T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267382 | |||||||
| chr2:230267435 | G | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0252 |
4 | HG02717.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-2097G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267435 | |||||||
| chr2:230267526 | G | C | 6 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0230 others(3): Show |
9 | HG00423.hp1 NA18943.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.1241-2006G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267526 | |||||||
| chr2:230267702 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1241-1830G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267702 | |||||||
| chr2:230267844 | T | G | 2 | a0001c0001t0001g0341 a0004c0003t0001g0229 |
2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1241-1688T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267844 | |||||||
| chr2:230267885 | A | T | 14 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(11): Show |
14 | HG02055.hp2 HG02257.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1241-1647A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267885 | |||||||
| chr2:230267908 | A | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(35): Show |
43 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1241-1624A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267908 | |||||||
| chr2:230268006 | C | T | 3 | a0003c0004t0003g0041 a0003c0004t0003g0042 a0003c0004t0003g0043 |
3 | HG01123.hp1 HG01433.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1241-1526C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268006 | |||||||
| chr2:230268245 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1241-1287C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268245 | |||||||
| chr2:230268279 | T | C | 1 | a0001c0001t0002g0238 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1241-1253T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268279 | |||||||
| chr2:230268406 | C | G | 6 | a0001c0001t0001g0266 a0001c0001t0001g0274 a0001c0001t0001g0290 others(3): Show |
6 | NA18957.hp1 NA18986.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.1241-1126C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268406 | |||||||
| chr2:230268450 | A | G | 97 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0026 others(94): Show |
111 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1241-1082A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268450 | |||||||
| chr2:230268524 | T | TA | 10 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(7): Show |
10 | HG00639.hp2 HG02630.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-993dupA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230268524 | ||||||
| chr2:230268663 | T | A | 1 | a0001c0001t0002g0051 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1241-869T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268663 | |||||||
| chr2:230268813 | T | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(35): Show |
43 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1241-719T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268813 | |||||||
| chr2:230268863 | C | T | 3 | a0003c0004t0003g0030 a0003c0004t0003g0031 a0003c0004t0003g0032 |
3 | HG00738.hp2 HG01496.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1241-669C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268863 | |||||||
| chr2:230269144 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-388A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230269144 | |||||||
| chr2:230269363 | AGCGTG | A | 24 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(21): Show |
27 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1241-166_1241-162d others(7): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230269363 | ||||||
| chr2:230270395 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1445-191T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 14/26 | chr2 | 230270395 | |||||||
| chr2:230270852 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1498+213A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230270852 | |||||||
| chr2:230270947 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(74): Show |
83 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1498+308A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230270947 | |||||||
| chr2:230271350 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1498+711G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271350 | |||||||
| chr2:230271362 | G | C | 5 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG02486.hp2 HG03209.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+723G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271362 | |||||||
| chr2:230271372 | G | A | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1498+733G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271372 | |||||||
| chr2:230271442 | G | A | 1 | a0007c0017t0001g0061 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1498+803G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271442 | |||||||
| chr2:230271644 | G | A | 2 | a0003c0004t0003g0008 a0003c0004t0003g0040 |
3 | HG01169.hp1 HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1498+1005G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271644 | |||||||
| chr2:230271686 | G | A | 4 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0305 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1498+1047G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271686 | |||||||
| chr2:230271912 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+1273G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271912 | |||||||
| chr2:230271958 | T | A | 1 | a0001c0001t0001g0306 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1498+1319T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271958 | |||||||
| chr2:230272248 | G | C | 1 | a0001c0006t0001g0045 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1498+1609G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230272248 | |||||||
| chr2:230272303 | C | T | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1498+1664C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230272303 | |||||||
| chr2:230272446 | G | A | 5 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0311 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+1807G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230272446 | |||||||
| chr2:230272627 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0140 |
2 | NA18962.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1498+1988A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230272627 | |||||||
| chr2:230272834 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0142 |
2 | NA18981.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1498+2195G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230272834 | |||||||
| chr2:230273328 | C | A | 5 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0311 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+2689C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230273328 | |||||||
| chr2:230273368 | G | A | 5 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0311 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+2729G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230273368 | |||||||
| chr2:230273489 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1498+2850C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230273489 | |||||||
| chr2:230273530 | C | T | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1498+2891C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230273530 | |||||||
| chr2:230273649 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1498+3010A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230273649 | |||||||
| chr2:230273830 | A | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0293 |
2 | HG03017.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1498+3191A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230273830 | |||||||
| chr2:230274041 | T | C | 10 | a0001c0001t0004g0250 a0001c0001t0004g0312 a0004c0003t0001g0302 others(7): Show |
10 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1498+3402T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274041 | |||||||
| chr2:230274094 | T | G | 2 | a0009c0013t0001g0143 a0009c0013t0001g0144 |
2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1498+3455T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274094 | |||||||
| chr2:230274111 | TA | T | 61 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0026 others(58): Show |
68 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1498+3487delA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 230274111 | ||||||
| chr2:230274111 | TAA | T | 56 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(53): Show |
63 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.1498+3486_1498+348 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 230274111 | ||||||
| chr2:230274478 | T | C | 3 | a0001c0001t0004g0250 a0001c0001t0004g0312 a0012c0018t0001g0249 |
3 | HG02572.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1498+3839T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274478 | |||||||
| chr2:230274610 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0006g0093 |
2 | NA18951.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1498+3971C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274610 | |||||||
| chr2:230274645 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1498+4006G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274645 | |||||||
| chr2:230274655 | A | T | 1 | a0001c0001t0002g0243 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1498+4016A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274655 | |||||||
| chr2:230274664 | A | T | 1 | a0002c0002t0001g0328 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1498+4025A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274664 | |||||||
| chr2:230274667 | C | T | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1498+4028C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274667 | |||||||
| chr2:230274792 | T | G | 3 | a0007c0012t0001g0024 a0007c0012t0001g0025 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1498+4153T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274792 | |||||||
| chr2:230274803 | C | T | 7 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0209 others(4): Show |
7 | HG00639.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1498+4164C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274803 | |||||||
| chr2:230275062 | T | C | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1498+4423T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275062 | |||||||
| chr2:230275070 | G | A | 1 | a0005c0007t0001g0127 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1498+4431G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275070 | |||||||
| chr2:230275199 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498+4560T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275199 | |||||||
| chr2:230275305 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498+4666G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275305 | |||||||
| chr2:230275307 | C | CA | 31 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(28): Show |
37 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1498+4675dupA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 230275307 | ||||||
| chr2:230275342 | A | G | 2 | a0003c0004t0003g0008 a0003c0004t0003g0040 |
3 | HG01169.hp1 HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1498+4703A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275342 | |||||||
| chr2:230275350 | AC | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+4712delC | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275350 | |||||||
| chr2:230275497 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1498+4858G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275497 | |||||||
| chr2:230275505 | T | C | 9 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(6): Show |
9 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1498+4866T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275505 | |||||||
| chr2:230275546 | C | A | 1 | a0007c0012t0001g0024 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1498+4907C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275546 | |||||||
| chr2:230275785 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1498+5146A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275785 | |||||||
| chr2:230275859 | G | T | 2 | a0002c0002t0001g0329 a0008c0019t0001g0034 |
2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1498+5220G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275859 | |||||||
| chr2:230275968 | G | A | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1498+5329G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275968 | |||||||
| chr2:230276452 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1498+5813T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230276452 | |||||||
| chr2:230276481 | C | G | 28 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(25): Show |
32 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1498+5842C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230276481 | |||||||
| chr2:230276646 | AAC | A | 31 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(28): Show |
37 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1498+6011_1498+601 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 230276646 | ||||||
| chr2:230276773 | A | T | 1 | a0001c0001t0002g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1498+6134A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230276773 | |||||||
| chr2:230276857 | C | G | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1498+6218C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230276857 | |||||||
| chr2:230276938 | T | C | 6 | a0001c0001t0001g0064 a0001c0001t0001g0075 a0001c0001t0001g0076 others(3): Show |
6 | HG00673.hp2 HG02015.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.1498+6299T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230276938 | |||||||
| chr2:230277260 | C | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498+6621C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230277260 | |||||||
| chr2:230277350 | A | G | 6 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0305 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1498+6711A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230277350 | |||||||
| chr2:230277382 | T | C | 1 | a0011c0014t0001g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1498+6743T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230277382 | |||||||
| chr2:230277427 | C | T | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1498+6788C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230277427 | |||||||
| chr2:230277565 | A | C | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 |
3 | HG03130.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1499-6781A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230277565 | |||||||
| chr2:230277804 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1499-6542G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230277804 | |||||||
| chr2:230278274 | G | A | 1 | a0001c0001t0001g0307 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1499-6072G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278274 | |||||||
| chr2:230278514 | A | T | 1 | a0001c0001t0001g0266 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1499-5832A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278514 | |||||||
| chr2:230278573 | C | G | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1499-5773C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278573 | |||||||
| chr2:230278607 | C | G | 1 | a0001c0001t0002g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1499-5739C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278607 | |||||||
| chr2:230278731 | T | A | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1499-5615T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278731 | |||||||
| chr2:230278785 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1499-5561C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278785 | |||||||
| chr2:230278924 | C | T | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1499-5422C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278924 | |||||||
| chr2:230278985 | G | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0228 |
2 | HG01361.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1499-5361G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278985 | |||||||
| chr2:230279260 | A | G | 2 | a0001c0001t0002g0236 a0001c0001t0002g0247 |
2 | HG00642.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1499-5086A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230279260 | |||||||
| chr2:230279388 | G | C | 1 | a0008c0019t0001g0034 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1499-4958G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230279388 | |||||||
| chr2:230279513 | T | C | 4 | a0002c0002t0001g0153 a0002c0002t0001g0314 a0002c0002t0001g0316 others(1): Show |
4 | HG00408.hp2 HG01934.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1499-4833T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230279513 | |||||||
| chr2:230279838 | A | G | 101 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0026 others(98): Show |
115 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1499-4508A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230279838 | |||||||
| chr2:230279863 | TCCTCCTG | T | 34 | a0001c0001t0001g0019 a0001c0001t0001g0183 a0001c0001t0001g0185 others(31): Show |
35 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1499-4478_1499-447 others(11): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 230279863 | ||||||
| chr2:230280114 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1499-4232G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280114 | |||||||
| chr2:230280220 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1499-4126A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280220 | |||||||
| chr2:230280233 | AT | A | 5 | a0004c0003t0001g0053 a0004c0003t0001g0261 a0004c0003t0001g0262 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1499-4112delT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280233 | |||||||
| chr2:230280287 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1499-4059G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280287 | |||||||
| chr2:230280363 | C | T | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1499-3983C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280363 | |||||||
| chr2:230280458 | G | C | 1 | a0001c0001t0001g0146 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1499-3888G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280458 | |||||||
| chr2:230280469 | A | G | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1499-3877A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280469 | |||||||
| chr2:230280478 | C | A | 5 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0210 others(2): Show |
5 | HG00639.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1499-3868C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280478 | |||||||
| chr2:230280532 | C | T | 4 | a0003c0005t0003g0166 a0003c0005t0003g0187 a0003c0005t0003g0188 others(1): Show |
4 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1499-3814C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280532 | |||||||
| chr2:230280713 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1499-3633G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280713 | |||||||
| chr2:230280793 | C | T | 31 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(28): Show |
37 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1499-3553C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280793 | |||||||
| chr2:230280950 | T | C | 1 | a0002c0002t0001g0314 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1499-3396T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280950 | |||||||
| chr2:230281160 | G | A | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1499-3186G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230281160 | |||||||
| chr2:230281710 | T | A | 1 | a0001c0001t0001g0200 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1499-2636T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230281710 | |||||||
| chr2:230282313 | G | A | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1499-2033G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230282313 | |||||||
| chr2:230282354 | C | T | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1499-1992C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230282354 | |||||||
| chr2:230282528 | G | A | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1499-1818G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230282528 | |||||||
| chr2:230282618 | T | C | 159 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0018 others(156): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1499-1728T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230282618 | |||||||
| chr2:230282674 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | NA18944.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1499-1672C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230282674 | |||||||
| chr2:230282809 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1499-1537G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230282809 | |||||||
| chr2:230282809 | G | C | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1499-1537G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230282809 | |||||||
| chr2:230283060 | C | T | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1499-1286C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283060 | |||||||
| chr2:230283168 | G | A | 6 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0305 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499-1178G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283168 | |||||||
| chr2:230283196 | C | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(246): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1499-1150C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283196 | |||||||
| chr2:230283222 | A | G | 6 | a0004c0003t0001g0300 a0004c0003t0001g0301 a0004c0003t0001g0305 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499-1124A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283222 | |||||||
| chr2:230283294 | A | G | 37 | a0001c0001t0001g0019 a0001c0001t0001g0183 a0001c0001t0001g0185 others(34): Show |
38 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1499-1052A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283294 | |||||||
| chr2:230283413 | A | G | 27 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(24): Show |
30 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1499-933A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283413 | |||||||
| chr2:230283560 | G | A | 4 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0210 others(1): Show |
4 | HG00639.hp2 HG02723.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1499-786G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283560 | |||||||
| chr2:230283751 | A | G | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1499-595A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283751 | |||||||
| chr2:230283766 | A | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1499-580A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283766 | |||||||
| chr2:230283795 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1499-551C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283795 | |||||||
| chr2:230284023 | A | T | 1 | a0002c0002t0001g0330 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1499-323A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230284023 | |||||||
| chr2:230284064 | A | C | 39 | a0001c0001t0001g0018 a0001c0001t0001g0152 a0001c0001t0001g0156 others(36): Show |
45 | HG00423.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1499-282A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230284064 | |||||||
| chr2:230284123 | G | A | 31 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(28): Show |
37 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1499-223G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230284123 | |||||||
| chr2:230284172 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1499-174G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230284172 | |||||||
| chr2:230284173 | G | T | 1 | a0001c0001t0001g0019 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1499-173G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230284173 | |||||||
| chr2:230284181 | T | G | 1 | a0001c0001t0001g0019 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1499-165T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230284181 | |||||||
| chr2:230284182 | A | G | 1 | a0001c0001t0001g0019 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1499-164A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230284182 | |||||||
| chr2:230284510 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0123 |
2 | HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1564+99T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230284510 | |||||||
| chr2:230284655 | C | T | 2 | a0002c0002t0001g0153 a0002c0002t0001g0320 |
2 | HG01934.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1564+244C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230284655 | |||||||
| chr2:230284834 | A | G | 37 | a0001c0001t0001g0019 a0001c0001t0001g0183 a0001c0001t0001g0185 others(34): Show |
38 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1564+423A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230284834 | |||||||
| chr2:230284856 | A | G | 1 | a0001c0006t0001g0039 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1564+445A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230284856 | |||||||
| chr2:230284924 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1564+513T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230284924 | |||||||
| chr2:230285252 | C | G | 10 | a0001c0001t0004g0250 a0001c0001t0004g0312 a0004c0003t0001g0302 others(7): Show |
10 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1565-500C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230285252 | |||||||
| chr2:230285337 | T | C | 47 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0183 others(44): Show |
49 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.1565-415T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230285337 | |||||||
| chr2:230285378 | G | A | 2 | a0001c0001t0001g0341 a0004c0003t0001g0229 |
2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1565-374G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230285378 | |||||||
| chr2:230285433 | G | A | 1 | a0001c0001t0001g0012 | 2 | NA18957.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1565-319G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230285433 | |||||||
| chr2:230285676 | C | T | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1565-76C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230285676 | |||||||
| chr2:230285683 | G | A | 5 | a0004c0003t0001g0053 a0004c0003t0001g0261 a0004c0003t0001g0262 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565-69G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230285683 | |||||||
| chr2:230285851 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1645+19G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230285851 | |||||||
| chr2:230285934 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1645+102G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230285934 | |||||||
| chr2:230285969 | G | T | 5 | a0001c0001t0004g0250 a0001c0001t0004g0312 a0004c0003t0001g0302 others(2): Show |
5 | HG02572.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1645+137G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230285969 | |||||||
| chr2:230286091 | C | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0023 others(104): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1645+259C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286091 | |||||||
| chr2:230286138 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1645+306G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286138 | |||||||
| chr2:230286216 | C | T | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1645+384C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286216 | |||||||
| chr2:230286231 | T | C | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1645+399T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286231 | |||||||
| chr2:230286263 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1645+431T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286263 | |||||||
| chr2:230286292 | A | C | 2 | a0001c0001t0002g0242 a0001c0001t0002g0244 |
2 | HG02109.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1645+460A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286292 | |||||||
| chr2:230286295 | A | G | 5 | a0001c0001t0001g0068 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
5 | NA18956.hp2 NA19063.hp2 NA19082.hp1 others(2): Show |
intron_variant | MODIFIER | c.1645+463A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286295 | |||||||
| chr2:230286300 | T | C | 4 | a0001c0001t0002g0208 a0001c0001t0002g0242 a0001c0001t0002g0243 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1645+468T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286300 | |||||||
| chr2:230286398 | T | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0094 |
2 | HG02040.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1645+566T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286398 | |||||||
| chr2:230286431 | G | A | 1 | a0001c0001t0002g0238 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1645+599G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286431 | |||||||
| chr2:230286491 | G | A | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1645+659G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286491 | |||||||
| chr2:230287028 | C | T | 139 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(136): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1646-864C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287028 | |||||||
| chr2:230287152 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(83): Show |
92 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1646-740T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287152 | |||||||
| chr2:230287238 | T | C | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1646-654T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287238 | |||||||
| chr2:230287256 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1646-636G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287256 | |||||||
| chr2:230287411 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1646-481G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287411 | |||||||
| chr2:230287475 | C | A | 1 | a0001c0001t0002g0051 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1646-417C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287475 | |||||||
| chr2:230287484 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1646-408C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287484 | |||||||
| chr2:230287555 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1646-337A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287555 | |||||||
| chr2:230287584 | T | G | 1 | a0011c0014t0001g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1646-308T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287584 | |||||||
| chr2:230287984 | A | G | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1720+18A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230287984 | |||||||
| chr2:230288021 | C | T | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1720+55C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288021 | |||||||
| chr2:230288181 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1720+215G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288181 | |||||||
| chr2:230288247 | A | G | 11 | a0001c0001t0001g0152 a0001c0001t0001g0265 a0001c0001t0001g0269 others(8): Show |
11 | HG00323.hp2 HG00639.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1720+281A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288247 | |||||||
| chr2:230288268 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+302T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288268 | |||||||
| chr2:230288345 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1720+379G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288345 | |||||||
| chr2:230288455 | A | ATCTT | 31 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0052 others(28): Show |
33 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1720+555_1720+558d others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | ||||||
| chr2:230288455 | A | ATCTTTCT others(1): Show |
15 | a0001c0001t0001g0050 a0001c0001t0001g0073 a0001c0001t0001g0075 others(12): Show |
15 | HG01123.hp1 HG01433.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.1720+551_1720+558d others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | ||||||
| chr2:230288455 | A | ATCTTTCT others(5): Show |
5 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0182 others(2): Show |
5 | HG00323.hp1 HG02055.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+547_1720+558d others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | ||||||
| chr2:230288455 | A | ATCTTTCT others(13): Show |
2 | a0004c0003t0001g0300 a0004c0003t0001g0311 |
2 | HG01884.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1720+539_1720+558d others(22): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | ||||||
| chr2:230288455 | A | T | 1 | a0002c0002t0001g0331 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1720+489A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288455 | |||||||
| chr2:230288455 | ATCTT | A | 46 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0016 others(43): Show |
49 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1720+555_1720+558d others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | ||||||
| chr2:230288455 | ATCTTTCT others(1): Show |
A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0054 others(19): Show |
25 | HG00140.hp2 HG00735.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1720+551_1720+558d others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | ||||||
| chr2:230288455 | ATCTTTCT others(5): Show |
A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0071 a0001c0001t0001g0096 others(10): Show |
14 | HG00741.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1720+547_1720+558d others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | ||||||
| chr2:230288455 | ATCTTTCT others(9): Show |
A | 7 | a0001c0001t0001g0090 a0003c0004t0003g0030 a0003c0004t0003g0031 others(4): Show |
7 | HG00280.hp1 HG00738.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1720+543_1720+558d others(18): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | ||||||
| chr2:230288455 | ATCTTTCT others(13): Show |
A | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1720+539_1720+558d others(22): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | ||||||
| chr2:230288455 | ATCTTTCT others(17): Show |
A | 1 | a0001c0001t0001g0023 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1720+535_1720+558d others(26): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | ||||||
| chr2:230288489 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1720+523C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288489 | |||||||
| chr2:230288503 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1720+537T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288503 | |||||||
| chr2:230288505 | CTTTCTTT others(6): Show |
C | 1 | a0001c0001t0001g0278 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1720+542_1720+554d others(15): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288505 | ||||||
| chr2:230288505 | CTTTCTTT others(13): Show |
C | 1 | a0001c0001t0001g0150 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1720+543_1720+562d others(22): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288505 | ||||||
| chr2:230288509 | C | CTTTCTTT others(9): Show |
2 | a0001c0001t0001g0156 a0009c0013t0001g0143 |
2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1720+547_1720+562d others(18): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288509 | ||||||
| chr2:230288509 | C | CTTTCTTT others(5): Show |
2 | a0001c0001t0001g0211 a0009c0013t0001g0144 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1720+554_1720+555i others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288509 | ||||||
| chr2:230288509 | CTTTCTTT others(2): Show |
C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0283 a0001c0001t0001g0310 |
3 | HG02572.hp1 HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1720+546_1720+554d others(11): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288509 | ||||||
| chr2:230288513 | CTTTCT | C | 14 | a0001c0001t0001g0020 a0001c0001t0001g0284 a0001c0001t0001g0293 others(11): Show |
14 | HG01261.hp2 HG01516.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1720+550_1720+554d others(7): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288513 | ||||||
| chr2:230288513 | CTTTCTTT others(5): Show |
C | 1 | a0001c0001t0001g0145 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1720+551_1720+562d others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288513 | ||||||
| chr2:230288517 | CT | C | 28 | a0001c0001t0001g0020 a0001c0001t0001g0200 a0001c0001t0001g0226 others(25): Show |
30 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.1720+554delT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288517 | ||||||
| chr2:230288518 | T | TTTC | 37 | a0001c0001t0001g0018 a0001c0001t0001g0185 a0001c0001t0001g0195 others(34): Show |
37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1720+555_1720+557d others(5): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288518 | ||||||
| chr2:230288518 | T | TTTCTTTC | 25 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0094 others(22): Show |
26 | HG00639.hp1 HG01081.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.1720+558_1720+559i others(9): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288518 | ||||||
| chr2:230288518 | T | TTTCTTTC others(4): Show |
14 | a0001c0001t0001g0241 a0001c0001t0001g0290 a0001c0001t0001g0291 others(11): Show |
14 | HG01069.hp2 HG01081.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1720+558_1720+559i others(13): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288518 | ||||||
| chr2:230288518 | T | TTTCTTTC others(12): Show |
3 | a0001c0001t0001g0206 a0001c0001t0001g0289 a0002c0002t0001g0333 |
3 | HG01099.hp1 HG01346.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1720+558_1720+559i others(21): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288518 | ||||||
| chr2:230288521 | CT | C | 5 | a0001c0001t0001g0026 a0001c0001t0001g0135 a0001c0001t0001g0198 others(2): Show |
5 | HG00673.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+562delT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288521 | ||||||
| chr2:230288522 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1720+556T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288522 | |||||||
| chr2:230288522 | T | TTTC | 4 | a0001c0001t0001g0132 a0001c0001t0001g0216 a0001c0006t0001g0035 others(1): Show |
4 | HG00140.hp1 NA18949.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+558_1720+559i others(5): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288522 | ||||||
| chr2:230288522 | T | TTTCTTTC others(4): Show |
1 | a0001c0001t0001g0162 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1720+558_1720+559i others(13): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288522 | ||||||
| chr2:230288522 | T | TTTCTTTC others(7): Show |
1 | a0001c0001t0002g0271 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1720+558_1720+559i others(16): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288522 | ||||||
| chr2:230288523 | T | TTCTTTCT others(3): Show |
1 | a0001c0001t0001g0136 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1720+558_1720+559i others(12): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288523 | ||||||
| chr2:230288524 | T | TC | 4 | a0001c0001t0001g0063 a0001c0001t0001g0078 a0001c0001t0001g0255 others(1): Show |
4 | HG00621.hp2 HG01071.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+558_1720+559i others(3): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288524 | |||||||
| chr2:230288539 | T | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(74): Show |
83 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1720+573T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288539 | |||||||
| chr2:230288645 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0123 |
2 | HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1720+679G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288645 | |||||||
| chr2:230288671 | C | T | 2 | a0009c0013t0001g0143 a0009c0013t0001g0144 |
2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1720+705C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288671 | |||||||
| chr2:230288713 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1720+747T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288713 | |||||||
| chr2:230288773 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0098 |
2 | HG00741.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1720+807T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288773 | |||||||
| chr2:230289137 | C | T | 1 | a0002c0002t0001g0327 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1720+1171C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230289137 | |||||||
| chr2:230289169 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+1203G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230289169 | |||||||
| chr2:230289297 | A | G | 25 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(22): Show |
27 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.1721-1163A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230289297 | |||||||
| chr2:230289375 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1721-1085A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230289375 | |||||||
| chr2:230289694 | C | T | 1 | a0001c0001t0002g0257 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1721-766C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230289694 | |||||||
| chr2:230289986 | A | C | 1 | a0002c0002t0001g0339 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1721-474A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230289986 | |||||||
| chr2:230290412 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1721-48G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230290412 | |||||||
| chr2:230290415 | G | A | 3 | a0001c0001t0002g0251 a0001c0001t0002g0253 a0001c0001t0002g0258 |
3 | HG02258.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1721-45G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230290415 | |||||||
| chr2:230290698 | T | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(65): Show |
74 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1825+134T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230290698 | |||||||
| chr2:230290823 | G | A | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1825+259G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230290823 | |||||||
| chr2:230290989 | T | C | 143 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(140): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1825+425T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230290989 | |||||||
| chr2:230291275 | T | C | 1 | a0004c0003t0001g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1825+711T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230291275 | |||||||
| chr2:230291365 | C | G | 1 | a0003c0004t0003g0006 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1825+801C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230291365 | |||||||
| chr2:230291457 | C | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0156 a0001c0001t0001g0210 others(8): Show |
12 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1825+893C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230291457 | |||||||
| chr2:230291719 | T | C | 2 | a0001c0001t0004g0250 a0001c0001t0004g0312 |
2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-927T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230291719 | |||||||
| chr2:230291769 | G | T | 16 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(13): Show |
18 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1826-877G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230291769 | |||||||
| chr2:230291959 | C | T | 7 | a0001c0001t0001g0156 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-687C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230291959 | |||||||
| chr2:230292063 | T | C | 4 | a0004c0003t0001g0261 a0004c0003t0001g0262 a0004c0003t0001g0263 others(1): Show |
4 | HG01884.hp1 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-583T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230292063 | |||||||
| chr2:230292225 | T | A | 3 | a0003c0004t0003g0030 a0003c0004t0003g0031 a0003c0004t0003g0032 |
3 | HG00738.hp2 HG01496.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1826-421T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230292225 | |||||||
| chr2:230292238 | C | T | 1 | a0001c0011t0001g0202 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1826-408C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230292238 | |||||||
| chr2:230292452 | C | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1826-194C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230292452 | |||||||
| chr2:230292556 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(73): Show |
82 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1826-90T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230292556 | |||||||
| chr2:230292599 | C | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0120 a0001c0001t0001g0216 |
3 | NA18949.hp1 NA18974.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1826-47C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230292599 | |||||||
| chr2:230292797 | A | G | 25 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(22): Show |
27 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.1968+9A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230292797 | |||||||
| chr2:230292812 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(247): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1968+24G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230292812 | |||||||
| chr2:230292835 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1968+47A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230292835 | |||||||
| chr2:230292853 | T | A | 1 | a0001c0001t0001g0293 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1968+65T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230292853 | |||||||
| chr2:230293021 | G | T | 1 | a0002c0002t0001g0332 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1968+233G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293021 | |||||||
| chr2:230293198 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1968+410C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293198 | |||||||
| chr2:230293283 | A | G | 2 | a0002c0002t0001g0318 a0002c0002t0001g0319 |
2 | HG01516.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1968+495A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293283 | |||||||
| chr2:230293395 | G | A | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1968+607G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293395 | |||||||
| chr2:230293509 | G | T | 1 | a0001c0011t0001g0202 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1968+721G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293509 | |||||||
| chr2:230293524 | A | G | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | HG01081.hp2 HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1968+736A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293524 | |||||||
| chr2:230293575 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-696G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293575 | |||||||
| chr2:230293607 | G | A | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0004c0003t0001g0229 |
3 | HG03098.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1969-664G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293607 | |||||||
| chr2:230293628 | G | A | 1 | a0012c0018t0001g0249 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1969-643G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293628 | |||||||
| chr2:230293926 | G | T | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1969-345G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293926 | |||||||
| chr2:230293935 | G | C | 1 | a0011c0014t0001g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1969-336G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293935 | |||||||
| chr2:230293995 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1969-276A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293995 | |||||||
| chr2:230294192 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1969-79T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230294192 | |||||||
| chr2:230294216 | A | T | 7 | a0001c0001t0001g0156 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1969-55A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230294216 | |||||||
| chr2:230294227 | G | A | 4 | a0002c0002t0001g0153 a0002c0002t0001g0314 a0002c0002t0001g0316 others(1): Show |
4 | HG00408.hp2 HG01934.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1969-44G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230294227 | |||||||
| chr2:230294320 | T | G | 1 | a0001c0001t0001g0224 | 1 | NA19067.hp1 | splice_donor_variant&intron_variant | HIGH | c.2016+2T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294320 | |||||||
| chr2:230294321 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA19067.hp1 | splice_region_variant&intron_variant | LOW | c.2016+3G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294321 | |||||||
| chr2:230294322 | A | T | 1 | a0001c0001t0001g0224 | 1 | NA19067.hp1 | splice_region_variant&intron_variant | LOW | c.2016+4A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294322 | |||||||
| chr2:230294415 | T | A | 1 | a0001c0001t0001g0095 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2016+97T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294415 | |||||||
| chr2:230294570 | C | A | 1 | a0004c0003t0001g0305 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2016+252C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294570 | |||||||
| chr2:230294573 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2016+255G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294573 | |||||||
| chr2:230294695 | T | A | 33 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(30): Show |
37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.2016+377T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294695 | |||||||
| chr2:230294773 | G | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(93): Show |
103 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.2016+455G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294773 | |||||||
| chr2:230295119 | T | G | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2016+801T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230295119 | |||||||
| chr2:230295391 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2016+1073A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230295391 | |||||||
| chr2:230295429 | A | G | 2 | a0001c0001t0002g0192 a0001c0001t0002g0194 |
2 | NA18953.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2016+1111A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230295429 | |||||||
| chr2:230295446 | G | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0293 |
2 | HG03017.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2016+1128G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230295446 | |||||||
| chr2:230295448 | T | G | 2 | a0004c0003t0001g0301 a0004c0003t0001g0311 |
2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2016+1130T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230295448 | |||||||
| chr2:230295596 | T | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0140 |
2 | NA18962.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.2016+1278T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230295596 | |||||||
| chr2:230295806 | A | G | 35 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(32): Show |
42 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.2016+1488A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230295806 | |||||||
| chr2:230296003 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2017-1418C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296003 | |||||||
| chr2:230296013 | A | C | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2017-1408A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296013 | |||||||
| chr2:230296076 | CA | C | 145 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(142): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.2017-1330delA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 230296076 | ||||||
| chr2:230296076 | CAA | C | 5 | a0001c0001t0002g0003 a0001c0001t0002g0251 a0001c0001t0002g0252 others(2): Show |
7 | HG02258.hp2 HG02717.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2017-1331_2017-133 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 230296076 | ||||||
| chr2:230296290 | A | G | 34 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2017-1131A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296290 | |||||||
| chr2:230296311 | T | C | 25 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(22): Show |
27 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.2017-1110T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296311 | |||||||
| chr2:230296474 | C | A | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2017-947C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296474 | |||||||
| chr2:230296619 | G | A | 2 | a0006c0009t0004g0158 a0006c0009t0004g0159 |
2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2017-802G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296619 | |||||||
| chr2:230296622 | T | A | 143 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(140): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.2017-799T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296622 | |||||||
| chr2:230296798 | G | A | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2017-623G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296798 | |||||||
| chr2:230296807 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2017-614A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296807 | |||||||
| chr2:230296830 | C | A | 10 | a0001c0001t0001g0068 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | NA18943.hp1 NA18949.hp1 NA18956.hp2 others(7): Show |
intron_variant | MODIFIER | c.2017-591C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296830 | |||||||
| chr2:230297128 | G | C | 9 | a0001c0001t0004g0250 a0001c0001t0004g0312 a0004c0003t0001g0302 others(6): Show |
9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2017-293G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230297128 | |||||||
| chr2:230297155 | A | C | 7 | a0001c0001t0001g0156 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2017-266A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230297155 | |||||||
| chr2:230297227 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2017-194A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230297227 | |||||||
| chr2:230297303 | T | G | 1 | a0001c0001t0001g0182 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2017-118T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230297303 | |||||||
| chr2:230297339 | G | T | 7 | a0001c0001t0001g0156 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2017-82G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230297339 | |||||||
| chr2:230297626 | G | T | 140 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(137): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.2058+164G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230297626 | |||||||
| chr2:230297685 | T | A | 1 | a0001c0001t0001g0135 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2058+223T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230297685 | |||||||
| chr2:230297898 | T | C | 3 | a0004c0003t0001g0302 a0004c0003t0001g0303 a0004c0003t0001g0304 |
3 | HG02615.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2058+436T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230297898 | |||||||
| chr2:230297974 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2058+512T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230297974 | |||||||
| chr2:230298040 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2058+578A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298040 | |||||||
| chr2:230298211 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2058+749A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298211 | |||||||
| chr2:230298240 | G | A | 117 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(114): Show |
130 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.2058+778G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298240 | |||||||
| chr2:230298283 | C | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(245): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.2058+821C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298283 | |||||||
| chr2:230298284 | G | A | 1 | a0005c0007t0001g0127 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2058+822G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298284 | |||||||
| chr2:230298383 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2058+921G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298383 | |||||||
| chr2:230298474 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2058+1012T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298474 | |||||||
| chr2:230298673 | G | C | 151 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(148): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.2058+1211G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298673 | |||||||
| chr2:230298762 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0280 others(2): Show |
6 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2058+1300G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298762 | |||||||
| chr2:230298904 | C | A | 2 | a0004c0003t0001g0301 a0004c0003t0001g0311 |
2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2058+1442C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298904 | |||||||
| chr2:230298930 | T | A | 1 | a0001c0001t0002g0258 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2058+1468T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298930 | |||||||
| chr2:230298955 | G | A | 10 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(7): Show |
10 | HG00323.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2058+1493G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298955 | |||||||
| chr2:230299050 | A | T | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0116 others(1): Show |
4 | HG00621.hp2 HG02074.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.2058+1588A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299050 | |||||||
| chr2:230299219 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2058+1757G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299219 | |||||||
| chr2:230299447 | G | A | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2058+1985G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299447 | |||||||
| chr2:230299469 | C | T | 1 | a0002c0002t0001g0316 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2058+2007C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299469 | |||||||
| chr2:230299484 | C | T | 3 | a0001c0001t0002g0251 a0001c0001t0002g0253 a0001c0001t0002g0258 |
3 | HG02258.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2058+2022C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299484 | |||||||
| chr2:230299560 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2058+2098G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299560 | |||||||
| chr2:230299833 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2058+2371C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299833 | |||||||
| chr2:230299862 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2058+2400C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299862 | |||||||
| chr2:230300067 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2058+2605A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230300067 | |||||||
| chr2:230300221 | C | T | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2058+2759C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230300221 | |||||||
| chr2:230300413 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2058+2951A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230300413 | |||||||
| chr2:230300651 | GCAGCTCT others(18): Show |
G | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2058+3190_2058+321 others(29): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230300651 | |||||||
| chr2:230300683 | G | A | 1 | a0003c0005t0003g0218 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2058+3221G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230300683 | |||||||
| chr2:230300836 | C | G | 7 | a0001c0001t0001g0156 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2058+3374C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230300836 | |||||||
| chr2:230301124 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2058+3662A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301124 | |||||||
| chr2:230301197 | C | G | 1 | a0001c0001t0002g0231 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2058+3735C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301197 | |||||||
| chr2:230301214 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2058+3752A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301214 | |||||||
| chr2:230301220 | G | A | 33 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0151 others(30): Show |
37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.2058+3758G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301220 | |||||||
| chr2:230301221 | C | T | 34 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(31): Show |
41 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.2058+3759C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301221 | |||||||
| chr2:230301392 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2058+3930G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301392 | |||||||
| chr2:230301402 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2058+3940A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301402 | |||||||
| chr2:230301653 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2058+4191A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301653 | |||||||
| chr2:230301656 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(248): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2058+4194T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301656 | |||||||
| chr2:230302125 | C | T | 139 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(136): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.2058+4663C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230302125 | |||||||
| chr2:230302229 | CA | C | 7 | a0001c0001t0001g0168 a0001c0001t0002g0243 a0001c0001t0004g0312 others(4): Show |
7 | HG01884.hp1 HG02572.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2058+4782delA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230302229 | ||||||
| chr2:230302574 | C | G | 2 | a0002c0002t0001g0318 a0002c0002t0001g0319 |
2 | HG01516.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2058+5112C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230302574 | |||||||
| chr2:230302641 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2058+5179A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230302641 | |||||||
| chr2:230302863 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2058+5401G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230302863 | |||||||
| chr2:230303094 | A | T | 1 | a0004c0003t0001g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2058+5632A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303094 | |||||||
| chr2:230303219 | G | A | 2 | a0002c0002t0001g0153 a0002c0002t0001g0320 |
2 | HG01934.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.2058+5757G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303219 | |||||||
| chr2:230303239 | C | T | 1 | a0002c0002t0001g0330 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2058+5777C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303239 | |||||||
| chr2:230303242 | C | T | 7 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2058+5780C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303242 | |||||||
| chr2:230303262 | T | G | 2 | a0001c0001t0002g0234 a0001c0001t0002g0237 |
2 | HG01069.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2058+5800T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303262 | |||||||
| chr2:230303419 | A | C | 1 | a0002c0002t0001g0153 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2058+5957A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303419 | |||||||
| chr2:230303534 | A | G | 2 | a0001c0001t0001g0341 a0004c0003t0001g0229 |
2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2058+6072A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303534 | |||||||
| chr2:230303807 | A | T | 1 | a0001c0001t0001g0209 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2059-6117A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303807 | |||||||
| chr2:230303977 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
6 | HG01106.hp2 HG02015.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2059-5947G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303977 | |||||||
| chr2:230304050 | G | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(74): Show |
83 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.2059-5874G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230304050 | |||||||
| chr2:230304185 | G | A | 137 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(134): Show |
150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.2059-5739G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230304185 | |||||||
| chr2:230304287 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG01106.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2059-5637G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230304287 | |||||||
| chr2:230304469 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2059-5455A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230304469 | |||||||
| chr2:230305009 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(83): Show |
92 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2059-4915G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305009 | |||||||
| chr2:230305046 | A | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0163 a0001c0001t0001g0165 |
3 | NA18980.hp1 NA18998.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2059-4878A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305046 | |||||||
| chr2:230305146 | T | G | 1 | a0001c0001t0001g0180 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2059-4778T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305146 | |||||||
| chr2:230305196 | G | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2059-4728G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305196 | |||||||
| chr2:230305459 | T | A | 1 | a0001c0001t0001g0287 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2059-4465T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305459 | |||||||
| chr2:230305548 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2059-4376G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305548 | |||||||
| chr2:230305554 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(73): Show |
82 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.2059-4370A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305554 | |||||||
| chr2:230305664 | C | A | 35 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(32): Show |
42 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.2059-4260C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305664 | |||||||
| chr2:230305674 | G | A | 1 | a0003c0004t0003g0028 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2059-4250G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305674 | |||||||
| chr2:230305685 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2059-4239C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305685 | |||||||
| chr2:230305686 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2059-4238G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305686 | |||||||
| chr2:230305700 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2059-4224A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305700 | |||||||
| chr2:230305761 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2059-4163C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305761 | |||||||
| chr2:230305789 | G | A | 34 | a0001c0001t0001g0088 a0002c0002t0001g0004 a0002c0002t0001g0021 others(31): Show |
38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2059-4135G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305789 | |||||||
| chr2:230305800 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0002g0235 a0001c0001t0002g0245 |
4 | NA18956.hp1 NA18960.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.2059-4124G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305800 | |||||||
| chr2:230305916 | C | T | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2059-4008C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305916 | |||||||
| chr2:230306479 | C | T | 22 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(19): Show |
24 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2059-3445C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230306479 | |||||||
| chr2:230306515 | G | T | 2 | a0002c0002t0001g0326 a0002c0008t0001g0317 |
2 | HG01070.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2059-3409G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230306515 | |||||||
| chr2:230306638 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-3286A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230306638 | |||||||
| chr2:230306708 | C | T | 22 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(19): Show |
24 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2059-3216C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230306708 | |||||||
| chr2:230306806 | G | T | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-3118G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230306806 | |||||||
| chr2:230306848 | C | A | 2 | a0001c0001t0001g0285 a0001c0001t0001g0306 |
2 | HG00099.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.2059-3076C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230306848 | |||||||
| chr2:230307174 | A | G | 10 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(7): Show |
10 | HG00323.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2059-2750A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307174 | |||||||
| chr2:230307195 | C | T | 1 | a0002c0002t0001g0320 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2059-2729C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307195 | |||||||
| chr2:230307260 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2059-2664G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307260 | |||||||
| chr2:230307286 | G | A | 2 | a0007c0012t0001g0024 a0007c0012t0001g0025 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2059-2638G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307286 | |||||||
| chr2:230307456 | T | A | 1 | a0001c0001t0001g0266 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2059-2468T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307456 | |||||||
| chr2:230307589 | T | G | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-2335T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307589 | |||||||
| chr2:230307824 | A | G | 47 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0094 others(44): Show |
49 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.2059-2100A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307824 | |||||||
| chr2:230307826 | T | C | 1 | a0001c0001t0002g0256 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2059-2098T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307826 | |||||||
| chr2:230307890 | G | A | 1 | a0002c0002t0001g0322 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2059-2034G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307890 | |||||||
| chr2:230307927 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(234): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.2059-1997T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307927 | |||||||
| chr2:230307955 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-1969G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307955 | |||||||
| chr2:230307955 | G | GTA | 20 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0084 others(17): Show |
23 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.2059-1934_2059-193 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | ||||||
| chr2:230307955 | G | GTATA | 15 | a0001c0001t0001g0139 a0001c0001t0001g0206 a0001c0001t0001g0287 others(12): Show |
18 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.2059-1936_2059-193 others(8): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | ||||||
| chr2:230307955 | G | GTATATA | 7 | a0001c0001t0001g0020 a0001c0001t0001g0106 a0001c0001t0001g0289 others(4): Show |
8 | HG00558.hp2 HG01346.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.2059-1938_2059-193 others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | ||||||
| chr2:230307955 | G | GTATATAT others(1): Show |
7 | a0001c0001t0001g0048 a0001c0001t0001g0266 a0001c0001t0001g0282 others(4): Show |
7 | HG00735.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2059-1940_2059-193 others(12): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | ||||||
| chr2:230307955 | G | GTATATAT others(3): Show |
13 | a0001c0001t0001g0094 a0001c0001t0001g0189 a0001c0001t0001g0190 others(10): Show |
13 | HG00735.hp2 HG01109.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.2059-1942_2059-193 others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | ||||||
| chr2:230307955 | G | GTATATAT others(5): Show |
9 | a0001c0001t0001g0019 a0001c0001t0001g0201 a0001c0001t0001g0204 others(6): Show |
10 | HG02074.hp2 HG03490.hp1 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.2059-1944_2059-193 others(16): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | ||||||
| chr2:230307955 | G | GTATATAT others(7): Show |
2 | a0001c0001t0001g0079 a0002c0002t0001g0327 |
2 | HG02523.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.2059-1946_2059-193 others(18): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | ||||||
| chr2:230307955 | G | GTATATAT others(9): Show |
7 | a0001c0001t0001g0185 a0001c0001t0001g0278 a0001c0001t0001g0283 others(4): Show |
7 | HG00099.hp1 HG01123.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.2059-1948_2059-193 others(20): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | ||||||
| chr2:230307955 | G | GTATATAT others(17): Show |
1 | a0001c0001t0001g0191 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2059-1956_2059-193 others(28): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | ||||||
| chr2:230307955 | GTA | G | 12 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0080 others(9): Show |
12 | HG02109.hp1 HG02486.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.2059-1934_2059-193 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | ||||||
| chr2:230307955 | GTATA | G | 8 | a0001c0001t0001g0092 a0001c0001t0001g0101 a0001c0001t0001g0113 others(5): Show |
8 | HG01109.hp1 HG02040.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.2059-1936_2059-193 others(8): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | ||||||
| chr2:230307955 | GTATATA | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(8): Show |
12 | HG00639.hp1 HG01074.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.2059-1938_2059-193 others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | ||||||
| chr2:230307955 | GTATATAT others(3): Show |
G | 3 | a0001c0001t0001g0023 a0001c0001t0002g0257 a0004c0003t0001g0229 |
4 | HG02896.hp1 HG02897.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.2059-1942_2059-193 others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | ||||||
| chr2:230307957 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2059-1967A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307957 | |||||||
| chr2:230307978 | TATATATA others(7): Show |
T | 3 | a0001c0001t0001g0178 a0001c0001t0001g0341 a0011c0014t0001g0259 |
3 | HG02486.hp1 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2059-1944_2059-193 others(18): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307978 | ||||||
| chr2:230307978 | TATATATA others(15): Show |
T | 2 | a0004c0003t0001g0301 a0004c0003t0001g0311 |
2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2059-1944_2059-192 others(26): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307978 | ||||||
| chr2:230307980 | TATATATA others(5): Show |
T | 2 | a0001c0001t0002g0234 a0001c0001t0002g0237 |
2 | HG01069.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2059-1942_2059-193 others(16): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307980 | ||||||
| chr2:230307980 | TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2059-1942_2059-192 others(18): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307980 | ||||||
| chr2:230307980 | TATATATA others(9): Show |
T | 4 | a0002c0002t0001g0153 a0002c0002t0001g0314 a0002c0002t0001g0316 others(1): Show |
4 | HG00408.hp2 HG01934.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2059-1942_2059-192 others(20): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307980 | ||||||
| chr2:230307980 | TATATATA others(13): Show |
T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG02723.hp2 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2059-1942_2059-192 others(24): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307980 | ||||||
| chr2:230307982 | TATATATA others(3): Show |
T | 25 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(22): Show |
30 | HG00423.hp1 HG02109.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.2059-1940_2059-193 others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307982 | ||||||
| chr2:230307982 | TATATATA others(11): Show |
T | 2 | a0009c0013t0001g0143 a0009c0013t0001g0144 |
2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2059-1940_2059-192 others(22): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307982 | ||||||
| chr2:230307984 | TATATATA others(1): Show |
T | 4 | a0001c0001t0001g0011 a0001c0001t0002g0003 a0001c0001t0002g0240 others(1): Show |
5 | HG02056.hp2 HG02683.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2059-1938_2059-193 others(12): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307984 | ||||||
| chr2:230307984 | TATATATA others(3): Show |
T | 3 | a0001c0001t0002g0208 a0001c0001t0002g0236 a0001c0001t0002g0247 |
3 | HG00642.hp1 HG01255.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2059-1938_2059-192 others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307984 | ||||||
| chr2:230307986 | T | C | 1 | a0001c0001t0001g0342 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2059-1938T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307986 | |||||||
| chr2:230307986 | TATATAC | T | 22 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0001g0130 others(19): Show |
23 | HG00423.hp2 HG00621.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.2059-1936_2059-193 others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307986 | ||||||
| chr2:230307986 | TATATACA others(1): Show |
T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0177 others(6): Show |
10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2059-1936_2059-192 others(12): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307986 | ||||||
| chr2:230307988 | T | C | 1 | a0001c0001t0001g0342 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2059-1936T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307988 | |||||||
| chr2:230307988 | TATAC | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0049 others(18): Show |
23 | HG00558.hp1 HG00741.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.2059-1934_2059-193 others(8): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307988 | ||||||
| chr2:230307988 | TATACAC | T | 6 | a0001c0001t0001g0073 a0001c0001t0001g0174 a0004c0003t0001g0261 others(3): Show |
6 | HG00099.hp2 HG01884.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2059-1934_2059-192 others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307988 | ||||||
| chr2:230307989 | A | C | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-1935A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307989 | |||||||
| chr2:230307990 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0026 others(13): Show |
18 | HG01106.hp2 HG01109.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2059-1934T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307990 | |||||||
| chr2:230307990 | T | TAC | 3 | a0001c0001t0001g0152 a0001c0001t0001g0270 a0007c0017t0001g0061 |
3 | HG00323.hp2 HG00639.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2059-1908_2059-190 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | T | TATATATA others(5): Show |
1 | a0003c0005t0003g0104 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2059-1933_2059-193 others(16): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | T | TATATATA others(5): Show |
5 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0006t0001g0045 others(2): Show |
5 | HG01256.hp1 HG02148.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(16): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | T | TATATATA others(7): Show |
3 | a0001c0001t0001g0293 a0003c0005t0003g0187 a0003c0005t0003g0188 |
3 | HG01069.hp1 HG01071.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(18): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | T | TATATATA others(9): Show |
1 | a0001c0001t0007g0184 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2059-1933_2059-193 others(20): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | T | TATATATA others(9): Show |
2 | a0001c0001t0001g0196 a0003c0004t0003g0006 |
3 | HG01106.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(20): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | T | TATATATA others(11): Show |
5 | a0001c0006t0001g0037 a0003c0004t0003g0008 a0003c0004t0003g0038 others(2): Show |
5 | HG01243.hp1 HG01255.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(22): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | T | TATATATA others(13): Show |
3 | a0001c0006t0001g0035 a0003c0004t0003g0008 a0003c0004t0003g0040 |
3 | HG00140.hp1 HG01169.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(24): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | T | TATATATA others(15): Show |
1 | a0004c0003t0001g0305 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2059-1933_2059-193 others(26): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | T | TATATATA others(15): Show |
3 | a0001c0006t0002g0029 a0003c0005t0003g0105 a0003c0005t0003g0166 |
3 | HG00140.hp2 HG00323.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(26): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | T | TATATATA others(21): Show |
1 | a0003c0004t0003g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2059-1933_2059-193 others(32): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | T | TATATATA others(17): Show |
3 | a0001c0006t0001g0036 a0001c0006t0001g0039 a0003c0004t0003g0030 |
3 | HG01358.hp2 HG02258.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(28): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | T | TATATATA others(19): Show |
2 | a0003c0004t0003g0031 a0003c0004t0010g0033 |
2 | HG00738.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(30): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | T | TATATATA others(21): Show |
3 | a0001c0001t0001g0277 a0003c0004t0003g0043 a0003c0005t0003g0203 |
3 | HG02738.hp2 HG03704.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(32): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | TAC | T | 38 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0064 others(35): Show |
39 | HG00597.hp1 HG00597.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.2059-1908_2059-190 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307990 | TACAC | T | 3 | a0001c0001t0001g0149 a0002c0002t0001g0323 a0002c0002t0001g0339 |
3 | HG02155.hp1 HG04115.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.2059-1910_2059-190 others(8): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | ||||||
| chr2:230307992 | C | T | 77 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0084 others(74): Show |
83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.2059-1932C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307992 | |||||||
| chr2:230307994 | C | T | 27 | a0001c0001t0004g0250 a0001c0001t0004g0312 a0001c0001t0005g0126 others(24): Show |
30 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.2059-1930C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307994 | |||||||
| chr2:230307996 | C | T | 24 | a0001c0001t0005g0126 a0002c0002t0001g0004 a0002c0002t0001g0151 others(21): Show |
27 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.2059-1928C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307996 | |||||||
| chr2:230307998 | C | T | 2 | a0001c0001t0005g0126 a0002c0002t0001g0326 |
2 | HG01070.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2059-1926C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307998 | |||||||
| chr2:230308000 | C | T | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2059-1924C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308000 | |||||||
| chr2:230308002 | C | T | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2059-1922C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308002 | |||||||
| chr2:230308004 | C | T | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2059-1920C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308004 | |||||||
| chr2:230308006 | C | T | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2059-1918C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308006 | |||||||
| chr2:230308016 | C | G | 36 | a0001c0001t0001g0018 a0001c0001t0001g0241 a0001c0001t0001g0246 others(33): Show |
43 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.2059-1908C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308016 | |||||||
| chr2:230308018 | G | C | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2059-1906G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308018 | |||||||
| chr2:230308020 | GAC | G | 7 | a0001c0001t0001g0156 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2059-1887_2059-188 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230308020 | ||||||
| chr2:230308070 | G | C | 2 | a0001c0001t0001g0284 a0001c0001t0001g0307 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2059-1854G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308070 | |||||||
| chr2:230308155 | G | A | 1 | a0004c0003t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2059-1769G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308155 | |||||||
| chr2:230308218 | T | A | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-1706T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308218 | |||||||
| chr2:230308282 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0341 a0001c0001t0001g0342 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2059-1642A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308282 | |||||||
| chr2:230308308 | T | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0134 |
3 | NA19063.hp2 NA19082.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2059-1616T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308308 | |||||||
| chr2:230308493 | G | A | 2 | a0001c0001t0001g0284 a0001c0001t0001g0307 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2059-1431G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308493 | |||||||
| chr2:230308542 | G | A | 5 | a0001c0001t0001g0156 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
5 | HG01884.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2059-1382G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308542 | |||||||
| chr2:230308571 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0154 a0001c0001t0001g0176 others(1): Show |
6 | HG01123.hp2 HG01981.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.2059-1353G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308571 | |||||||
| chr2:230308592 | G | A | 7 | a0001c0001t0001g0156 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2059-1332G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308592 | |||||||
| chr2:230308605 | G | T | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-1319G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308605 | |||||||
| chr2:230308773 | T | A | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-1151T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308773 | |||||||
| chr2:230308774 | A | C | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-1150A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308774 | |||||||
| chr2:230308775 | C | A | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-1149C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308775 | |||||||
| chr2:230308775 | C | T | 13 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0123 others(10): Show |
13 | HG01099.hp2 HG01123.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2059-1149C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308775 | |||||||
| chr2:230308782 | C | G | 5 | a0003c0004t0003g0041 a0003c0004t0003g0042 a0003c0004t0003g0043 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.2059-1142C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308782 | |||||||
| chr2:230308792 | G | A | 2 | a0004c0003t0001g0267 a0011c0014t0001g0259 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2059-1132G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308792 | |||||||
| chr2:230308825 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2059-1099C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308825 | |||||||
| chr2:230308926 | T | C | 1 | a0001c0001t0001g0342 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2059-998T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308926 | |||||||
| chr2:230308963 | A | T | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-961A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308963 | |||||||
| chr2:230309139 | G | A | 1 | a0002c0002t0001g0339 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2059-785G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309139 | |||||||
| chr2:230309202 | T | A | 1 | a0001c0001t0001g0206 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2059-722T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309202 | |||||||
| chr2:230309239 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(4): Show |
8 | HG01106.hp2 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2059-685C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309239 | |||||||
| chr2:230309263 | G | C | 2 | a0001c0001t0001g0181 a0001c0016t0001g0275 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2059-661G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309263 | |||||||
| chr2:230309322 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2059-602C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309322 | |||||||
| chr2:230309374 | A | C | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-550A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309374 | |||||||
| chr2:230309382 | T | C | 94 | a0001c0001t0001g0020 a0001c0001t0001g0152 a0001c0001t0001g0156 others(91): Show |
104 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.2059-542T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309382 | |||||||
| chr2:230309386 | C | G | 33 | a0001c0011t0001g0169 a0001c0011t0001g0202 a0002c0002t0001g0004 others(30): Show |
36 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.2059-538C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309386 | |||||||
| chr2:230309423 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2059-501G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309423 | |||||||
| chr2:230309423 | G | C | 94 | a0001c0001t0001g0020 a0001c0001t0001g0152 a0001c0001t0001g0156 others(91): Show |
104 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.2059-501G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309423 | |||||||
| chr2:230309590 | C | T | 94 | a0001c0001t0001g0020 a0001c0001t0001g0152 a0001c0001t0001g0156 others(91): Show |
104 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.2059-334C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309590 | |||||||
| chr2:230309688 | T | C | 1 | a0002c0002t0001g0313 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2059-236T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309688 | |||||||
| chr2:230309705 | G | A | 113 | a0001c0001t0001g0020 a0001c0001t0001g0152 a0001c0001t0001g0156 others(110): Show |
126 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.2059-219G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309705 | |||||||
| chr2:230309708 | T | G | 1 | a0003c0004t0003g0028 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2059-216T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309708 | |||||||
| chr2:230309847 | G | A | 1 | a0001c0001t0002g0251 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2059-77G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309847 | |||||||
| chr2:230309861 | C | G | 2 | a0001c0001t0001g0071 a0010c0020t0001g0137 |
2 | HG01192.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2059-63C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309861 | |||||||
| chr2:230310057 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2174+18G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310057 | |||||||
| chr2:230310273 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2174+234C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310273 | |||||||
| chr2:230310283 | C | T | 5 | a0001c0001t0004g0250 a0001c0001t0004g0312 a0006c0009t0004g0158 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2174+244C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310283 | |||||||
| chr2:230310375 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2174+336A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310375 | |||||||
| chr2:230310469 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2175-274C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310469 | |||||||
| chr2:230310536 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2175-207G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310536 | |||||||
| chr2:230310537 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2175-206A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310537 | |||||||
| chr2:230310578 | A | G | 1 | a0001c0001t0002g0238 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2175-165A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310578 | |||||||
| chr2:230310637 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2175-106A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310637 | |||||||
| chr2:230310670 | A | T | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2175-73A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310670 | |||||||
| chr2:230310725 | C | A | 10 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(7): Show |
10 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2175-18C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310725 | |||||||
| chr2:230310921 | G | C | 2 | a0001c0001t0004g0250 a0001c0001t0004g0312 |
2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2283+70G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/26 | chr2 | 230310921 | |||||||
| chr2:230310956 | C | T | 1 | a0011c0014t0001g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2283+105C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/26 | chr2 | 230310956 | |||||||
| chr2:230311048 | G | A | 113 | a0001c0001t0001g0020 a0001c0001t0001g0152 a0001c0001t0001g0156 others(110): Show |
126 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.2284-106G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/26 | chr2 | 230311048 | |||||||
| chr2:230311069 | A | C | 1 | a0003c0004t0003g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2284-85A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/26 | chr2 | 230311069 | |||||||
| chr2:230311080 | T | C | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-74T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/26 | chr2 | 230311080 | |||||||
| chr2:230311081 | C | G | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-73C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/26 | chr2 | 230311081 | |||||||
| chr2:230311098 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2284-56C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/26 | chr2 | 230311098 | |||||||
| chr2:230311263 | C | A | 1 | a0001c0001t0001g0193 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2361+32C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 25/26 | chr2 | 230311263 | |||||||
| chr2:230311274 | T | A | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2361+43T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 25/26 | chr2 | 230311274 | |||||||
| chr2:230311325 | G | A | 12 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0195 others(9): Show |
12 | HG00280.hp2 HG01099.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.2361+94G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 25/26 | chr2 | 230311325 | |||||||
| chr2:230311344 | C | T | 1 | a0011c0014t0001g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2362-108C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 25/26 | chr2 | 230311344 | |||||||
| chr2:230311448 | C | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG01081.hp2 HG01433.hp1 |
splice_region_variant&intron_variant | LOW | c.2362-4C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 25/26 | chr2 | 230311448 | |||||||
| chr2:230311767 | G | T | 1 | a0001c0001t0005g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2505+172G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 26/26 | chr2 | 230311767 | |||||||
| chr2:230311865 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0207 |
2 | NA18961.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2505+270A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 26/26 | chr2 | 230311865 | |||||||
| chr2:230312297 | G | A | 3 | a0004c0003t0001g0261 a0004c0003t0001g0263 a0004c0003t0001g0264 |
3 | HG02622.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2506-289G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 26/26 | chr2 | 230312297 | |||||||
| chr2:230312485 | CTT | C | 19 | a0003c0004t0003g0006 a0003c0004t0003g0008 a0003c0004t0003g0028 others(16): Show |
22 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.2506-92_2506-91del others(2): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 230312485 |