Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51575 |
| ensemblid | ENSG00000089048.15 |
| hgncid | 15898 |
| symbol | ESF1 |
| name | ESF1 nucleolar pre-rRNA processing protein homolog |
| refseq_nuc | NM_001276380.2 |
| refseq_prot | NP_001263309.1 |
| ensembl_nuc | ENST00000617257.2 |
| ensembl_prot | ENSP00000480783.2 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 13714325 |
| end | 13784919 |
| strand | - |
| ver | v1.2 |
| region | chr20:13714325-13784919 |
| region5000 | chr20:13709325-13789919 |
| regionname0 | ESF1_chr20_13714325_13784919 |
| regionname5000 | ESF1_chr20_13709325_13789919 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 851 | 288 | 67 | 42 | 133 | 11 | 35 | 111 | ESF1_chr20_13709325_13789919 | ESF1 | MSSKQ others(846): Show |
chr20 | 13709325 | 13789919 |
| a0002 | 1/0 | 851 | 59 | 10 | 13 | 23 | 4 | 8 | 17 | ESF1_chr20_13709325_13789919 | ESF1 | MSSKQ others(846): Show |
chr20 | 13709325 | 13789919 |
| a0003 | 0/1 | 851 | 23 | 2 | 6 | 9 | 1 | 4 | 5 | ESF1_chr20_13709325_13789919 | ESF1 | MSSKQ others(846): Show |
chr20 | 13709325 | 13789919 |
| a0004 | 0/0 | 850 | 10 | 0 | 0 | 10 | 0 | 0 | 7 | ESF1_chr20_13709325_13789919 | ESF1 | MSSKQ others(845): Show |
chr20 | 13709325 | 13789919 |
| a0005 | 0/0 | 851 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ESF1_chr20_13709325_13789919 | ESF1 | MSSKQ others(846): Show |
chr20 | 13709325 | 13789919 |
| a0006 | 0/0 | 851 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | MSSKQ others(846): Show |
chr20 | 13709325 | 13789919 |
| a0007 | 0/0 | 851 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | MSSKQ others(846): Show |
chr20 | 13709325 | 13789919 |
| a0008 | 0/0 | 851 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | MSSKQ others(846): Show |
chr20 | 13709325 | 13789919 |
| a0009 | 0/0 | 851 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | MSSKQ others(846): Show |
chr20 | 13709325 | 13789919 |
| a0010 | 0/0 | 851 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | MSSKQ others(846): Show |
chr20 | 13709325 | 13789919 |
| a0011 | 0/0 | 851 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | MSSKQ others(846): Show |
chr20 | 13709325 | 13789919 |
| a0012 | 0/0 | 851 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | MSSKQ others(846): Show |
chr20 | 13709325 | 13789919 |
| a0013 | 0/0 | 851 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | MSSKQ others(846): Show |
chr20 | 13709325 | 13789919 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2553 | 188 | 57 | 20 | 79 | 6 | 26 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0001c0002 | 0/0 | 2553 | 79 | 7 | 21 | 37 | 5 | 9 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0001c0005 | 0/0 | 2553 | 14 | 0 | 1 | 13 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0001c0007 | 0/0 | 2553 | 3 | 3 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0001c0008 | 0/0 | 2553 | 2 | 0 | 0 | 2 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0001c0012 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0001c0019 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0002c0003 | 1/0 | 2553 | 57 | 10 | 13 | 21 | 4 | 8 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0002c0010 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0002c0017 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0003c0004 | 0/1 | 2553 | 23 | 2 | 6 | 9 | 1 | 4 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0004c0006 | 0/0 | 2550 | 10 | 0 | 0 | 10 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2545): Show |
chr20 | 13709325 | 13789919 | ||
| a0005c0009 | 0/0 | 2553 | 2 | 0 | 0 | 2 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0006c0021 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0007c0015 | 0/0 | 2553 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0008c0013 | 0/0 | 2553 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0009c0018 | 0/0 | 2553 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0010c0020 | 0/0 | 2553 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0011c0011 | 0/0 | 2553 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0012c0016 | 0/0 | 2553 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 | ||
| a0013c0014 | 0/0 | 2553 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | ATGTC others(2548): Show |
chr20 | 13709325 | 13789919 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3188 | 159 | 36 | 19 | 75 | 6 | 23 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0001c0001t0002 | 0/0 | 3188 | 13 | 12 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0001c0001t0004 | 0/0 | 3188 | 6 | 6 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0001c0001t0005 | 0/0 | 3188 | 4 | 0 | 0 | 3 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0001c0001t0006 | 0/0 | 3188 | 3 | 3 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0001c0001t0008 | 0/0 | 3188 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0001c0001t0009 | 0/0 | 3188 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0001c0001t0010 | 0/0 | 3188 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0001c0002t0001 | 0/0 | 3188 | 79 | 7 | 21 | 37 | 5 | 9 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0001c0005t0001 | 0/0 | 3188 | 14 | 0 | 1 | 13 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0001c0007t0002 | 0/0 | 3188 | 3 | 3 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0001c0008t0001 | 0/0 | 3188 | 2 | 0 | 0 | 2 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0001c0012t0001 | 0/0 | 3188 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0001c0019t0001 | 0/0 | 3188 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0002c0003t0001 | 0/0 | 3188 | 42 | 1 | 11 | 20 | 2 | 8 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0002c0003t0003 | 1/0 | 3188 | 14 | 9 | 2 | 1 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0002c0003t0007 | 0/0 | 3188 | 1 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0002c0010t0001 | 0/0 | 3188 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0002c0017t0001 | 0/0 | 3188 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0003c0004t0002 | 0/1 | 3188 | 23 | 2 | 6 | 9 | 1 | 4 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0004c0006t0001 | 0/0 | 3185 | 10 | 0 | 0 | 10 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3180): Show |
chr20 | 13709325 | 13789919 |
| a0005c0009t0001 | 0/0 | 3188 | 2 | 0 | 0 | 2 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0006c0021t0001 | 0/0 | 3188 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0007c0015t0001 | 0/0 | 3188 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0008c0013t0001 | 0/0 | 3188 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0009c0018t0003 | 0/0 | 3188 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0010c0020t0001 | 0/0 | 3188 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0011c0011t0002 | 0/0 | 3188 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0012c0016t0003 | 0/0 | 3188 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| a0013c0014t0001 | 0/0 | 3188 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | GGGTG others(3183): Show |
chr20 | 13709325 | 13789919 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0004g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0006g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0008g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0009g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0001t0010g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0005t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0005t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0005t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0005t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0005t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0005t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0005t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0005t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0005t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0005t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0005t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0005t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0007t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0007t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0008t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0008t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0012t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0001c0019t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0003g0351 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0003g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0003g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0003g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0003g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0003g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0003t0007g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0010t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0002c0017t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0343 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0003c0004t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0004c0006t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0004c0006t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0004c0006t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0004c0006t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0004c0006t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0004c0006t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0004c0006t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0004c0006t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0004c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0004c0006t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0005c0009t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0005c0009t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0006c0021t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0007c0015t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0008c0013t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0009c0018t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0010c0020t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0011c0011t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0012c0016t0003g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| a0013c0014t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00140 | hp2 | a0002 | c0003 | t0001 | g0142 | EUR | GBR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00280 | hp1 | a0002 | c0003 | t0003 | g0135 | EUR | FIN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0211 | EUR | FIN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | FIN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00323 | hp2 | a0002 | c0003 | t0001 | g0165 | EUR | FIN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00408 | hp2 | a0001 | c0005 | t0001 | g0253 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00423 | hp2 | a0003 | c0004 | t0002 | g0333 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00438 | hp1 | a0006 | c0021 | t0001 | g0226 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00544 | hp1 | a0002 | c0010 | t0001 | g0139 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00597 | hp2 | a0003 | c0004 | t0002 | g0338 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00621 | hp1 | a0004 | c0006 | t0001 | g0227 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00621 | hp2 | a0002 | c0003 | t0001 | g0162 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00639 | hp1 | a0007 | c0015 | t0001 | g0081 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0277 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00642 | hp2 | a0002 | c0003 | t0003 | g0357 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00673 | hp1 | a0002 | c0003 | t0001 | g0157 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00733 | hp1 | a0003 | c0004 | t0002 | g0287 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0196 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00735 | hp1 | a0003 | c0004 | t0002 | g0286 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00738 | hp2 | a0002 | c0003 | t0001 | g0153 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0280 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0279 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0273 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01099 | hp1 | a0002 | c0003 | t0001 | g0141 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01099 | hp2 | a0002 | c0003 | t0001 | g0360 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01109 | hp1 | a0002 | c0003 | t0003 | g0133 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01167 | hp1 | a0002 | c0003 | t0001 | g0245 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0275 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0248 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01175 | hp1 | a0002 | c0003 | t0001 | g0244 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0214 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0174 | AMR | PUR | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0289 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01256 | hp1 | a0002 | c0003 | t0001 | g0158 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0290 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0288 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01261 | hp1 | a0008 | c0013 | t0001 | g0037 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01358 | hp2 | a0002 | c0003 | t0001 | g0359 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01361 | hp2 | a0009 | c0018 | t0003 | g0138 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01433 | hp1 | a0003 | c0004 | t0002 | g0339 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0268 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0266 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01496 | hp2 | a0001 | c0005 | t0001 | g0257 | AMR | CLM | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01515 | hp2 | a0002 | c0003 | t0007 | g0164 | EUR | IBS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0190 | EUR | IBS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0189 | EUR | IBS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01928 | hp1 | a0003 | c0004 | t0002 | g0335 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01934 | hp2 | a0002 | c0003 | t0001 | g0168 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01943 | hp2 | a0003 | c0004 | t0002 | g0224 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01975 | hp1 | a0003 | c0004 | t0002 | g0341 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0267 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0013 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02027 | hp1 | a0003 | c0004 | t0002 | g0022 | EAS | KHV | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02040 | hp1 | a0001 | c0005 | t0001 | g0249 | EAS | KHV | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02040 | hp2 | a0003 | c0004 | t0002 | g0330 | EAS | KHV | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02055 | hp2 | a0003 | c0004 | t0002 | g0334 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | KHV | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | KHV | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02135 | hp1 | a0002 | c0003 | t0001 | g0161 | EAS | KHV | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02145 | hp2 | a0010 | c0020 | t0001 | g0131 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02155 | hp1 | a0001 | c0005 | t0001 | g0002 | EAS | CDX | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | CDX | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02165 | hp1 | a0004 | c0006 | t0001 | g0231 | EAS | CDX | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02165 | hp2 | a0002 | c0003 | t0001 | g0148 | EAS | CDX | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02257 | hp1 | a0002 | c0003 | t0003 | g0358 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02257 | hp2 | a0001 | c0007 | t0002 | g0238 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02273 | hp2 | a0002 | c0003 | t0001 | g0013 | AMR | PEL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02451 | hp2 | a0003 | c0004 | t0002 | g0342 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02523 | hp2 | a0004 | c0006 | t0001 | g0230 | EAS | KHV | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0345 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02602 | hp2 | a0002 | c0003 | t0001 | g0167 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02683 | hp1 | a0003 | c0004 | t0002 | g0337 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02683 | hp2 | a0001 | c0001 | t0009 | g0216 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0270 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02717 | hp2 | a0011 | c0011 | t0002 | g0241 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0276 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02735 | hp2 | a0002 | c0003 | t0001 | g0163 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0283 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0225 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ESN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02965 | hp1 | a0001 | c0007 | t0002 | g0017 | AFR | ESN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02970 | hp1 | a0002 | c0003 | t0003 | g0134 | AFR | ESN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02970 | hp2 | a0002 | c0003 | t0003 | g0350 | AFR | ESN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02976 | hp1 | a0002 | c0003 | t0003 | g0352 | AFR | ESN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03017 | hp1 | a0002 | c0003 | t0001 | g0247 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03098 | hp1 | a0002 | c0003 | t0003 | g0137 | AFR | MSL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0171 | AFR | MSL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | ESN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | ESN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03209 | hp1 | a0001 | c0007 | t0002 | g0017 | AFR | MSL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03225 | hp1 | a0002 | c0003 | t0003 | g0349 | AFR | MSL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | MSL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0197 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03453 | hp1 | a0002 | c0003 | t0003 | g0354 | AFR | MSL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | MSL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03486 | hp2 | a0012 | c0016 | t0003 | g0356 | AFR | MSL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03490 | hp1 | a0002 | c0003 | t0001 | g0246 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03491 | hp1 | a0002 | c0003 | t0001 | g0151 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0152 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | GWD | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | MSL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03654 | hp1 | a0003 | c0004 | t0002 | g0340 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03669 | hp2 | a0013 | c0014 | t0001 | g0364 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | STU | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0122 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0269 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03710 | hp2 | a0002 | c0003 | t0001 | g0166 | SAS | PJL | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | BEB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03831 | hp2 | a0003 | c0004 | t0002 | g0344 | SAS | BEB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03834 | hp2 | a0001 | c0001 | t0010 | g0087 | SAS | BEB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | BEB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | BEB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0019 | SAS | BEB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0185 | SAS | STU | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG04199 | hp2 | a0003 | c0004 | t0002 | g0336 | SAS | STU | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | STU | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | STU | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG04228 | hp1 | a0002 | c0003 | t0001 | g0243 | SAS | STU | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | YRI | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18612 | hp2 | a0002 | c0003 | t0001 | g0154 | EAS | CHB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | CHB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | YRI | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18942 | hp1 | a0004 | c0006 | t0001 | g0234 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18945 | hp1 | a0001 | c0001 | t0008 | g0070 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18949 | hp1 | a0001 | c0008 | t0001 | g0310 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18949 | hp2 | a0002 | c0017 | t0001 | g0169 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18951 | hp2 | a0002 | c0003 | t0001 | g0150 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18954 | hp1 | a0002 | c0003 | t0001 | g0147 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18954 | hp2 | a0004 | c0006 | t0001 | g0236 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18957 | hp1 | a0002 | c0003 | t0001 | g0160 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18960 | hp2 | a0004 | c0006 | t0001 | g0235 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18962 | hp2 | a0004 | c0006 | t0001 | g0228 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18965 | hp2 | a0001 | c0005 | t0001 | g0259 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18970 | hp1 | a0001 | c0012 | t0001 | g0251 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18971 | hp2 | a0001 | c0005 | t0001 | g0256 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0155 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18974 | hp1 | a0001 | c0005 | t0001 | g0250 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18978 | hp2 | a0004 | c0006 | t0001 | g0237 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18982 | hp1 | a0002 | c0003 | t0003 | g0136 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18988 | hp1 | a0003 | c0004 | t0002 | g0329 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18989 | hp1 | a0002 | c0003 | t0001 | g0156 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18990 | hp1 | a0002 | c0003 | t0001 | g0146 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18991 | hp2 | a0002 | c0003 | t0001 | g0170 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18993 | hp1 | a0005 | c0009 | t0001 | g0361 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18993 | hp2 | a0001 | c0008 | t0001 | g0312 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18994 | hp1 | a0001 | c0005 | t0001 | g0254 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18995 | hp2 | a0001 | c0005 | t0001 | g0002 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19000 | hp2 | a0004 | c0006 | t0001 | g0232 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19001 | hp2 | a0002 | c0003 | t0001 | g0145 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19002 | hp2 | a0002 | c0003 | t0001 | g0149 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19005 | hp2 | a0001 | c0005 | t0001 | g0258 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19007 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19009 | hp2 | a0001 | c0005 | t0001 | g0348 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19010 | hp1 | a0003 | c0004 | t0002 | g0332 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19011 | hp1 | a0003 | c0004 | t0002 | g0328 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | LWK | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19054 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19057 | hp1 | a0002 | c0003 | t0001 | g0140 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19057 | hp2 | a0004 | c0006 | t0001 | g0233 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19066 | hp2 | a0002 | c0003 | t0001 | g0144 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19067 | hp2 | a0003 | c0004 | t0002 | g0022 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19068 | hp2 | a0001 | c0005 | t0001 | g0002 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19072 | hp2 | a0002 | c0003 | t0001 | g0159 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19076 | hp1 | a0001 | c0019 | t0001 | g0212 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19076 | hp2 | a0003 | c0004 | t0002 | g0331 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19078 | hp1 | a0005 | c0009 | t0001 | g0362 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19078 | hp2 | a0001 | c0005 | t0001 | g0255 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19080 | hp1 | a0001 | c0005 | t0001 | g0252 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | YRI | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0132 | AFR | ASW | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ASW | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0016 | EUR | TSI | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0278 | EUR | TSI | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA20805 | hp2 | a0003 | c0004 | t0002 | g0128 | EUR | TSI | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | GIH | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | GIH | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02486 | hp2 | a0002 | c0003 | t0003 | g0355 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | USA | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | USA | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18955 | hp1 | a0002 | c0003 | t0001 | g0143 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA20300 | hp1 | a0002 | c0003 | t0003 | g0353 | AFR | USA | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| homoSapiens | chm13v2 | a0003 | c0004 | t0002 | g0343 | REF | REF | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0003 | g0351 | REF | REF | ESF1_chr20_13709325_13789919 | ESF1 | chr20 | 13709325 | 13789919 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:13714960 | T | G | 1 | a0003 | 22 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(19): Show |
missense_variant | MODERATE | c.2470A>C | p.Ile824Leu | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 14/14 | 2553/3188 | 2470/2556 | 824/851 | chr20 | 13714960 | |||
| chr20:13715115 | T | C | 1 | a0012 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.2315A>G | p.Asn772Ser | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 14/14 | 2398/3188 | 2315/2556 | 772/851 | chr20 | 13715115 | |||
| chr20:13759718 | A | G | 1 | a0007 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.1802T>C | p.Met601Thr | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/14 | 1885/3188 | 1802/2556 | 601/851 | chr20 | 13759718 | |||
| chr20:13759800 | CCTT | C | 1 | a0004 | 10 | HG00621.hp1 HG02165.hp1 HG02523.hp2 others(7): Show |
conservative_inframe_deletion | MODERATE | c.1717_1719delAAG | p.Lys573del | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/14 | 1802/3188 | 1717/2556 | 573/851 | chr20 | 13759800 | |||
| chr20:13766794 | A | G | 10 | a0001 a0003 a0004 others(7): Show |
328 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
missense_variant | MODERATE | c.1649T>C | p.Ile550Thr | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/14 | 1732/3188 | 1649/2556 | 550/851 | chr20 | 13766794 | |||
| chr20:13772587 | C | T | 1 | a0013 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.1178G>A | p.Arg393Lys | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 5/14 | 1261/3188 | 1178/2556 | 393/851 | chr20 | 13772587 | |||
| chr20:13775270 | T | C | 1 | a0005 | 2 | NA18993.hp1 NA19078.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1036A>G | p.Ile346Val | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/14 | 1119/3188 | 1036/2556 | 346/851 | chr20 | 13775270 | |||
| chr20:13775893 | C | A | 1 | a0009 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.1015G>T | p.Asp339Tyr | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 3/14 | 1098/3188 | 1015/2556 | 339/851 | chr20 | 13775893 | |||
| chr20:13782597 | C | T | 1 | a0008 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.544G>A | p.Glu182Lys | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/14 | 627/3188 | 544/2556 | 182/851 | chr20 | 13782597 | |||
| chr20:13782617 | T | C | 1 | a0010 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.524A>G | p.His175Arg | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/14 | 607/3188 | 524/2556 | 175/851 | chr20 | 13782617 | |||
| chr20:13782880 | T | G | 1 | a0006 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.261A>C | p.Lys87Asn | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/14 | 344/3188 | 261/2556 | 87/851 | chr20 | 13782880 | |||
| chr20:13783047 | C | T | 1 | a0011 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.94G>A | p.Val32Ile | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/14 | 177/3188 | 94/2556 | 32/851 | chr20 | 13783047 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:13715033 | C | T | 6 | a0001c0002 a0001c0019 a0004c0006 others(3): Show |
94 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(91): Show |
synonymous_variant | LOW | c.2397G>A | p.Arg799Arg | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 14/14 | 2480/3188 | 2397/2556 | 799/851 | chr20 | 13715033 | |||
| chr20:13717482 | G | A | 2 | a0001c0008 a0002c0017 |
3 | NA18949.hp1 NA18949.hp2 NA18993.hp2 |
synonymous_variant | LOW | c.2148C>T | p.Asp716Asp | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/14 | 2231/3188 | 2148/2556 | 716/851 | chr20 | 13717482 | |||
| chr20:13728421 | A | T | 1 | a0011c0011 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.1995T>A | p.Val665Val | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/14 | 2078/3188 | 1995/2556 | 665/851 | chr20 | 13728421 | |||
| chr20:13759702 | T | C | 1 | a0001c0012 | 1 | NA18970.hp1 | synonymous_variant | LOW | c.1818A>G | p.Lys606Lys | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/14 | 1901/3188 | 1818/2556 | 606/851 | chr20 | 13759702 | |||
| chr20:13776146 | T | C | 1 | a0001c0007 | 3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.762A>G | p.Glu254Glu | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 3/14 | 845/3188 | 762/2556 | 254/851 | chr20 | 13776146 | |||
| chr20:13776263 | T | C | 1 | a0001c0019 | 1 | NA19076.hp1 | synonymous_variant | LOW | c.645A>G | p.Gln215Gln | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 3/14 | 728/3188 | 645/2556 | 215/851 | chr20 | 13776263 | |||
| chr20:13782955 | A | G | 2 | a0001c0005 a0001c0012 |
15 | HG00408.hp2 HG01496.hp2 HG02040.hp1 others(12): Show |
synonymous_variant | LOW | c.186T>C | p.His62His | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/14 | 269/3188 | 186/2556 | 62/851 | chr20 | 13782955 | |||
| chr20:13783108 | C | T | 1 | a0002c0010 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.33G>A | p.Gln11Gln | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/14 | 116/3188 | 33/2556 | 11/851 | chr20 | 13783108 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:13714328 | A | G | 1 | a0001c0001t0008 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*546T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 14/14 | 546 | chr20 | 13714328 | ||||||
| chr20:13714337 | A | G | 1 | a0002c0003t0007 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*537T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 14/14 | 537 | chr20 | 13714337 | ||||||
| chr20:13714349 | A | G | 1 | a0001c0001t0004 | 6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*525T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 14/14 | 525 | chr20 | 13714349 | ||||||
| chr20:13714419 | G | A | 1 | a0001c0001t0009 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*455C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 14/14 | 455 | chr20 | 13714419 | ||||||
| chr20:13714420 | C | A | 1 | a0001c0001t0009 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*454G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 14/14 | 454 | chr20 | 13714420 | ||||||
| chr20:13714611 | T | A | 1 | a0001c0001t0010 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*263A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 14/14 | 263 | chr20 | 13714611 | ||||||
| chr20:13714650 | T | C | 1 | a0001c0001t0006 | 3 | HG03195.hp2 HG03486.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*224A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 14/14 | 224 | chr20 | 13714650 | ||||||
| chr20:13714714 | A | G | 1 | a0001c0001t0005 | 4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*160T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 14/14 | 160 | chr20 | 13714714 | ||||||
| chr20:13714817 | T | C | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(24): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(370): Show |
3_prime_UTR_variant | MODIFIER | c.*57A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 14/14 | 57 | chr20 | 13714817 | ||||||
| chr20:13714851 | G | A | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0007t0002 others(2): Show |
45 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*23C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 14/14 | 23 | chr20 | 13714851 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:13715177 | C | CA | 26 | a0001c0001t0001g0108 a0001c0001t0001g0306 a0001c0001t0002g0116 others(23): Show |
27 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.2263-11dupT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13715177 | |||||||
| chr20:13715197 | A | T | 2 | a0001c0001t0001g0322 a0001c0001t0002g0239 |
2 | HG02004.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2263-30T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13715197 | |||||||
| chr20:13715411 | T | C | 1 | a0013c0014t0001g0364 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2263-244A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13715411 | |||||||
| chr20:13715482 | G | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(295): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.2263-315C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13715482 | |||||||
| chr20:13715514 | G | A | 2 | a0001c0001t0001g0242 a0010c0020t0001g0131 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2263-347C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13715514 | |||||||
| chr20:13715578 | T | C | 2 | a0001c0008t0001g0310 a0001c0008t0001g0312 |
2 | NA18949.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.2263-411A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13715578 | |||||||
| chr20:13715711 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2263-544G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13715711 | |||||||
| chr20:13715792 | C | T | 42 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(39): Show |
45 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.2263-625G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13715792 | |||||||
| chr20:13716034 | A | G | 1 | a0003c0004t0002g0224 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2263-867T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716034 | |||||||
| chr20:13716046 | G | A | 2 | a0001c0002t0001g0271 a0001c0002t0001g0274 |
2 | NA19077.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2263-879C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716046 | |||||||
| chr20:13716134 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2263-967T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716134 | |||||||
| chr20:13716158 | C | T | 4 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2263-991G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716158 | |||||||
| chr20:13716190 | T | G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG02055.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2263-1023A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716190 | |||||||
| chr20:13716284 | AG | A | 42 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(39): Show |
45 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.2262+1083delC | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716284 | |||||||
| chr20:13716487 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2262+881A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716487 | |||||||
| chr20:13716642 | C | CT | 16 | a0001c0001t0001g0114 a0001c0001t0001g0297 a0001c0001t0001g0306 others(13): Show |
17 | HG00741.hp2 HG01081.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.2262+725dupA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716642 | |||||||
| chr20:13716804 | A | AT | 6 | a0001c0001t0001g0281 a0001c0001t0002g0095 a0001c0001t0002g0102 others(3): Show |
6 | HG00741.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2262+563dupA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTT | 6 | a0001c0001t0001g0018 a0001c0001t0001g0264 a0001c0001t0001g0285 others(3): Show |
9 | HG00140.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2262+561_2262+563d others(5): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTT | 5 | a0001c0001t0001g0020 a0001c0001t0001g0260 a0001c0001t0002g0101 others(2): Show |
6 | HG00280.hp2 HG00323.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2262+559_2262+563d others(7): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(1): Show |
11 | a0001c0001t0001g0261 a0001c0001t0001g0319 a0001c0001t0001g0321 others(8): Show |
11 | HG01258.hp2 HG01361.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.2262+556_2262+563d others(10): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(2): Show |
7 | a0001c0001t0001g0209 a0001c0001t0001g0324 a0001c0001t0001g0325 others(4): Show |
7 | HG01928.hp2 HG01975.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.2262+555_2262+563d others(11): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(3): Show |
3 | a0002c0003t0001g0248 a0004c0006t0001g0230 a0013c0014t0001g0364 |
3 | HG01169.hp2 HG02523.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2262+554_2262+563d others(12): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(4): Show |
7 | a0001c0001t0001g0240 a0001c0001t0001g0313 a0001c0002t0001g0174 others(4): Show |
7 | HG01071.hp2 HG01167.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.2262+553_2262+563d others(13): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0311 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2262+552_2262+563d others(14): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(6): Show |
3 | a0001c0001t0001g0297 a0001c0001t0001g0317 a0001c0002t0001g0181 |
3 | HG01081.hp1 HG03831.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.2262+551_2262+563d others(15): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(7): Show |
5 | a0001c0001t0001g0299 a0001c0001t0001g0314 a0001c0002t0001g0205 others(2): Show |
5 | NA18747.hp1 NA18945.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.2262+550_2262+563d others(16): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(8): Show |
5 | a0001c0001t0001g0305 a0001c0001t0001g0318 a0001c0001t0001g0347 others(2): Show |
6 | HG01109.hp2 HG02155.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.2262+549_2262+563d others(17): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(9): Show |
6 | a0001c0001t0001g0301 a0001c0002t0001g0196 a0001c0002t0001g0199 others(3): Show |
6 | HG00733.hp2 NA18946.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.2262+548_2262+563d others(18): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(10): Show |
16 | a0001c0001t0001g0045 a0001c0001t0001g0300 a0001c0001t0001g0306 others(13): Show |
16 | HG00323.hp2 HG00609.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.2262+547_2262+563d others(19): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(11): Show |
4 | a0001c0001t0001g0322 a0001c0002t0001g0188 a0005c0009t0001g0361 others(1): Show |
4 | HG02004.hp1 NA18975.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2262+546_2262+563d others(20): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(12): Show |
3 | a0001c0001t0001g0296 a0001c0001t0001g0309 a0001c0002t0001g0195 |
3 | HG00735.hp2 HG03491.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.2262+545_2262+563d others(21): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(13): Show |
7 | a0001c0001t0001g0304 a0001c0002t0001g0200 a0001c0002t0001g0204 others(4): Show |
7 | HG00408.hp1 HG01515.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.2262+544_2262+563d others(22): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(14): Show |
1 | a0001c0001t0001g0316 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2262+543_2262+563d others(23): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(15): Show |
1 | a0002c0003t0001g0163 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2262+542_2262+563d others(24): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(16): Show |
4 | a0001c0001t0001g0263 a0001c0008t0001g0310 a0002c0003t0001g0146 others(1): Show |
4 | HG00544.hp1 HG02818.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.2262+541_2262+563d others(25): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(17): Show |
3 | a0002c0003t0001g0012 a0002c0003t0001g0143 a0002c0003t0001g0148 |
4 | HG02165.hp2 NA18955.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.2262+540_2262+563d others(26): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(18): Show |
2 | a0001c0001t0001g0303 a0002c0003t0001g0144 |
2 | HG03239.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2262+539_2262+563d others(27): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(19): Show |
2 | a0001c0001t0001g0221 a0001c0002t0001g0194 |
2 | HG02083.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2262+538_2262+563d others(28): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(21): Show |
2 | a0001c0001t0001g0298 a0001c0008t0001g0312 |
2 | HG03927.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.2262+536_2262+563d others(30): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(23): Show |
1 | a0001c0002t0001g0173 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2262+534_2262+563d others(32): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | A | ATTTTTTT others(26): Show |
1 | a0001c0002t0001g0203 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2262+563_2262+564i others(35): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | AT | A | 5 | a0001c0001t0001g0315 a0001c0001t0002g0239 a0002c0003t0001g0013 others(2): Show |
6 | HG01934.hp2 HG01978.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.2262+563delA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | ATTT | A | 8 | a0001c0001t0001g0346 a0002c0003t0001g0132 a0002c0003t0001g0151 others(5): Show |
8 | HG00738.hp2 HG01175.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2262+561_2262+563d others(5): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | ATTTT | A | 8 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0003c0004t0002g0286 others(5): Show |
8 | HG00423.hp2 HG00735.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2262+560_2262+563d others(6): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | ATTTTT | A | 23 | a0001c0001t0001g0223 a0001c0001t0002g0100 a0001c0001t0002g0116 others(20): Show |
24 | HG00597.hp2 HG00733.hp1 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.2262+559_2262+563d others(7): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | ATTTTTT | A | 21 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0219 others(18): Show |
25 | HG00408.hp2 HG00642.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.2262+558_2262+563d others(8): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | ATTTTTTT others(1): Show |
A | 31 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0030 others(28): Show |
32 | HG00597.hp1 HG00673.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.2262+556_2262+563d others(10): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | ATTTTTTT others(2): Show |
A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
97 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.2262+555_2262+563d others(11): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | ATTTTTTT others(3): Show |
A | 8 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(5): Show |
8 | HG00621.hp1 HG01109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2262+554_2262+563d others(12): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | ATTTTTTT others(4): Show |
A | 6 | a0002c0003t0003g0134 a0002c0003t0003g0135 a0002c0003t0003g0136 others(3): Show |
6 | HG00280.hp1 HG00642.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.2262+553_2262+563d others(13): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | ATTTTTTT others(5): Show |
A | 3 | a0001c0001t0009g0216 a0001c0002t0001g0182 a0001c0002t0001g0184 |
3 | HG02683.hp2 NA19006.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2262+552_2262+563d others(14): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | ATTTTTTT others(6): Show |
A | 14 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(11): Show |
16 | HG01261.hp2 HG02055.hp1 HG03579.hp2 others(13): Show |
intron_variant | MODIFIER | c.2262+551_2262+563d others(15): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | ATTTTTTT others(8): Show |
A | 3 | a0001c0007t0002g0017 a0001c0007t0002g0238 a0010c0020t0001g0131 |
4 | HG02145.hp2 HG02257.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2262+549_2262+563d others(17): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716804 | ATTTTTTT others(11): Show |
A | 3 | a0001c0001t0001g0292 a0001c0001t0001g0302 a0001c0001t0001g0308 |
3 | NA18956.hp2 NA18990.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2262+546_2262+563d others(20): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716804 | |||||||
| chr20:13716836 | T | A | 4 | a0001c0001t0002g0239 a0001c0007t0002g0017 a0001c0007t0002g0238 others(1): Show |
5 | HG02257.hp2 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2262+532A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716836 | |||||||
| chr20:13716837 | A | G | 1 | a0001c0002t0001g0180 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2262+531T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716837 | |||||||
| chr20:13716885 | T | A | 25 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(22): Show |
26 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.2262+483A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13716885 | |||||||
| chr20:13717019 | G | A | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2262+349C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13717019 | |||||||
| chr20:13717160 | G | A | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2262+208C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13717160 | |||||||
| chr20:13717163 | G | A | 21 | a0003c0004t0002g0022 a0003c0004t0002g0128 a0003c0004t0002g0224 others(18): Show |
22 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.2262+205C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13717163 | |||||||
| chr20:13717164 | C | A | 21 | a0003c0004t0002g0022 a0003c0004t0002g0128 a0003c0004t0002g0224 others(18): Show |
22 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.2262+204G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13717164 | |||||||
| chr20:13717210 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2262+158C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13717210 | |||||||
| chr20:13717359 | T | C | 355 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(352): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.2262+9A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 13/13 | chr20 | 13717359 | |||||||
| chr20:13717736 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2116-222C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 12/13 | chr20 | 13717736 | |||||||
| chr20:13717943 | A | G | 347 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(344): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(370): Show |
intron_variant | MODIFIER | c.2116-429T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 12/13 | chr20 | 13717943 | |||||||
| chr20:13718091 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2116-577C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 12/13 | chr20 | 13718091 | |||||||
| chr20:13718098 | C | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2116-584G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 12/13 | chr20 | 13718098 | |||||||
| chr20:13718238 | C | A | 25 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(22): Show |
26 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.2115+670G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 12/13 | chr20 | 13718238 | |||||||
| chr20:13718634 | G | A | 85 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(82): Show |
90 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.2115+274C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 12/13 | chr20 | 13718634 | |||||||
| chr20:13718703 | G | A | 2 | a0001c0002t0001g0183 a0001c0002t0001g0202 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2115+205C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 12/13 | chr20 | 13718703 | |||||||
| chr20:13718753 | C | CATAAAAA others(16): Show |
61 | a0001c0001t0001g0018 a0001c0001t0001g0111 a0001c0001t0001g0112 others(58): Show |
64 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.2115+154_2115+155i others(25): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 12/13 | chr20 | 13718753 | |||||||
| chr20:13718753 | C | CATAAAAA others(17): Show |
1 | a0001c0001t0001g0300 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2115+154_2115+155i others(26): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 12/13 | chr20 | 13718753 | |||||||
| chr20:13718754 | T | A | 62 | a0001c0001t0001g0018 a0001c0001t0001g0111 a0001c0001t0001g0112 others(59): Show |
65 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.2115+154A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 12/13 | chr20 | 13718754 | |||||||
| chr20:13719143 | G | A | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2039-159C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13719143 | |||||||
| chr20:13719398 | G | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(344): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(370): Show |
intron_variant | MODIFIER | c.2039-414C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13719398 | |||||||
| chr20:13719400 | A | T | 4 | a0002c0003t0003g0135 a0002c0003t0003g0136 a0002c0003t0003g0357 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2039-416T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13719400 | |||||||
| chr20:13719443 | G | A | 1 | a0001c0002t0001g0272 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2039-459C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13719443 | |||||||
| chr20:13719467 | A | C | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2039-483T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13719467 | |||||||
| chr20:13719502 | A | G | 63 | a0001c0001t0001g0018 a0001c0001t0001g0111 a0001c0001t0001g0112 others(60): Show |
66 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.2039-518T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13719502 | |||||||
| chr20:13719521 | C | T | 63 | a0001c0001t0001g0018 a0001c0001t0001g0111 a0001c0001t0001g0112 others(60): Show |
66 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.2039-537G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13719521 | |||||||
| chr20:13719581 | G | GA | 85 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(82): Show |
90 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.2039-598dupT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13719581 | |||||||
| chr20:13719633 | G | A | 1 | a0001c0001t0005g0123 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2039-649C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13719633 | |||||||
| chr20:13719704 | A | G | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2039-720T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13719704 | |||||||
| chr20:13719894 | A | C | 1 | a0001c0001t0001g0026 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2039-910T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13719894 | |||||||
| chr20:13719967 | C | T | 2 | a0001c0001t0001g0314 a0001c0001t0001g0318 |
2 | NA18747.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2039-983G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13719967 | |||||||
| chr20:13720127 | A | G | 85 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(82): Show |
90 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.2039-1143T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13720127 | |||||||
| chr20:13720237 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
162 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.2039-1253A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13720237 | |||||||
| chr20:13720277 | G | A | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.2039-1293C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13720277 | |||||||
| chr20:13720552 | A | G | 1 | a0002c0003t0001g0246 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2039-1568T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13720552 | |||||||
| chr20:13720626 | C | A | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2039-1642G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13720626 | |||||||
| chr20:13720714 | A | G | 103 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0209 others(100): Show |
113 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2039-1730T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13720714 | |||||||
| chr20:13720749 | G | GT | 2 | a0001c0001t0004g0010 a0001c0001t0004g0126 |
3 | HG02886.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2039-1766dupA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13720749 | |||||||
| chr20:13720839 | G | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
77 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.2039-1855C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13720839 | |||||||
| chr20:13720847 | G | A | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(259): Show |
283 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.2039-1863C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13720847 | |||||||
| chr20:13720892 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2039-1908C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13720892 | |||||||
| chr20:13720899 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2039-1915A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13720899 | |||||||
| chr20:13720991 | C | T | 1 | a0001c0002t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2039-2007G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13720991 | |||||||
| chr20:13721372 | T | C | 1 | a0001c0007t0002g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2039-2388A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13721372 | |||||||
| chr20:13721388 | G | A | 97 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0264 others(94): Show |
107 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.2039-2404C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13721388 | |||||||
| chr20:13721552 | G | A | 1 | a0002c0003t0001g0161 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2039-2568C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13721552 | |||||||
| chr20:13721678 | C | T | 1 | a0010c0020t0001g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2039-2694G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13721678 | |||||||
| chr20:13721935 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(259): Show |
283 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.2039-2951A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13721935 | |||||||
| chr20:13722004 | T | C | 102 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0217 others(99): Show |
112 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.2039-3020A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13722004 | |||||||
| chr20:13722106 | T | A | 1 | a0001c0001t0001g0031 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2039-3122A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13722106 | |||||||
| chr20:13722159 | C | A | 1 | a0001c0001t0001g0041 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2039-3175G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13722159 | |||||||
| chr20:13722304 | TC | T | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2039-3321delG | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13722304 | |||||||
| chr20:13722466 | A | G | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2039-3482T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13722466 | |||||||
| chr20:13722478 | T | C | 1 | a0001c0001t0004g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2039-3494A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13722478 | |||||||
| chr20:13722642 | G | C | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.2039-3658C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13722642 | |||||||
| chr20:13722687 | A | AT | 86 | a0001c0001t0001g0300 a0001c0001t0002g0095 a0001c0001t0002g0096 others(83): Show |
91 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2039-3704dupA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13722687 | |||||||
| chr20:13722687 | A | T | 1 | a0010c0020t0001g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2039-3703T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13722687 | |||||||
| chr20:13722837 | CAG | C | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2039-3855_2039-385 others(6): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13722837 | |||||||
| chr20:13723040 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
94 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.2039-4056G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723040 | |||||||
| chr20:13723081 | G | C | 92 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(89): Show |
97 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.2039-4097C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723081 | |||||||
| chr20:13723082 | T | C | 1 | a0002c0003t0001g0168 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2039-4098A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723082 | |||||||
| chr20:13723101 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG02148.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2039-4117G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723101 | |||||||
| chr20:13723175 | G | C | 1 | a0010c0020t0001g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2039-4191C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723175 | |||||||
| chr20:13723234 | G | C | 1 | a0001c0001t0001g0313 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2039-4250C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723234 | |||||||
| chr20:13723246 | G | A | 1 | a0001c0002t0001g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2039-4262C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723246 | |||||||
| chr20:13723300 | G | A | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.2039-4316C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723300 | |||||||
| chr20:13723333 | G | T | 25 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(22): Show |
26 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.2039-4349C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723333 | |||||||
| chr20:13723369 | C | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(259): Show |
283 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.2039-4385G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723369 | |||||||
| chr20:13723452 | G | A | 2 | a0004c0006t0001g0235 a0004c0006t0001g0237 |
2 | NA18960.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.2039-4468C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723452 | |||||||
| chr20:13723498 | T | TCCTAGAT others(302): Show |
5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2039-4515_2039-451 others(313): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723498 | |||||||
| chr20:13723498 | T | TCCTAGAT others(302): Show |
51 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(48): Show |
53 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.2039-4515_2039-451 others(313): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723498 | |||||||
| chr20:13723498 | T | TCCTAGAT others(307): Show |
1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2039-4515_2039-451 others(318): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723498 | |||||||
| chr20:13723498 | T | TCCTAGAT others(308): Show |
7 | a0001c0001t0002g0239 a0001c0007t0002g0017 a0001c0007t0002g0238 others(4): Show |
8 | HG00423.hp2 HG00597.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2039-4515_2039-451 others(319): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723498 | |||||||
| chr20:13723498 | T | TCCTAGAT others(309): Show |
14 | a0003c0004t0002g0022 a0003c0004t0002g0224 a0003c0004t0002g0286 others(11): Show |
15 | HG00733.hp1 HG00735.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.2039-4515_2039-451 others(320): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723498 | |||||||
| chr20:13723498 | T | TCCTAGAT others(310): Show |
6 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(3): Show |
6 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2039-4515_2039-451 others(321): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723498 | |||||||
| chr20:13723498 | T | TCCTAGAT others(309): Show |
1 | a0003c0004t0002g0342 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2039-4515_2039-451 others(320): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723498 | |||||||
| chr20:13723601 | C | G | 1 | a0001c0002t0001g0191 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2039-4617G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723601 | |||||||
| chr20:13723736 | C | T | 2 | a0001c0001t0001g0346 a0001c0001t0001g0347 |
2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2038+4642G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723736 | |||||||
| chr20:13723835 | T | C | 3 | a0001c0001t0001g0265 a0001c0001t0002g0119 a0001c0002t0001g0225 |
3 | HG02486.hp1 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2038+4543A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723835 | |||||||
| chr20:13723927 | T | C | 2 | a0001c0001t0001g0040 a0011c0011t0002g0241 |
2 | HG02717.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.2038+4451A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13723927 | |||||||
| chr20:13724065 | C | T | 1 | a0002c0003t0001g0146 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2038+4313G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13724065 | |||||||
| chr20:13724070 | G | A | 4 | a0001c0001t0002g0239 a0001c0002t0001g0280 a0001c0007t0002g0017 others(1): Show |
5 | HG00741.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2038+4308C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13724070 | |||||||
| chr20:13724252 | G | A | 9 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(6): Show |
9 | HG00280.hp1 HG00621.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.2038+4126C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13724252 | |||||||
| chr20:13724306 | TAAATAAA others(4): Show |
T | 106 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0209 others(103): Show |
117 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.2038+4061_2038+407 others(15): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13724306 | |||||||
| chr20:13724397 | T | C | 13 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(10): Show |
14 | HG00741.hp2 HG02258.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2038+3981A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13724397 | |||||||
| chr20:13724414 | A | G | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2038+3964T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13724414 | |||||||
| chr20:13724603 | T | C | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.2038+3775A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13724603 | |||||||
| chr20:13724627 | T | A | 4 | a0001c0001t0002g0239 a0001c0007t0002g0017 a0001c0007t0002g0238 others(1): Show |
5 | HG02257.hp2 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2038+3751A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13724627 | |||||||
| chr20:13724714 | T | A | 1 | a0001c0002t0001g0289 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2038+3664A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13724714 | |||||||
| chr20:13724762 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2038+3616A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13724762 | |||||||
| chr20:13724924 | C | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(259): Show |
283 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.2038+3454G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13724924 | |||||||
| chr20:13724989 | G | A | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2038+3389C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13724989 | |||||||
| chr20:13725069 | T | C | 1 | a0002c0017t0001g0169 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2038+3309A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13725069 | |||||||
| chr20:13725326 | T | C | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2038+3052A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13725326 | |||||||
| chr20:13725351 | C | T | 1 | a0002c0003t0003g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2038+3027G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13725351 | |||||||
| chr20:13725514 | T | C | 1 | a0001c0002t0001g0191 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2038+2864A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13725514 | |||||||
| chr20:13725545 | T | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0285 |
2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2038+2833A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13725545 | |||||||
| chr20:13725735 | T | G | 1 | a0001c0002t0001g0275 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2038+2643A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13725735 | |||||||
| chr20:13725781 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(273): Show |
298 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.2038+2597T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13725781 | |||||||
| chr20:13726073 | C | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2038+2305G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13726073 | |||||||
| chr20:13726077 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0073 others(2): Show |
6 | HG00544.hp2 HG02523.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.2038+2301G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13726077 | |||||||
| chr20:13726228 | C | T | 21 | a0003c0004t0002g0022 a0003c0004t0002g0128 a0003c0004t0002g0224 others(18): Show |
22 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.2038+2150G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13726228 | |||||||
| chr20:13726432 | C | A | 1 | a0004c0006t0001g0232 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2038+1946G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13726432 | |||||||
| chr20:13726549 | A | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG02572.hp2 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2038+1829T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13726549 | |||||||
| chr20:13726655 | C | A | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.2038+1723G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13726655 | |||||||
| chr20:13726747 | C | T | 304 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(301): Show |
328 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.2038+1631G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13726747 | |||||||
| chr20:13726832 | TCAAAA | T | 7 | a0002c0003t0003g0349 a0002c0003t0003g0350 a0002c0003t0003g0352 others(4): Show |
7 | HG02486.hp2 HG02970.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2038+1541_2038+154 others(9): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13726832 | |||||||
| chr20:13726933 | C | G | 4 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2038+1445G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13726933 | |||||||
| chr20:13727047 | C | T | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2038+1331G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13727047 | |||||||
| chr20:13727096 | A | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0059 others(1): Show |
5 | NA18998.hp2 NA19001.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.2038+1282T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13727096 | |||||||
| chr20:13727104 | C | G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG02055.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2038+1274G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13727104 | |||||||
| chr20:13727155 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(273): Show |
298 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.2038+1223A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13727155 | |||||||
| chr20:13727441 | T | C | 1 | a0001c0002t0001g0275 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2038+937A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13727441 | |||||||
| chr20:13727610 | G | A | 2 | a0005c0009t0001g0361 a0005c0009t0001g0362 |
2 | NA18993.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.2038+768C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13727610 | |||||||
| chr20:13727670 | C | T | 14 | a0001c0002t0001g0014 a0001c0002t0001g0023 a0001c0002t0001g0172 others(11): Show |
16 | HG01261.hp2 NA18952.hp2 NA18959.hp1 others(13): Show |
intron_variant | MODIFIER | c.2038+708G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13727670 | |||||||
| chr20:13727718 | G | A | 1 | a0002c0003t0001g0158 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2038+660C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13727718 | |||||||
| chr20:13727895 | T | C | 346 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(343): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(369): Show |
intron_variant | MODIFIER | c.2038+483A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13727895 | |||||||
| chr20:13728023 | A | G | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2038+355T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13728023 | |||||||
| chr20:13728030 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0052 |
2 | NA18942.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2038+348C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13728030 | |||||||
| chr20:13728141 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(273): Show |
298 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.2038+237A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13728141 | |||||||
| chr20:13728149 | A | G | 42 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(39): Show |
45 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.2038+229T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 11/13 | chr20 | 13728149 | |||||||
| chr20:13728527 | C | G | 1 | a0001c0001t0004g0124 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1951-62G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13728527 | |||||||
| chr20:13728550 | T | C | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1951-85A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13728550 | |||||||
| chr20:13728554 | A | G | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1951-89T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13728554 | |||||||
| chr20:13728708 | T | C | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1951-243A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13728708 | |||||||
| chr20:13728733 | G | A | 1 | a0001c0001t0004g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1951-268C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13728733 | |||||||
| chr20:13728760 | G | A | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1951-295C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13728760 | |||||||
| chr20:13728778 | A | G | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1951-313T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13728778 | |||||||
| chr20:13728815 | C | T | 1 | a0002c0003t0001g0161 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1951-350G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13728815 | |||||||
| chr20:13728866 | C | CA | 10 | a0001c0001t0002g0239 a0001c0001t0005g0122 a0002c0003t0003g0133 others(7): Show |
10 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1951-402dupT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13728866 | |||||||
| chr20:13728944 | A | C | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1951-479T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13728944 | |||||||
| chr20:13728952 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1951-487A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13728952 | |||||||
| chr20:13729230 | T | G | 1 | a0001c0001t0001g0295 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1951-765A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13729230 | |||||||
| chr20:13729328 | A | C | 286 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(283): Show |
309 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.1951-863T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13729328 | |||||||
| chr20:13729335 | G | C | 1 | a0001c0001t0001g0091 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1951-870C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13729335 | |||||||
| chr20:13729457 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1951-992C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13729457 | |||||||
| chr20:13729514 | G | A | 7 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(4): Show |
7 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1951-1049C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13729514 | |||||||
| chr20:13729535 | G | A | 1 | a0001c0012t0001g0251 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1951-1070C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13729535 | |||||||
| chr20:13729589 | T | C | 13 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(10): Show |
13 | HG00741.hp2 HG01515.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1951-1124A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13729589 | |||||||
| chr20:13729605 | A | C | 1 | a0001c0001t0001g0265 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1951-1140T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13729605 | |||||||
| chr20:13729644 | TAAAGA | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1951-1184_1951-118 others(9): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13729644 | |||||||
| chr20:13729653 | G | T | 4 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
4 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1951-1188C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13729653 | |||||||
| chr20:13729684 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(244): Show |
268 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.1951-1219G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13729684 | |||||||
| chr20:13730019 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1951-1554T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13730019 | |||||||
| chr20:13730078 | C | CT | 12 | a0001c0001t0001g0025 a0001c0001t0001g0054 a0001c0001t0001g0346 others(9): Show |
12 | HG02486.hp1 HG02559.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1951-1614dupA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13730078 | |||||||
| chr20:13730127 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1951-1662G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13730127 | |||||||
| chr20:13730230 | A | C | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1951-1765T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13730230 | |||||||
| chr20:13730385 | C | CT | 24 | a0001c0001t0001g0034 a0001c0001t0001g0045 a0001c0001t0001g0062 others(21): Show |
24 | HG00597.hp1 HG00741.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.1951-1921dupA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13730385 | |||||||
| chr20:13730447 | G | A | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1951-1982C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13730447 | |||||||
| chr20:13730484 | T | A | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1951-2019A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13730484 | |||||||
| chr20:13730489 | T | C | 1 | a0001c0005t0001g0253 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1951-2024A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13730489 | |||||||
| chr20:13730577 | G | T | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1951-2112C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13730577 | |||||||
| chr20:13730630 | C | T | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1951-2165G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13730630 | |||||||
| chr20:13730703 | A | AT | 26 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0260 others(23): Show |
28 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.1951-2239dupA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13730703 | |||||||
| chr20:13730760 | A | G | 20 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(17): Show |
22 | HG00741.hp2 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1951-2295T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13730760 | |||||||
| chr20:13730788 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1951-2323G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13730788 | |||||||
| chr20:13731132 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | HG02809.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1950+2589G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13731132 | |||||||
| chr20:13731138 | T | C | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1950+2583A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13731138 | |||||||
| chr20:13731208 | G | A | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1950+2513C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13731208 | |||||||
| chr20:13731459 | G | A | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1950+2262C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13731459 | |||||||
| chr20:13731531 | CA | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.1950+2189delT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13731531 | |||||||
| chr20:13731531 | CAA | C | 26 | a0001c0001t0001g0315 a0001c0001t0001g0327 a0001c0001t0004g0124 others(23): Show |
26 | HG00280.hp1 HG00642.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.1950+2188_1950+218 others(6): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13731531 | |||||||
| chr20:13731531 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1950+2177_1950+218 others(17): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13731531 | |||||||
| chr20:13731531 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1950+2176_1950+218 others(18): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13731531 | |||||||
| chr20:13731717 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1950+2004A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13731717 | |||||||
| chr20:13731746 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
94 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1950+1975G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13731746 | |||||||
| chr20:13731747 | T | C | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1950+1974A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13731747 | |||||||
| chr20:13732106 | A | G | 355 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(352): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.1950+1615T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732106 | |||||||
| chr20:13732181 | A | G | 2 | a0001c0001t0001g0265 a0001c0002t0001g0225 |
2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1950+1540T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732181 | |||||||
| chr20:13732256 | G | A | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1950+1465C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732256 | |||||||
| chr20:13732280 | G | T | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1950+1441C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732280 | |||||||
| chr20:13732306 | A | G | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1950+1415T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732306 | |||||||
| chr20:13732310 | T | C | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1950+1411A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732310 | |||||||
| chr20:13732337 | A | C | 20 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(17): Show |
22 | HG00741.hp2 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1950+1384T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732337 | |||||||
| chr20:13732464 | G | A | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1950+1257C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732464 | |||||||
| chr20:13732578 | G | C | 1 | a0003c0004t0002g0334 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1950+1143C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732578 | |||||||
| chr20:13732855 | G | A | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1950+866C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732855 | |||||||
| chr20:13732903 | C | CTTAT | 8 | a0001c0001t0005g0122 a0001c0005t0001g0256 a0001c0005t0001g0258 others(5): Show |
8 | HG02486.hp2 HG02970.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.1950+814_1950+817d others(6): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732903 | |||||||
| chr20:13732903 | C | CTTATTTA others(1): Show |
4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0123 others(1): Show |
4 | HG00597.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1950+810_1950+817d others(10): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732903 | |||||||
| chr20:13732903 | CTTAT | C | 27 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(24): Show |
31 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1950+814_1950+817d others(6): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732903 | |||||||
| chr20:13732903 | CTTATTTA others(1): Show |
C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
262 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.1950+810_1950+817d others(10): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732903 | |||||||
| chr20:13732903 | CTTATTTA others(5): Show |
C | 19 | a0001c0001t0002g0095 a0002c0003t0001g0012 a0002c0003t0001g0143 others(16): Show |
20 | HG00544.hp1 HG00621.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1950+806_1950+817d others(14): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13732903 | |||||||
| chr20:13733002 | C | G | 2 | a0004c0006t0001g0228 a0004c0006t0001g0232 |
2 | NA18962.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1950+719G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13733002 | |||||||
| chr20:13733075 | G | A | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(2): Show |
5 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1950+646C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13733075 | |||||||
| chr20:13733099 | C | CATTTTTT others(201): Show |
1 | a0001c0001t0002g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1950+621_1950+622i others(210): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13733099 | |||||||
| chr20:13733099 | C | CATTTTTT others(202): Show |
3 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 |
3 | HG02486.hp1 HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1950+621_1950+622i others(211): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13733099 | |||||||
| chr20:13733113 | G | A | 4 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1950+608C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13733113 | |||||||
| chr20:13733115 | A | G | 4 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1950+606T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13733115 | |||||||
| chr20:13733194 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0068 |
2 | NA18991.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1950+527G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13733194 | |||||||
| chr20:13733292 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1950+429A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13733292 | |||||||
| chr20:13733384 | T | A | 1 | a0001c0001t0001g0066 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1950+337A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13733384 | |||||||
| chr20:13733398 | T | C | 1 | a0002c0003t0001g0244 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1950+323A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13733398 | |||||||
| chr20:13733462 | G | A | 104 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0115 others(101): Show |
114 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1950+259C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13733462 | |||||||
| chr20:13733473 | G | A | 98 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0209 others(95): Show |
108 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1950+248C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13733473 | |||||||
| chr20:13733682 | G | C | 1 | a0003c0004t0002g0329 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1950+39C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 10/13 | chr20 | 13733682 | |||||||
| chr20:13733966 | A | G | 2 | a0001c0001t0005g0122 a0001c0001t0005g0123 |
2 | HG03704.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1829-124T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13733966 | |||||||
| chr20:13734049 | A | G | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1829-207T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13734049 | |||||||
| chr20:13734326 | G | C | 20 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(17): Show |
22 | HG00741.hp2 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1829-484C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13734326 | |||||||
| chr20:13734416 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1829-574A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13734416 | |||||||
| chr20:13734740 | T | C | 95 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(92): Show |
101 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1829-898A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13734740 | |||||||
| chr20:13734778 | A | AT | 296 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(293): Show |
320 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.1829-937_1829-936i others(3): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13734778 | |||||||
| chr20:13735044 | T | C | 7 | a0002c0003t0001g0157 a0002c0003t0001g0243 a0002c0003t0001g0244 others(4): Show |
7 | HG00673.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1829-1202A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13735044 | |||||||
| chr20:13735131 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1829-1289G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13735131 | |||||||
| chr20:13735242 | C | G | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1829-1400G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13735242 | |||||||
| chr20:13735412 | T | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0264 |
5 | HG02258.hp1 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1829-1570A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13735412 | |||||||
| chr20:13735696 | G | C | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1829-1854C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13735696 | |||||||
| chr20:13735854 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1829-2012G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13735854 | |||||||
| chr20:13735946 | C | A | 1 | a0001c0001t0008g0070 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1829-2104G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13735946 | |||||||
| chr20:13736180 | T | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0078 a0001c0001t0001g0083 others(3): Show |
6 | HG01167.hp2 HG02145.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1829-2338A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13736180 | |||||||
| chr20:13736246 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1829-2404G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13736246 | |||||||
| chr20:13736257 | T | C | 20 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(17): Show |
22 | HG00741.hp2 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1829-2415A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13736257 | |||||||
| chr20:13736303 | A | G | 1 | a0001c0002t0001g0191 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1829-2461T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13736303 | |||||||
| chr20:13736323 | T | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
95 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1829-2481A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13736323 | |||||||
| chr20:13736379 | A | G | 3 | a0002c0003t0001g0132 a0002c0003t0001g0153 a0002c0003t0001g0158 |
3 | HG00738.hp2 HG01256.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1829-2537T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13736379 | |||||||
| chr20:13736411 | G | A | 10 | a0001c0001t0002g0239 a0001c0001t0004g0010 a0001c0001t0004g0124 others(7): Show |
11 | HG02258.hp2 HG02559.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1829-2569C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13736411 | |||||||
| chr20:13736710 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1829-2868C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13736710 | |||||||
| chr20:13736753 | A | T | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1829-2911T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13736753 | |||||||
| chr20:13736809 | TACA | T | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1829-2970_1829-296 others(7): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13736809 | |||||||
| chr20:13736817 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0093 |
2 | HG03927.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1829-2975A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13736817 | |||||||
| chr20:13736869 | C | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
7 | HG03654.hp2 NA18946.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.1829-3027G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13736869 | |||||||
| chr20:13737080 | GAC | G | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1829-3240_1829-323 others(6): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737080 | |||||||
| chr20:13737178 | T | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
7 | HG03654.hp2 NA18946.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.1829-3336A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737178 | |||||||
| chr20:13737179 | G | C | 1 | a0002c0003t0003g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1829-3337C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737179 | |||||||
| chr20:13737588 | T | G | 1 | a0002c0003t0003g0135 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1829-3746A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737588 | |||||||
| chr20:13737724 | G | C | 1 | a0010c0020t0001g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1829-3882C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737724 | |||||||
| chr20:13737739 | C | T | 16 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(13): Show |
16 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1829-3897G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737739 | |||||||
| chr20:13737752 | C | T | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1829-3910G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737752 | |||||||
| chr20:13737756 | C | T | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1829-3914G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737756 | |||||||
| chr20:13737820 | A | AT | 22 | a0001c0001t0009g0216 a0003c0004t0002g0022 a0003c0004t0002g0128 others(19): Show |
23 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1829-3979dupA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737820 | |||||||
| chr20:13737828 | T | C | 1 | a0001c0002t0001g0214 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1829-3986A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737828 | |||||||
| chr20:13737969 | G | A | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-4127C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737969 | |||||||
| chr20:13737973 | T | C | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-4131A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737973 | |||||||
| chr20:13737974 | T | G | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-4132A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737974 | |||||||
| chr20:13737975 | T | C | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-4133A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737975 | |||||||
| chr20:13737976 | T | G | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-4134A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737976 | |||||||
| chr20:13737977 | A | T | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-4135T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737977 | |||||||
| chr20:13737978 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1829-4136C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737978 | |||||||
| chr20:13737979 | A | T | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-4137T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737979 | |||||||
| chr20:13737980 | G | T | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-4138C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737980 | |||||||
| chr20:13737997 | G | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
159 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1829-4155C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737997 | |||||||
| chr20:13737998 | C | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
159 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1829-4156G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13737998 | |||||||
| chr20:13738117 | T | C | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1829-4275A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13738117 | |||||||
| chr20:13738250 | G | T | 355 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(352): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.1829-4408C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13738250 | |||||||
| chr20:13738284 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1829-4442A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13738284 | |||||||
| chr20:13738317 | C | CT | 333 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(330): Show |
358 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(355): Show |
intron_variant | MODIFIER | c.1829-4476dupA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13738317 | |||||||
| chr20:13738317 | C | CTT | 13 | a0001c0001t0001g0265 a0001c0001t0002g0239 a0001c0001t0004g0010 others(10): Show |
14 | HG01433.hp1 HG01928.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.1829-4477_1829-447 others(6): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13738317 | |||||||
| chr20:13738408 | G | A | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1829-4566C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13738408 | |||||||
| chr20:13738411 | T | C | 1 | a0001c0002t0001g0200 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1829-4569A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13738411 | |||||||
| chr20:13738564 | T | A | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1829-4722A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13738564 | |||||||
| chr20:13738597 | G | A | 1 | a0010c0020t0001g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1829-4755C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13738597 | |||||||
| chr20:13738745 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | HG02809.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1829-4903A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13738745 | |||||||
| chr20:13738791 | C | T | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1829-4949G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13738791 | |||||||
| chr20:13738792 | G | A | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1829-4950C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13738792 | |||||||
| chr20:13738826 | TATAA | T | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1829-4988_1829-498 others(8): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13738826 | |||||||
| chr20:13739086 | T | C | 1 | a0001c0002t0001g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1829-5244A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13739086 | |||||||
| chr20:13739225 | G | C | 20 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(17): Show |
22 | HG00741.hp2 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1829-5383C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13739225 | |||||||
| chr20:13739583 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1829-5741G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13739583 | |||||||
| chr20:13739721 | C | CA | 24 | a0001c0001t0001g0219 a0001c0001t0002g0095 a0001c0001t0002g0096 others(21): Show |
26 | HG00621.hp2 HG00741.hp2 HG02135.hp1 others(23): Show |
intron_variant | MODIFIER | c.1829-5880dupT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13739721 | |||||||
| chr20:13739721 | CA | C | 10 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0103 others(7): Show |
10 | HG01167.hp1 HG01975.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1829-5880delT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13739721 | |||||||
| chr20:13739754 | A | G | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0264 others(5): Show |
12 | HG02258.hp1 HG02280.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1829-5912T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13739754 | |||||||
| chr20:13739959 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1829-6117A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13739959 | |||||||
| chr20:13740176 | T | C | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1829-6334A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13740176 | |||||||
| chr20:13740326 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
94 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1829-6484A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13740326 | |||||||
| chr20:13740475 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1829-6633C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13740475 | |||||||
| chr20:13740518 | C | G | 63 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(60): Show |
67 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1829-6676G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13740518 | |||||||
| chr20:13740571 | G | A | 1 | a0003c0004t0002g0128 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1829-6729C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13740571 | |||||||
| chr20:13740736 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1829-6894T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13740736 | |||||||
| chr20:13740991 | AT | A | 59 | a0001c0001t0001g0209 a0001c0002t0001g0014 a0001c0002t0001g0015 others(56): Show |
63 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1829-7150delA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13740991 | |||||||
| chr20:13741023 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1829-7181C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13741023 | |||||||
| chr20:13741148 | A | G | 4 | a0003c0004t0002g0022 a0003c0004t0002g0332 a0003c0004t0002g0333 others(1): Show |
5 | HG00423.hp2 HG00597.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.1829-7306T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13741148 | |||||||
| chr20:13741171 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1829-7329G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13741171 | |||||||
| chr20:13741298 | A | C | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1829-7456T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13741298 | |||||||
| chr20:13741319 | T | C | 4 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
4 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1829-7477A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13741319 | |||||||
| chr20:13741358 | AC | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(275): Show |
300 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.1829-7517delG | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13741358 | |||||||
| chr20:13741466 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1829-7624G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13741466 | |||||||
| chr20:13742014 | G | T | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1829-8172C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13742014 | |||||||
| chr20:13742187 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
94 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1829-8345G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13742187 | |||||||
| chr20:13742197 | T | A | 1 | a0001c0001t0001g0242 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1829-8355A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13742197 | |||||||
| chr20:13742210 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1829-8368A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13742210 | |||||||
| chr20:13742224 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1829-8382G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13742224 | |||||||
| chr20:13742338 | T | C | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1829-8496A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13742338 | |||||||
| chr20:13742341 | T | C | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1829-8499A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13742341 | |||||||
| chr20:13742355 | C | A | 7 | a0001c0001t0001g0223 a0001c0001t0001g0321 a0001c0001t0001g0322 others(4): Show |
7 | HG01928.hp2 HG01934.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1829-8513G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13742355 | |||||||
| chr20:13742356 | C | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1829-8514G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13742356 | |||||||
| chr20:13743011 | C | A | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1829-9169G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743011 | |||||||
| chr20:13743089 | T | C | 1 | a0001c0002t0001g0188 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1829-9247A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743089 | |||||||
| chr20:13743146 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1829-9304T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743146 | |||||||
| chr20:13743180 | T | A | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-9338A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743180 | |||||||
| chr20:13743182 | A | T | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-9340T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743182 | |||||||
| chr20:13743184 | A | G | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-9342T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743184 | |||||||
| chr20:13743186 | C | T | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-9344G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743186 | |||||||
| chr20:13743188 | A | G | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-9346T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743188 | |||||||
| chr20:13743189 | T | C | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-9347A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743189 | |||||||
| chr20:13743194 | A | T | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-9352T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743194 | |||||||
| chr20:13743195 | G | T | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1829-9353C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743195 | |||||||
| chr20:13743234 | T | A | 347 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(344): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(370): Show |
intron_variant | MODIFIER | c.1829-9392A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743234 | |||||||
| chr20:13743338 | C | A | 304 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(301): Show |
328 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.1829-9496G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743338 | |||||||
| chr20:13743385 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1829-9543A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743385 | |||||||
| chr20:13743441 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
94 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1829-9599G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743441 | |||||||
| chr20:13743549 | CA | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(276): Show |
301 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1829-9708delT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743549 | |||||||
| chr20:13743609 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | NA18952.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1829-9767G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743609 | |||||||
| chr20:13743642 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1829-9800C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743642 | |||||||
| chr20:13743643 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1829-9801A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743643 | |||||||
| chr20:13743656 | T | C | 1 | a0003c0004t0002g0338 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1829-9814A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743656 | |||||||
| chr20:13743716 | C | T | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1829-9874G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743716 | |||||||
| chr20:13743933 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1829-10091T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743933 | |||||||
| chr20:13743936 | G | T | 1 | a0001c0002t0001g0272 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1829-10094C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743936 | |||||||
| chr20:13743946 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1829-10104A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13743946 | |||||||
| chr20:13744116 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
6 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1829-10274C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13744116 | |||||||
| chr20:13744181 | T | C | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1829-10339A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13744181 | |||||||
| chr20:13744281 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
94 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1829-10439C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13744281 | |||||||
| chr20:13744370 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1829-10528A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13744370 | |||||||
| chr20:13744582 | T | C | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1829-10740A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13744582 | |||||||
| chr20:13744592 | T | A | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1829-10750A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13744592 | |||||||
| chr20:13744824 | C | A | 1 | a0001c0002t0001g0272 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1829-10982G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13744824 | |||||||
| chr20:13744869 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0073 others(2): Show |
6 | HG00544.hp2 HG02523.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1829-11027G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13744869 | |||||||
| chr20:13745009 | A | T | 105 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0209 others(102): Show |
115 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1829-11167T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13745009 | |||||||
| chr20:13745322 | G | A | 1 | a0003c0004t0002g0022 | 2 | HG02027.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1829-11480C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13745322 | |||||||
| chr20:13745331 | T | C | 1 | a0001c0001t0001g0294 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1829-11489A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13745331 | |||||||
| chr20:13745350 | A | C | 1 | a0001c0002t0001g0182 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1829-11508T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13745350 | |||||||
| chr20:13745485 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1829-11643A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13745485 | |||||||
| chr20:13745530 | C | T | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1829-11688G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13745530 | |||||||
| chr20:13745544 | C | T | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1829-11702G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13745544 | |||||||
| chr20:13745562 | C | T | 1 | a0001c0001t0006g0003 | 3 | HG03195.hp2 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1829-11720G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13745562 | |||||||
| chr20:13745785 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1829-11943T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13745785 | |||||||
| chr20:13745909 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1829-12067C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13745909 | |||||||
| chr20:13745910 | GA | G | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1829-12069delT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13745910 | |||||||
| chr20:13745982 | A | T | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1829-12140T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13745982 | |||||||
| chr20:13745994 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
95 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1829-12152C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13745994 | |||||||
| chr20:13746537 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1829-12695G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13746537 | |||||||
| chr20:13746731 | A | G | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1829-12889T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13746731 | |||||||
| chr20:13746777 | C | T | 1 | a0001c0002t0001g0267 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1828+12915G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13746777 | |||||||
| chr20:13746878 | G | C | 7 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0311 others(4): Show |
7 | HG00423.hp1 NA18747.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1828+12814C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13746878 | |||||||
| chr20:13747081 | T | A | 1 | a0001c0001t0001g0069 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1828+12611A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13747081 | |||||||
| chr20:13747093 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
159 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1828+12599G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13747093 | |||||||
| chr20:13747217 | T | C | 355 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(352): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.1828+12475A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13747217 | |||||||
| chr20:13747261 | TA | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(274): Show |
297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.1828+12430delT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13747261 | |||||||
| chr20:13747432 | A | G | 347 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(344): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(370): Show |
intron_variant | MODIFIER | c.1828+12260T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13747432 | |||||||
| chr20:13747559 | A | T | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+12133T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13747559 | |||||||
| chr20:13747593 | G | GA | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
99 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1828+12098dupT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13747593 | |||||||
| chr20:13747673 | G | T | 1 | a0001c0001t0001g0057 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1828+12019C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13747673 | |||||||
| chr20:13747821 | T | C | 3 | a0001c0001t0001g0292 a0001c0001t0001g0302 a0001c0001t0001g0308 |
3 | NA18956.hp2 NA18990.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1828+11871A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13747821 | |||||||
| chr20:13747834 | G | A | 20 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(17): Show |
22 | HG00741.hp2 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1828+11858C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13747834 | |||||||
| chr20:13747913 | A | C | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1828+11779T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13747913 | |||||||
| chr20:13747941 | A | G | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+11751T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13747941 | |||||||
| chr20:13747958 | C | A | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1828+11734G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13747958 | |||||||
| chr20:13747984 | T | C | 2 | a0002c0003t0003g0354 a0012c0016t0003g0356 |
2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1828+11708A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13747984 | |||||||
| chr20:13748132 | C | T | 1 | a0001c0001t0001g0007 | 2 | HG00544.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1828+11560G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748132 | |||||||
| chr20:13748203 | A | G | 304 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(301): Show |
328 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.1828+11489T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748203 | |||||||
| chr20:13748381 | C | T | 1 | a0002c0003t0003g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1828+11311G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748381 | |||||||
| chr20:13748403 | T | TATATACA others(11): Show |
233 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
253 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.1828+11271_1828+11 others(24): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748403 | |||||||
| chr20:13748411 | C | CAT | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1828+11279_1828+11 others(8): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748411 | |||||||
| chr20:13748419 | T | TACATATA others(11): Show |
1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1828+11272_1828+11 others(24): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748419 | |||||||
| chr20:13748437 | T | TACATATA others(1): Show |
23 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0049 others(20): Show |
24 | HG00741.hp2 HG01175.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.1828+11254_1828+11 others(14): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748437 | |||||||
| chr20:13748437 | TAC | T | 68 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0221 others(65): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1828+11253_1828+11 others(8): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748437 | |||||||
| chr20:13748441 | C | T | 23 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0049 others(20): Show |
24 | HG00741.hp2 HG01175.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.1828+11251G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748441 | |||||||
| chr20:13748447 | T | C | 68 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0221 others(65): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1828+11245A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748447 | |||||||
| chr20:13748451 | T | C | 23 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0049 others(20): Show |
24 | HG00741.hp2 HG01175.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.1828+11241A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748451 | |||||||
| chr20:13748461 | T | C | 68 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0221 others(65): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1828+11231A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748461 | |||||||
| chr20:13748467 | C | T | 80 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0221 others(77): Show |
84 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1828+11225G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748467 | |||||||
| chr20:13748468 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1828+11224T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748468 | |||||||
| chr20:13748469 | C | CAT | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1828+11221_1828+11 others(8): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748469 | |||||||
| chr20:13748477 | C | T | 68 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0221 others(65): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1828+11215G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748477 | |||||||
| chr20:13748479 | C | CAT | 4 | a0001c0001t0002g0239 a0001c0007t0002g0017 a0001c0007t0002g0238 others(1): Show |
5 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1828+11211_1828+11 others(8): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748479 | |||||||
| chr20:13748479 | C | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1828+11213G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748479 | |||||||
| chr20:13748479 | CATATACA others(13): Show |
C | 1 | a0003c0004t0002g0338 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1828+11193_1828+11 others(26): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748479 | |||||||
| chr20:13748485 | C | T | 81 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0221 others(78): Show |
84 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1828+11207G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748485 | |||||||
| chr20:13748487 | C | T | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1828+11205G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748487 | |||||||
| chr20:13748489 | T | C | 80 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0221 others(77): Show |
83 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1828+11203A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748489 | |||||||
| chr20:13748495 | T | C | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1828+11197A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748495 | |||||||
| chr20:13748497 | C | CACAT | 12 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(9): Show |
12 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1828+11194_1828+11 others(10): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748497 | |||||||
| chr20:13748497 | C | CATATATA others(5): Show |
1 | a0004c0006t0001g0230 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1828+11183_1828+11 others(18): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748497 | |||||||
| chr20:13748499 | T | C | 68 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0221 others(65): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1828+11193A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748499 | |||||||
| chr20:13748503 | TACAC | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1828+11185_1828+11 others(10): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748503 | |||||||
| chr20:13748505 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1828+11187G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748505 | |||||||
| chr20:13748507 | C | T | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0099 others(7): Show |
10 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1828+11185G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748507 | |||||||
| chr20:13748509 | T | C | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+11183A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748509 | |||||||
| chr20:13748515 | T | C | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1828+11177A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748515 | |||||||
| chr20:13748517 | C | CATATAT | 60 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0221 others(57): Show |
63 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.1828+11174_1828+11 others(12): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748517 | |||||||
| chr20:13748517 | CACATATA others(37): Show |
C | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1828+11131_1828+11 others(50): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748517 | |||||||
| chr20:13748519 | C | T | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+11173G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748519 | |||||||
| chr20:13748521 | T | C | 61 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0221 others(58): Show |
64 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1828+11171A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748521 | |||||||
| chr20:13748521 | TATATATA others(5): Show |
T | 1 | a0001c0001t0009g0216 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1828+11159_1828+11 others(18): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748521 | |||||||
| chr20:13748529 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1828+11163A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748529 | |||||||
| chr20:13748533 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1828+11159G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748533 | |||||||
| chr20:13748535 | T | C | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+11157A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748535 | |||||||
| chr20:13748540 | A | G | 2 | a0001c0001t0001g0291 a0001c0001t0009g0216 |
2 | HG02683.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1828+11152T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748540 | |||||||
| chr20:13748540 | ATGTG | A | 3 | a0001c0001t0002g0239 a0001c0001t0004g0010 a0001c0001t0004g0126 |
4 | HG02559.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1828+11148_1828+11 others(10): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748540 | |||||||
| chr20:13748540 | ATGTGTGT others(1): Show |
A | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+11144_1828+11 others(14): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748540 | |||||||
| chr20:13748544 | GTGTGTA | G | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1828+11142_1828+11 others(12): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748544 | |||||||
| chr20:13748546 | G | A | 11 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(8): Show |
11 | HG00741.hp2 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1828+11146C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748546 | |||||||
| chr20:13748548 | G | A | 11 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(8): Show |
11 | HG00741.hp2 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1828+11144C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748548 | |||||||
| chr20:13748550 | A | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(281): Show |
306 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.1828+11142T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748550 | |||||||
| chr20:13748552 | A | G | 17 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0111 others(14): Show |
21 | HG01515.hp1 HG01516.hp2 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.1828+11140T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748552 | |||||||
| chr20:13748555 | T | C | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+11137A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748555 | |||||||
| chr20:13748556 | A | G | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1828+11136T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748556 | |||||||
| chr20:13748557 | T | C | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+11135A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748557 | |||||||
| chr20:13748562 | ATATGTGT others(26): Show |
A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(63): Show |
72 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1828+11097_1828+11 others(39): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748562 | |||||||
| chr20:13748564 | ATGTGTG | A | 72 | a0001c0001t0001g0018 a0001c0001t0001g0221 a0001c0001t0001g0222 others(69): Show |
75 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.1828+11122_1828+11 others(12): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748564 | |||||||
| chr20:13748564 | ATGTGTGT others(3): Show |
A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0044 others(13): Show |
17 | HG00733.hp2 HG01071.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1828+11118_1828+11 others(16): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748564 | |||||||
| chr20:13748566 | G | A | 176 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(173): Show |
188 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1828+11126C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748566 | |||||||
| chr20:13748568 | G | A | 45 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0111 others(42): Show |
50 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1828+11124C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748568 | |||||||
| chr20:13748568 | GTGTGTGT others(1): Show |
G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0038 others(83): Show |
91 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1828+11116_1828+11 others(14): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748568 | |||||||
| chr20:13748570 | G | A | 54 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0111 others(51): Show |
61 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.1828+11122C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748570 | |||||||
| chr20:13748570 | GTGTGTA | G | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | HG02809.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1828+11116_1828+11 others(12): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748570 | |||||||
| chr20:13748572 | G | A | 100 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0221 others(97): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1828+11120C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748572 | |||||||
| chr20:13748574 | G | A | 49 | a0001c0001t0001g0220 a0001c0001t0001g0282 a0001c0001t0001g0293 others(46): Show |
52 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.1828+11118C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748574 | |||||||
| chr20:13748578 | A | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0044 others(13): Show |
17 | HG00733.hp2 HG01071.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1828+11114T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748578 | |||||||
| chr20:13748580 | A | G | 2 | a0001c0001t0001g0282 a0001c0001t0002g0100 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1828+11112T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748580 | |||||||
| chr20:13748582 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1828+11110T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748582 | |||||||
| chr20:13748585 | TATATATA | T | 7 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0264 others(4): Show |
9 | HG02055.hp1 HG02280.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1828+11100_1828+11 others(13): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748585 | |||||||
| chr20:13748588 | A | ATTTTT | 3 | a0001c0001t0005g0120 a0001c0001t0005g0122 a0001c0001t0005g0123 |
3 | HG03704.hp2 NA18970.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1828+11103_1828+11 others(11): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748588 | |||||||
| chr20:13748588 | A | T | 4 | a0001c0001t0004g0127 a0002c0003t0001g0243 a0002c0003t0001g0246 others(1): Show |
4 | HG02717.hp1 HG03017.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1828+11104T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748588 | |||||||
| chr20:13748588 | ATATATTT | A | 8 | a0003c0004t0002g0128 a0003c0004t0002g0224 a0003c0004t0002g0329 others(5): Show |
8 | HG00423.hp2 HG01943.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1828+11097_1828+11 others(13): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748588 | |||||||
| chr20:13748590 | A | T | 44 | a0001c0001t0004g0127 a0001c0001t0005g0120 a0001c0001t0005g0121 others(41): Show |
47 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1828+11102T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748590 | |||||||
| chr20:13748590 | ATATTTTT | A | 12 | a0003c0004t0002g0022 a0003c0004t0002g0286 a0003c0004t0002g0287 others(9): Show |
13 | HG00597.hp2 HG00733.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1828+11095_1828+11 others(13): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748590 | |||||||
| chr20:13748590 | ATATTTTT others(2): Show |
A | 7 | a0001c0001t0001g0220 a0001c0001t0001g0293 a0001c0001t0001g0294 others(4): Show |
7 | HG01934.hp1 NA18960.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1828+11093_1828+11 others(15): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748590 | |||||||
| chr20:13748591 | TA | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0079 a0001c0001t0001g0083 others(1): Show |
5 | HG01167.hp2 HG02109.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1828+11100delT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748591 | |||||||
| chr20:13748592 | A | ATATATAT others(7): Show |
1 | a0001c0001t0004g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1828+11099_1828+11 others(20): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748592 | |||||||
| chr20:13748592 | A | ATATATTT others(7): Show |
1 | a0001c0001t0004g0010 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1828+11099_1828+11 others(20): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748592 | |||||||
| chr20:13748592 | A | T | 57 | a0001c0001t0004g0127 a0001c0001t0005g0120 a0001c0001t0005g0121 others(54): Show |
60 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1828+11100T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748592 | |||||||
| chr20:13748592 | AT | A | 12 | a0001c0001t0001g0036 a0001c0001t0001g0044 a0001c0001t0001g0046 others(9): Show |
12 | HG00733.hp2 HG01071.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1828+11099delA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748592 | |||||||
| chr20:13748592 | ATTT | A | 90 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0038 others(87): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1828+11097_1828+11 others(9): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748592 | |||||||
| chr20:13748592 | ATTTTT | A | 71 | a0001c0001t0001g0018 a0001c0001t0001g0221 a0001c0001t0001g0222 others(68): Show |
74 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.1828+11095_1828+11 others(11): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748592 | |||||||
| chr20:13748593 | T | TATA | 4 | a0001c0001t0002g0095 a0001c0001t0002g0097 a0001c0001t0002g0098 others(1): Show |
4 | HG00741.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1828+11098_1828+11 others(9): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748593 | |||||||
| chr20:13748594 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1828+11098A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748594 | |||||||
| chr20:13748599 | T | A | 54 | a0001c0001t0001g0018 a0001c0001t0001g0221 a0001c0001t0001g0222 others(51): Show |
57 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1828+11093A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748599 | |||||||
| chr20:13748663 | C | A | 1 | a0001c0001t0001g0057 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1828+11029G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748663 | |||||||
| chr20:13748709 | C | T | 1 | a0001c0002t0001g0181 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1828+10983G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748709 | |||||||
| chr20:13748823 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1828+10869C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748823 | |||||||
| chr20:13748862 | A | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(344): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(370): Show |
intron_variant | MODIFIER | c.1828+10830T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748862 | |||||||
| chr20:13748886 | C | A | 1 | a0001c0001t0001g0309 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1828+10806G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748886 | |||||||
| chr20:13748896 | C | A | 304 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(301): Show |
328 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.1828+10796G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13748896 | |||||||
| chr20:13749232 | A | AT | 213 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(210): Show |
231 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1828+10459dupA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749232 | |||||||
| chr20:13749232 | A | ATT | 46 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0038 others(43): Show |
46 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.1828+10458_1828+10 others(8): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749232 | |||||||
| chr20:13749232 | AT | A | 16 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0111 others(13): Show |
20 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1828+10459delA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749232 | |||||||
| chr20:13749232 | ATT | A | 43 | a0001c0001t0001g0281 a0001c0001t0001g0284 a0002c0003t0001g0012 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1828+10458_1828+10 others(8): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749232 | |||||||
| chr20:13749232 | ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0002g0239 a0003c0004t0002g0337 |
2 | HG02559.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1828+10448_1828+10 others(18): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749232 | |||||||
| chr20:13749232 | ATTTTTTT others(6): Show |
A | 19 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(16): Show |
21 | HG00741.hp2 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1828+10447_1828+10 others(19): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749232 | |||||||
| chr20:13749251 | TTTTTTTT others(3): Show |
T | 1 | a0001c0002t0001g0181 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1828+10431_1828+10 others(16): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749251 | |||||||
| chr20:13749258 | T | C | 32 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0111 others(29): Show |
38 | HG00741.hp2 HG01515.hp1 HG01517.hp2 others(35): Show |
intron_variant | MODIFIER | c.1828+10434A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749258 | |||||||
| chr20:13749275 | A | G | 355 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(352): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.1828+10417T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749275 | |||||||
| chr20:13749286 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
159 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1828+10406T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749286 | |||||||
| chr20:13749658 | C | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(281): Show |
306 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.1828+10034G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749658 | |||||||
| chr20:13749719 | C | A | 97 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0218 others(94): Show |
103 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1828+9973G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749719 | |||||||
| chr20:13749721 | A | G | 1 | a0001c0002t0001g0214 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1828+9971T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749721 | |||||||
| chr20:13749863 | G | A | 4 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1828+9829C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749863 | |||||||
| chr20:13749866 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1828+9826G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749866 | |||||||
| chr20:13749909 | C | T | 19 | a0003c0004t0002g0022 a0003c0004t0002g0128 a0003c0004t0002g0224 others(16): Show |
20 | HG00423.hp2 HG00597.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1828+9783G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749909 | |||||||
| chr20:13749919 | C | A | 1 | a0001c0001t0001g0324 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1828+9773G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13749919 | |||||||
| chr20:13750046 | G | A | 4 | a0003c0004t0002g0022 a0003c0004t0002g0332 a0003c0004t0002g0333 others(1): Show |
5 | HG00423.hp2 HG00597.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.1828+9646C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750046 | |||||||
| chr20:13750119 | G | T | 1 | a0001c0001t0001g0242 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1828+9573C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750119 | |||||||
| chr20:13750125 | A | T | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+9567T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750125 | |||||||
| chr20:13750149 | C | T | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1828+9543G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750149 | |||||||
| chr20:13750155 | G | T | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1828+9537C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750155 | |||||||
| chr20:13750169 | A | G | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1828+9523T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750169 | |||||||
| chr20:13750193 | A | T | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1828+9499T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750193 | |||||||
| chr20:13750223 | G | A | 1 | a0003c0004t0002g0128 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1828+9469C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750223 | |||||||
| chr20:13750429 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
288 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.1828+9263G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750429 | |||||||
| chr20:13750492 | G | A | 347 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(344): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(370): Show |
intron_variant | MODIFIER | c.1828+9200C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750492 | |||||||
| chr20:13750505 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1828+9187C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750505 | |||||||
| chr20:13750556 | T | C | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+9136A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750556 | |||||||
| chr20:13750641 | C | T | 355 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(352): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.1828+9051G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750641 | |||||||
| chr20:13750673 | C | T | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+9019G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750673 | |||||||
| chr20:13750752 | G | A | 1 | a0003c0004t0002g0331 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1828+8940C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750752 | |||||||
| chr20:13750753 | A | G | 1 | a0003c0004t0002g0331 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1828+8939T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750753 | |||||||
| chr20:13750905 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1828+8787G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13750905 | |||||||
| chr20:13751166 | A | G | 25 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(22): Show |
26 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.1828+8526T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13751166 | |||||||
| chr20:13751192 | A | C | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1828+8500T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13751192 | |||||||
| chr20:13751194 | C | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
159 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1828+8498G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13751194 | |||||||
| chr20:13751362 | C | A | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1828+8330G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13751362 | |||||||
| chr20:13751567 | G | C | 355 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(352): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.1828+8125C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13751567 | |||||||
| chr20:13751568 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
289 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.1828+8124C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13751568 | |||||||
| chr20:13751573 | T | C | 1 | a0003c0004t0002g0331 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1828+8119A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13751573 | |||||||
| chr20:13751573 | T | G | 24 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(21): Show |
25 | HG00423.hp2 HG00597.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.1828+8119A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13751573 | |||||||
| chr20:13751856 | G | A | 2 | a0001c0001t0001g0282 a0001c0001t0001g0285 |
2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1828+7836C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13751856 | |||||||
| chr20:13751922 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | HG02809.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1828+7770C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13751922 | |||||||
| chr20:13751947 | A | G | 8 | a0001c0005t0001g0002 a0001c0005t0001g0252 a0001c0005t0001g0253 others(5): Show |
10 | HG00408.hp2 HG02155.hp1 NA18965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1828+7745T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13751947 | |||||||
| chr20:13751956 | C | T | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+7736G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13751956 | |||||||
| chr20:13751984 | T | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(300): Show |
327 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.1828+7708A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13751984 | |||||||
| chr20:13751989 | C | T | 1 | a0002c0003t0003g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1828+7703G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13751989 | |||||||
| chr20:13752181 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1828+7511G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13752181 | |||||||
| chr20:13752188 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1828+7504G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13752188 | |||||||
| chr20:13752200 | T | C | 2 | a0001c0002t0001g0173 a0001c0002t0001g0203 |
2 | NA19062.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1828+7492A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13752200 | |||||||
| chr20:13752230 | G | A | 1 | a0002c0003t0001g0149 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1828+7462C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13752230 | |||||||
| chr20:13752416 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1828+7276C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13752416 | |||||||
| chr20:13752692 | T | C | 1 | a0001c0002t0001g0203 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1828+7000A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13752692 | |||||||
| chr20:13752911 | C | A | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1828+6781G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13752911 | |||||||
| chr20:13753002 | A | G | 1 | a0002c0003t0001g0143 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1828+6690T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13753002 | |||||||
| chr20:13753084 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
94 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1828+6608C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13753084 | |||||||
| chr20:13753086 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1828+6606G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13753086 | |||||||
| chr20:13753195 | A | G | 1 | a0002c0003t0001g0160 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1828+6497T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13753195 | |||||||
| chr20:13753386 | T | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
4 | HG02258.hp1 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1828+6306A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13753386 | |||||||
| chr20:13753475 | C | A | 1 | a0001c0001t0001g0294 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1828+6217G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13753475 | |||||||
| chr20:13753632 | C | T | 95 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0218 others(92): Show |
101 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1828+6060G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13753632 | |||||||
| chr20:13753873 | T | C | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1828+5819A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13753873 | |||||||
| chr20:13754088 | G | T | 1 | a0001c0001t0002g0102 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1828+5604C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13754088 | |||||||
| chr20:13754106 | T | C | 11 | a0001c0001t0001g0222 a0001c0001t0001g0300 a0001c0001t0001g0301 others(8): Show |
11 | HG00423.hp1 HG03942.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.1828+5586A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13754106 | |||||||
| chr20:13754252 | C | T | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+5440G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13754252 | |||||||
| chr20:13754261 | C | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0285 |
2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1828+5431G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13754261 | |||||||
| chr20:13754504 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1828+5188A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13754504 | |||||||
| chr20:13754535 | G | GTCTA | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+5153_1828+515 others(8): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13754535 | |||||||
| chr20:13754598 | C | T | 12 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0111 others(9): Show |
16 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1828+5094G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13754598 | |||||||
| chr20:13754827 | A | C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0111 others(12): Show |
20 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1828+4865T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13754827 | |||||||
| chr20:13754974 | C | T | 304 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(301): Show |
328 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.1828+4718G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13754974 | |||||||
| chr20:13755054 | T | C | 355 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(352): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.1828+4638A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13755054 | |||||||
| chr20:13755074 | C | T | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1828+4618G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13755074 | |||||||
| chr20:13755141 | C | T | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1828+4551G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13755141 | |||||||
| chr20:13755165 | G | A | 1 | a0001c0005t0001g0250 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1828+4527C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13755165 | |||||||
| chr20:13755217 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1828+4475T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13755217 | |||||||
| chr20:13755236 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
289 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.1828+4456A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13755236 | |||||||
| chr20:13755419 | C | T | 33 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(30): Show |
33 | HG00423.hp1 HG00735.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1828+4273G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13755419 | |||||||
| chr20:13755583 | G | A | 95 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0218 others(92): Show |
101 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1828+4109C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13755583 | |||||||
| chr20:13755590 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1828+4102C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13755590 | |||||||
| chr20:13755986 | C | T | 33 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0111 others(30): Show |
39 | HG00741.hp2 HG01515.hp1 HG01517.hp2 others(36): Show |
intron_variant | MODIFIER | c.1828+3706G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13755986 | |||||||
| chr20:13756048 | G | T | 1 | a0001c0001t0001g0001 | 3 | HG01070.hp1 HG01071.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1828+3644C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13756048 | |||||||
| chr20:13756090 | T | C | 119 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0218 others(116): Show |
126 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.1828+3602A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13756090 | |||||||
| chr20:13756109 | G | A | 1 | a0002c0003t0001g0360 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1828+3583C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13756109 | |||||||
| chr20:13756299 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0031 |
2 | NA18982.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1828+3393T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13756299 | |||||||
| chr20:13756371 | A | G | 13 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0111 others(10): Show |
17 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1828+3321T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13756371 | |||||||
| chr20:13756531 | C | G | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1828+3161G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13756531 | |||||||
| chr20:13756580 | C | A | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1828+3112G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13756580 | |||||||
| chr20:13756741 | GTAAC | G | 7 | a0002c0003t0003g0134 a0002c0003t0003g0135 a0002c0003t0003g0136 others(4): Show |
7 | HG00280.hp1 HG00642.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1828+2947_1828+295 others(8): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13756741 | |||||||
| chr20:13756918 | T | C | 4 | a0003c0004t0002g0022 a0003c0004t0002g0332 a0003c0004t0002g0333 others(1): Show |
5 | HG00423.hp2 HG00597.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.1828+2774A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13756918 | |||||||
| chr20:13756963 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1828+2729C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13756963 | |||||||
| chr20:13756983 | AT | A | 7 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(4): Show |
9 | HG02257.hp2 HG02258.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1828+2708delA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13756983 | |||||||
| chr20:13757409 | T | A | 2 | a0001c0001t0001g0242 a0010c0020t0001g0131 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1828+2283A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13757409 | |||||||
| chr20:13757424 | G | A | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+2268C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13757424 | |||||||
| chr20:13757547 | T | C | 33 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0111 others(30): Show |
39 | HG00741.hp2 HG01515.hp1 HG01517.hp2 others(36): Show |
intron_variant | MODIFIER | c.1828+2145A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13757547 | |||||||
| chr20:13757594 | A | C | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1828+2098T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13757594 | |||||||
| chr20:13757661 | C | T | 2 | a0001c0002t0001g0268 a0001c0002t0001g0283 |
2 | HG01433.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1828+2031G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13757661 | |||||||
| chr20:13757691 | C | T | 4 | a0001c0002t0001g0269 a0001c0002t0001g0278 a0001c0002t0001g0279 others(1): Show |
4 | HG00741.hp1 HG01070.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1828+2001G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13757691 | |||||||
| chr20:13757751 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1828+1941C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13757751 | |||||||
| chr20:13758066 | GAC | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0056 others(2): Show |
7 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1828+1624_1828+162 others(6): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13758066 | |||||||
| chr20:13758070 | CAG | C | 266 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(263): Show |
282 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.1828+1620_1828+162 others(6): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13758070 | |||||||
| chr20:13758072 | G | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0056 others(2): Show |
7 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1828+1620C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13758072 | |||||||
| chr20:13758115 | C | A | 19 | a0003c0004t0002g0022 a0003c0004t0002g0128 a0003c0004t0002g0224 others(16): Show |
20 | HG00423.hp2 HG00597.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1828+1577G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13758115 | |||||||
| chr20:13758151 | T | C | 13 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0111 others(10): Show |
17 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1828+1541A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13758151 | |||||||
| chr20:13758219 | AG | A | 4 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | NA18747.hp1 NA18950.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1828+1472delC | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13758219 | |||||||
| chr20:13758244 | T | C | 1 | a0001c0002t0001g0277 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1828+1448A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13758244 | |||||||
| chr20:13758403 | T | C | 44 | a0001c0002t0001g0211 a0002c0003t0001g0012 a0002c0003t0001g0013 others(41): Show |
46 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1828+1289A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13758403 | |||||||
| chr20:13758538 | T | A | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1828+1154A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13758538 | |||||||
| chr20:13758649 | G | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
288 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.1828+1043C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13758649 | |||||||
| chr20:13758680 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1828+1012G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13758680 | |||||||
| chr20:13758710 | C | T | 2 | a0002c0003t0001g0151 a0002c0003t0001g0152 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1828+982G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13758710 | |||||||
| chr20:13758732 | G | A | 10 | a0001c0001t0001g0223 a0001c0001t0001g0319 a0001c0001t0001g0320 others(7): Show |
10 | HG01928.hp2 HG01934.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.1828+960C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13758732 | |||||||
| chr20:13758897 | A | C | 1 | a0003c0004t0002g0334 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1828+795T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13758897 | |||||||
| chr20:13759054 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
94 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1828+638T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13759054 | |||||||
| chr20:13759110 | C | T | 9 | a0001c0001t0001g0347 a0001c0001t0002g0095 a0001c0001t0002g0096 others(6): Show |
9 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1828+582G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13759110 | |||||||
| chr20:13759170 | T | G | 1 | a0001c0002t0001g0204 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1828+522A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13759170 | |||||||
| chr20:13759176 | A | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0285 |
2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1828+516T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13759176 | |||||||
| chr20:13759199 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1828+493C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13759199 | |||||||
| chr20:13759249 | A | G | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1828+443T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13759249 | |||||||
| chr20:13759267 | G | A | 2 | a0002c0003t0001g0141 a0002c0003t0001g0142 |
2 | HG00140.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1828+425C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13759267 | |||||||
| chr20:13759470 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1828+222G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13759470 | |||||||
| chr20:13759497 | T | C | 1 | a0004c0006t0001g0227 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1828+195A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13759497 | |||||||
| chr20:13759636 | G | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
159 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1828+56C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13759636 | |||||||
| chr20:13759640 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0054 a0001c0001t0001g0055 |
3 | NA18977.hp1 NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1828+52G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 9/13 | chr20 | 13759640 | |||||||
| chr20:13759919 | T | C | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1667-66A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13759919 | |||||||
| chr20:13759985 | T | A | 13 | a0003c0004t0002g0128 a0003c0004t0002g0224 a0003c0004t0002g0286 others(10): Show |
13 | HG00733.hp1 HG00735.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1667-132A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13759985 | |||||||
| chr20:13760060 | T | C | 7 | a0001c0001t0001g0223 a0001c0001t0001g0321 a0001c0001t0001g0322 others(4): Show |
7 | HG01928.hp2 HG01934.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1667-207A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760060 | |||||||
| chr20:13760180 | C | G | 304 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(301): Show |
328 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.1667-327G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760180 | |||||||
| chr20:13760207 | T | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG02572.hp2 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1667-354A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760207 | |||||||
| chr20:13760211 | C | T | 6 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
7 | HG02258.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1667-358G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760211 | |||||||
| chr20:13760259 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1667-406A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760259 | |||||||
| chr20:13760274 | G | A | 6 | a0001c0001t0002g0239 a0001c0001t0004g0010 a0001c0001t0004g0124 others(3): Show |
7 | HG02258.hp2 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1667-421C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760274 | |||||||
| chr20:13760281 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1667-428G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760281 | |||||||
| chr20:13760324 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1667-471C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760324 | |||||||
| chr20:13760364 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1667-511C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760364 | |||||||
| chr20:13760367 | C | T | 61 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0221 others(58): Show |
64 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1667-514G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760367 | |||||||
| chr20:13760375 | G | A | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1667-522C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760375 | |||||||
| chr20:13760406 | C | T | 2 | a0001c0001t0002g0097 a0001c0001t0002g0098 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1667-553G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760406 | |||||||
| chr20:13760419 | G | A | 347 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(344): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(370): Show |
intron_variant | MODIFIER | c.1667-566C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760419 | |||||||
| chr20:13760432 | C | T | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1667-579G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760432 | |||||||
| chr20:13760477 | C | T | 13 | a0001c0005t0001g0002 a0001c0005t0001g0249 a0001c0005t0001g0250 others(10): Show |
15 | HG00408.hp2 HG01496.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.1667-624G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760477 | |||||||
| chr20:13760479 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1667-626G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760479 | |||||||
| chr20:13760480 | G | A | 2 | a0002c0003t0003g0134 a0009c0018t0003g0138 |
2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1667-627C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760480 | |||||||
| chr20:13760486 | C | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0073 others(2): Show |
6 | HG00544.hp2 HG02523.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1667-633G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760486 | |||||||
| chr20:13760524 | ACCCCGTC others(33): Show |
A | 1 | a0002c0003t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1667-711_1667-672d others(42): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760524 | |||||||
| chr20:13760528 | C | G | 1 | a0001c0001t0001g0240 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1667-675G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760528 | |||||||
| chr20:13760529 | G | A | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1667-676C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760529 | |||||||
| chr20:13760557 | G | A | 2 | a0001c0005t0001g0002 a0001c0005t0001g0255 |
2 | HG02155.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1667-704C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760557 | |||||||
| chr20:13760557 | G | C | 1 | a0001c0001t0001g0073 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1667-704C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760557 | |||||||
| chr20:13760569 | A | G | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0052 others(1): Show |
4 | HG02027.hp2 NA18942.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.1667-716T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760569 | |||||||
| chr20:13760586 | C | T | 1 | a0001c0002t0001g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1667-733G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760586 | |||||||
| chr20:13760631 | C | G | 2 | a0002c0003t0001g0141 a0002c0003t0001g0142 |
2 | HG00140.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1667-778G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760631 | |||||||
| chr20:13760644 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1667-791C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760644 | |||||||
| chr20:13760652 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1667-799G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760652 | |||||||
| chr20:13760690 | C | T | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1667-837G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760690 | |||||||
| chr20:13760776 | C | T | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1667-923G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760776 | |||||||
| chr20:13760807 | T | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(344): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(370): Show |
intron_variant | MODIFIER | c.1667-954A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760807 | |||||||
| chr20:13760818 | G | A | 1 | a0003c0004t0002g0022 | 2 | HG02027.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1667-965C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760818 | |||||||
| chr20:13760822 | G | A | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1667-969C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760822 | |||||||
| chr20:13760867 | C | T | 1 | a0002c0003t0003g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1667-1014G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760867 | |||||||
| chr20:13760921 | G | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0363 |
2 | NA18960.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1667-1068C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760921 | |||||||
| chr20:13760940 | G | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(276): Show |
301 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1667-1087C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760940 | |||||||
| chr20:13760967 | A | C | 2 | a0001c0001t0002g0095 a0001c0001t0002g0102 |
2 | HG00741.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1667-1114T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13760967 | |||||||
| chr20:13761076 | C | T | 2 | a0002c0003t0001g0141 a0002c0003t0001g0142 |
2 | HG00140.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1667-1223G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761076 | |||||||
| chr20:13761123 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1667-1270C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761123 | |||||||
| chr20:13761142 | C | A | 5 | a0001c0002t0001g0266 a0001c0002t0001g0267 a0001c0002t0001g0288 others(2): Show |
5 | HG01255.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1667-1289G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761142 | |||||||
| chr20:13761147 | T | C | 358 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(355): Show |
384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.1667-1294A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761147 | |||||||
| chr20:13761224 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1667-1371G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761224 | |||||||
| chr20:13761282 | T | C | 25 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(22): Show |
27 | HG00741.hp2 HG01515.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.1667-1429A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761282 | |||||||
| chr20:13761353 | C | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1667-1500G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761353 | |||||||
| chr20:13761354 | G | A | 1 | a0001c0002t0001g0205 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1667-1501C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761354 | |||||||
| chr20:13761413 | TA | T | 124 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0033 others(121): Show |
134 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1667-1561delT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761413 | |||||||
| chr20:13761571 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1667-1718T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761571 | |||||||
| chr20:13761661 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0079 |
3 | HG02109.hp2 HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1667-1808T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761661 | |||||||
| chr20:13761764 | T | G | 304 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(301): Show |
328 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.1667-1911A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761764 | |||||||
| chr20:13761915 | T | C | 4 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
4 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1667-2062A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761915 | |||||||
| chr20:13761919 | G | T | 1 | a0010c0020t0001g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1667-2066C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761919 | |||||||
| chr20:13761966 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1667-2113A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761966 | |||||||
| chr20:13761996 | T | C | 1 | a0001c0002t0001g0345 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1667-2143A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13761996 | |||||||
| chr20:13762134 | A | G | 1 | a0001c0005t0001g0253 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1667-2281T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762134 | |||||||
| chr20:13762234 | A | C | 1 | a0001c0001t0001g0029 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1667-2381T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762234 | |||||||
| chr20:13762288 | C | T | 1 | a0002c0003t0001g0146 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1667-2435G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762288 | |||||||
| chr20:13762326 | A | G | 1 | a0001c0001t0001g0347 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1667-2473T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762326 | |||||||
| chr20:13762333 | A | C | 1 | a0004c0006t0001g0228 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1667-2480T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762333 | |||||||
| chr20:13762348 | C | A | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1667-2495G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762348 | |||||||
| chr20:13762393 | T | C | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1667-2540A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762393 | |||||||
| chr20:13762594 | G | A | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1667-2741C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762594 | |||||||
| chr20:13762626 | T | C | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1667-2773A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762626 | |||||||
| chr20:13762651 | A | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(276): Show |
301 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1667-2798T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762651 | |||||||
| chr20:13762770 | T | C | 25 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(22): Show |
27 | HG00741.hp2 HG01515.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.1667-2917A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762770 | |||||||
| chr20:13762854 | G | GT | 56 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(53): Show |
57 | HG00597.hp2 HG00621.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1667-3002dupA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762854 | |||||||
| chr20:13762854 | G | GTT | 50 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(47): Show |
53 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.1667-3003_1667-300 others(6): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762854 | |||||||
| chr20:13762854 | GT | G | 15 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0077 others(12): Show |
15 | HG01515.hp1 HG01517.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.1667-3002delA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762854 | |||||||
| chr20:13762867 | T | G | 1 | a0004c0006t0001g0236 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1667-3014A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762867 | |||||||
| chr20:13762886 | A | G | 7 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
8 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1667-3033T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762886 | |||||||
| chr20:13762901 | C | T | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1667-3048G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762901 | |||||||
| chr20:13762930 | G | A | 3 | a0002c0003t0003g0136 a0002c0003t0003g0357 a0002c0003t0003g0358 |
3 | HG00642.hp2 HG02257.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1667-3077C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762930 | |||||||
| chr20:13762954 | G | T | 25 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(22): Show |
27 | HG00741.hp2 HG01515.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.1667-3101C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762954 | |||||||
| chr20:13762983 | C | T | 1 | a0003c0004t0002g0332 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1667-3130G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762983 | |||||||
| chr20:13762996 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1667-3143C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13762996 | |||||||
| chr20:13763010 | G | A | 1 | a0002c0003t0001g0159 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1667-3157C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13763010 | |||||||
| chr20:13763020 | C | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(275): Show |
300 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.1667-3167G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13763020 | |||||||
| chr20:13763022 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1667-3169C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13763022 | |||||||
| chr20:13763236 | G | A | 3 | a0001c0001t0001g0263 a0001c0001t0004g0010 a0001c0001t0004g0126 |
4 | HG02818.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1667-3383C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13763236 | |||||||
| chr20:13763373 | C | T | 33 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(30): Show |
35 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1666+3404G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13763373 | |||||||
| chr20:13763406 | CA | C | 355 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(352): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.1666+3370delT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13763406 | |||||||
| chr20:13763498 | A | T | 1 | a0003c0004t0002g0022 | 2 | HG02027.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1666+3279T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13763498 | |||||||
| chr20:13763500 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1666+3277A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13763500 | |||||||
| chr20:13763661 | A | C | 4 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1666+3116T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13763661 | |||||||
| chr20:13763663 | A | T | 2 | a0001c0001t0001g0048 a0001c0001t0010g0087 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1666+3114T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13763663 | |||||||
| chr20:13763694 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1666+3083G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13763694 | |||||||
| chr20:13763704 | T | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0079 a0001c0001t0001g0106 |
4 | HG02109.hp2 HG02280.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1666+3073A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13763704 | |||||||
| chr20:13763907 | G | C | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1666+2870C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13763907 | |||||||
| chr20:13764004 | T | A | 1 | a0001c0001t0001g0009 | 2 | HG02148.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1666+2773A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13764004 | |||||||
| chr20:13764204 | T | C | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1666+2573A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13764204 | |||||||
| chr20:13764483 | G | C | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1666+2294C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13764483 | |||||||
| chr20:13764766 | TGAG | T | 3 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 |
3 | HG02559.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1666+2008_1666+201 others(7): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13764766 | |||||||
| chr20:13764843 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1666+1934G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13764843 | |||||||
| chr20:13764917 | TA | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
92 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1666+1859delT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13764917 | |||||||
| chr20:13764925 | A | C | 2 | a0001c0001t0001g0242 a0011c0011t0002g0241 |
2 | HG02717.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1666+1852T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13764925 | |||||||
| chr20:13764930 | A | C | 107 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0047 others(104): Show |
117 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1666+1847T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13764930 | |||||||
| chr20:13765099 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1666+1678G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13765099 | |||||||
| chr20:13765100 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1666+1677C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13765100 | |||||||
| chr20:13765258 | A | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(277): Show |
302 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.1666+1519T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13765258 | |||||||
| chr20:13765365 | A | G | 5 | a0001c0002t0001g0172 a0001c0002t0001g0175 a0001c0002t0001g0176 others(2): Show |
5 | NA18959.hp1 NA18967.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.1666+1412T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13765365 | |||||||
| chr20:13765388 | G | A | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1666+1389C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13765388 | |||||||
| chr20:13765728 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1666+1049T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13765728 | |||||||
| chr20:13765761 | A | C | 1 | a0002c0003t0003g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1666+1016T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13765761 | |||||||
| chr20:13765964 | T | C | 1 | a0002c0003t0001g0160 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1666+813A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13765964 | |||||||
| chr20:13766145 | T | C | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1666+632A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13766145 | |||||||
| chr20:13766151 | C | T | 1 | a0002c0003t0001g0244 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1666+626G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13766151 | |||||||
| chr20:13766540 | A | C | 4 | a0001c0002t0001g0175 a0001c0002t0001g0176 a0001c0002t0001g0207 others(1): Show |
4 | NA18959.hp1 NA18992.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.1666+237T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13766540 | |||||||
| chr20:13766571 | C | T | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1666+206G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13766571 | |||||||
| chr20:13766640 | T | A | 19 | a0003c0004t0002g0022 a0003c0004t0002g0128 a0003c0004t0002g0224 others(16): Show |
20 | HG00423.hp2 HG00597.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1666+137A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13766640 | |||||||
| chr20:13766641 | A | T | 1 | a0001c0002t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1666+136T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13766641 | |||||||
| chr20:13766689 | G | A | 2 | a0001c0001t0001g0242 a0010c0020t0001g0131 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1666+88C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 8/13 | chr20 | 13766689 | |||||||
| chr20:13767019 | A | T | 1 | a0001c0002t0001g0266 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1519-95T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13767019 | |||||||
| chr20:13767042 | T | A | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1519-118A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13767042 | |||||||
| chr20:13767268 | T | C | 1 | a0013c0014t0001g0364 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1519-344A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13767268 | |||||||
| chr20:13767394 | G | C | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1519-470C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13767394 | |||||||
| chr20:13767528 | T | G | 1 | a0007c0015t0001g0081 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1519-604A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13767528 | |||||||
| chr20:13767529 | C | CA | 9 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(6): Show |
9 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1519-606dupT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13767529 | |||||||
| chr20:13767678 | G | A | 1 | a0001c0001t0006g0003 | 3 | HG03195.hp2 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1519-754C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13767678 | |||||||
| chr20:13767723 | C | A | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1519-799G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13767723 | |||||||
| chr20:13767968 | A | C | 355 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(352): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.1519-1044T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13767968 | |||||||
| chr20:13768156 | A | C | 1 | a0002c0003t0001g0170 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1519-1232T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768156 | |||||||
| chr20:13768160 | A | G | 1 | a0002c0003t0001g0170 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1519-1236T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768160 | |||||||
| chr20:13768161 | A | C | 1 | a0002c0003t0001g0170 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1519-1237T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768161 | |||||||
| chr20:13768181 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
237 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.1519-1257G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768181 | |||||||
| chr20:13768195 | G | A | 286 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(283): Show |
309 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(306): Show |
intron_variant | MODIFIER | c.1519-1271C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768195 | |||||||
| chr20:13768227 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1519-1303G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768227 | |||||||
| chr20:13768290 | G | A | 25 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(22): Show |
27 | HG00741.hp2 HG01515.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.1519-1366C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768290 | |||||||
| chr20:13768387 | G | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
237 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.1519-1463C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768387 | |||||||
| chr20:13768560 | C | T | 1 | a0009c0018t0003g0138 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1518+1347G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768560 | |||||||
| chr20:13768591 | C | CA | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
103 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1518+1315dupT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768591 | |||||||
| chr20:13768816 | G | T | 5 | a0001c0001t0001g0220 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
5 | NA18960.hp1 NA18975.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.1518+1091C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768816 | |||||||
| chr20:13768840 | T | C | 2 | a0002c0003t0001g0161 a0002c0003t0001g0162 |
2 | HG00621.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1518+1067A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768840 | |||||||
| chr20:13768853 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0260 |
3 | HG00140.hp1 HG00323.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1518+1054G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768853 | |||||||
| chr20:13768854 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1518+1053C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768854 | |||||||
| chr20:13768875 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1518+1032G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768875 | |||||||
| chr20:13768897 | C | CA | 69 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(66): Show |
70 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1518+1009dupT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768897 | |||||||
| chr20:13768897 | C | CAA | 20 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(17): Show |
22 | HG00323.hp2 HG01081.hp1 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.1518+1008_1518+100 others(6): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768897 | |||||||
| chr20:13768897 | C | CAAA | 12 | a0001c0001t0001g0115 a0001c0001t0002g0095 a0001c0001t0002g0096 others(9): Show |
13 | HG00741.hp2 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1518+1007_1518+100 others(7): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768897 | |||||||
| chr20:13768913 | AG | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0089 a0001c0001t0001g0291 others(4): Show |
7 | HG00741.hp1 HG02451.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1518+993delC | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768913 | |||||||
| chr20:13768914 | G | A | 348 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(345): Show |
374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.1518+993C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768914 | |||||||
| chr20:13768959 | T | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
237 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.1518+948A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13768959 | |||||||
| chr20:13769171 | T | G | 1 | a0002c0003t0003g0135 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1518+736A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13769171 | |||||||
| chr20:13769232 | C | T | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1518+675G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13769232 | |||||||
| chr20:13769236 | G | A | 2 | a0001c0005t0001g0258 a0001c0005t0001g0259 |
2 | NA18965.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1518+671C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13769236 | |||||||
| chr20:13769386 | A | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0040 a0001c0001t0001g0044 others(4): Show |
8 | HG03654.hp2 NA18946.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.1518+521T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13769386 | |||||||
| chr20:13769604 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
264 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(261): Show |
intron_variant | MODIFIER | c.1518+303T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13769604 | |||||||
| chr20:13769640 | G | A | 1 | a0009c0018t0003g0138 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1518+267C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13769640 | |||||||
| chr20:13769801 | C | G | 1 | a0002c0003t0001g0145 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1518+106G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13769801 | |||||||
| chr20:13769832 | T | C | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1518+75A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13769832 | |||||||
| chr20:13769836 | ATAAG | A | 23 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0115 others(20): Show |
25 | HG00741.hp2 HG01515.hp1 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.1518+67_1518+70del others(4): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13769836 | |||||||
| chr20:13769854 | C | G | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1518+53G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13769854 | |||||||
| chr20:13769854 | CT | C | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1518+52delA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 7/13 | chr20 | 13769854 | |||||||
| chr20:13770180 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1404-159C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 6/13 | chr20 | 13770180 | |||||||
| chr20:13770225 | T | C | 1 | a0001c0001t0001g0034 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1404-204A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 6/13 | chr20 | 13770225 | |||||||
| chr20:13770318 | T | C | 1 | a0001c0002t0001g0214 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1404-297A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 6/13 | chr20 | 13770318 | |||||||
| chr20:13770426 | T | C | 3 | a0001c0002t0001g0229 a0004c0006t0001g0230 a0004c0006t0001g0231 |
3 | HG02165.hp1 HG02523.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1404-405A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 6/13 | chr20 | 13770426 | |||||||
| chr20:13770446 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1404-425C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 6/13 | chr20 | 13770446 | |||||||
| chr20:13770488 | G | C | 1 | a0001c0001t0004g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1404-467C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 6/13 | chr20 | 13770488 | |||||||
| chr20:13770490 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1404-469C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 6/13 | chr20 | 13770490 | |||||||
| chr20:13770518 | T | G | 1 | a0001c0001t0001g0325 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1404-497A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 6/13 | chr20 | 13770518 | |||||||
| chr20:13770551 | T | C | 1 | a0001c0002t0001g0208 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1404-530A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 6/13 | chr20 | 13770551 | |||||||
| chr20:13770835 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1403+496C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 6/13 | chr20 | 13770835 | |||||||
| chr20:13771859 | A | G | 1 | a0001c0001t0001g0346 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1251-376T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 5/13 | chr20 | 13771859 | |||||||
| chr20:13771912 | CT | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(277): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.1251-430delA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 5/13 | chr20 | 13771912 | |||||||
| chr20:13771912 | CTT | C | 50 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(47): Show |
54 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1251-431_1251-430d others(4): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 5/13 | chr20 | 13771912 | |||||||
| chr20:13772010 | A | T | 12 | a0002c0003t0001g0012 a0002c0003t0001g0143 a0002c0003t0001g0144 others(9): Show |
13 | HG00544.hp1 HG02165.hp2 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.1250+505T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 5/13 | chr20 | 13772010 | |||||||
| chr20:13772096 | T | TA | 9 | a0001c0001t0001g0093 a0001c0001t0002g0095 a0001c0001t0002g0096 others(6): Show |
9 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1250+418dupT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 5/13 | chr20 | 13772096 | |||||||
| chr20:13772097 | A | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1250+418T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 5/13 | chr20 | 13772097 | |||||||
| chr20:13772172 | A | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | HG02809.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1250+343T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 5/13 | chr20 | 13772172 | |||||||
| chr20:13772478 | A | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
99 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1250+37T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 5/13 | chr20 | 13772478 | |||||||
| chr20:13772819 | G | T | 1 | a0001c0002t0001g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1150-204C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13772819 | |||||||
| chr20:13772824 | G | A | 96 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0209 others(93): Show |
106 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1150-209C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13772824 | |||||||
| chr20:13773092 | G | C | 1 | a0001c0001t0001g0318 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1150-477C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773092 | |||||||
| chr20:13773444 | C | T | 1 | a0001c0012t0001g0251 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1150-829G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773444 | |||||||
| chr20:13773447 | G | A | 4 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150-832C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773447 | |||||||
| chr20:13773554 | T | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(273): Show |
298 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.1150-939A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773554 | |||||||
| chr20:13773716 | G | C | 1 | a0002c0003t0003g0137 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1150-1101C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773716 | |||||||
| chr20:13773821 | C | T | 23 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0115 others(20): Show |
25 | HG00741.hp2 HG01515.hp1 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.1150-1206G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773821 | |||||||
| chr20:13773822 | G | A | 1 | a0001c0001t0006g0003 | 3 | HG03195.hp2 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1150-1207C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773822 | |||||||
| chr20:13773823 | C | T | 2 | a0002c0003t0001g0141 a0002c0003t0001g0142 |
2 | HG00140.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1150-1208G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773823 | |||||||
| chr20:13773870 | C | T | 1 | a0001c0001t0004g0010 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1150-1255G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773870 | |||||||
| chr20:13773877 | T | A | 1 | a0001c0001t0001g0209 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1150-1262A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773877 | |||||||
| chr20:13773885 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1150-1270C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773885 | |||||||
| chr20:13773914 | T | C | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1149+1243A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773914 | |||||||
| chr20:13773952 | G | A | 4 | a0003c0004t0002g0328 a0003c0004t0002g0329 a0003c0004t0002g0330 others(1): Show |
4 | HG02040.hp2 NA18988.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1149+1205C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773952 | |||||||
| chr20:13773968 | G | A | 33 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(30): Show |
33 | HG00423.hp1 HG00735.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1149+1189C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773968 | |||||||
| chr20:13773981 | G | C | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1149+1176C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13773981 | |||||||
| chr20:13774020 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1149+1137C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774020 | |||||||
| chr20:13774043 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1149+1114G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774043 | |||||||
| chr20:13774071 | G | A | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1149+1086C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774071 | |||||||
| chr20:13774094 | C | CA | 10 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(7): Show |
11 | HG02258.hp2 HG02486.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1149+1062dupT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774094 | |||||||
| chr20:13774097 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1149+1060T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774097 | |||||||
| chr20:13774211 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1149+946T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774211 | |||||||
| chr20:13774262 | C | CATCCCA | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1149+889_1149+894d others(8): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774262 | |||||||
| chr20:13774274 | C | A | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1149+883G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774274 | |||||||
| chr20:13774277 | A | ATCCAAAA others(3): Show |
345 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(342): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(367): Show |
intron_variant | MODIFIER | c.1149+879_1149+880i others(12): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774277 | |||||||
| chr20:13774277 | A | ATGC | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1149+879_1149+880i others(5): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774277 | |||||||
| chr20:13774321 | G | A | 2 | a0001c0001t0001g0346 a0001c0001t0001g0347 |
2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1149+836C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774321 | |||||||
| chr20:13774385 | G | A | 43 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0132 others(40): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1149+772C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774385 | |||||||
| chr20:13774550 | A | G | 3 | a0001c0005t0001g0249 a0001c0005t0001g0250 a0001c0005t0001g0348 |
3 | HG02040.hp1 NA18974.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1149+607T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774550 | |||||||
| chr20:13774557 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0108 |
2 | NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1149+600A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774557 | |||||||
| chr20:13774893 | A | G | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | HG02809.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1149+264T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774893 | |||||||
| chr20:13774926 | A | C | 1 | a0001c0002t0001g0213 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1149+231T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13774926 | |||||||
| chr20:13775082 | C | CA | 10 | a0001c0001t0001g0115 a0001c0001t0001g0285 a0001c0001t0002g0119 others(7): Show |
11 | HG02257.hp2 HG02486.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1149+74dupT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13775082 | |||||||
| chr20:13775082 | CA | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(275): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1149+74delT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13775082 | |||||||
| chr20:13775082 | CAA | C | 35 | a0001c0001t0001g0041 a0001c0001t0001g0220 a0001c0001t0001g0221 others(32): Show |
35 | HG00423.hp1 HG00735.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1149+73_1149+74del others(2): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 4/13 | chr20 | 13775082 | |||||||
| chr20:13775344 | A | G | 1 | a0001c0001t0001g0025 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1036-74T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 3/13 | chr20 | 13775344 | |||||||
| chr20:13775350 | T | C | 19 | a0003c0004t0002g0022 a0003c0004t0002g0128 a0003c0004t0002g0224 others(16): Show |
20 | HG00423.hp2 HG00597.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1036-80A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 3/13 | chr20 | 13775350 | |||||||
| chr20:13775401 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1036-131C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 3/13 | chr20 | 13775401 | |||||||
| chr20:13775443 | T | C | 3 | a0001c0002t0001g0211 a0003c0004t0002g0286 a0003c0004t0002g0287 |
3 | HG00280.hp2 HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1036-173A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 3/13 | chr20 | 13775443 | |||||||
| chr20:13775513 | A | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
99 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1036-243T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 3/13 | chr20 | 13775513 | |||||||
| chr20:13775532 | A | G | 3 | a0003c0004t0002g0328 a0003c0004t0002g0329 a0003c0004t0002g0330 |
3 | HG02040.hp2 NA18988.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1036-262T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 3/13 | chr20 | 13775532 | |||||||
| chr20:13775619 | C | G | 1 | a0001c0001t0001g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1035+254G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 3/13 | chr20 | 13775619 | |||||||
| chr20:13775735 | C | A | 2 | a0001c0001t0001g0346 a0001c0001t0001g0347 |
2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1035+138G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 3/13 | chr20 | 13775735 | |||||||
| chr20:13775869 | T | A | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp2 | splice_region_variant&intron_variant | LOW | c.1035+4A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 3/13 | chr20 | 13775869 | |||||||
| chr20:13776409 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.638-139C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13776409 | |||||||
| chr20:13776569 | C | T | 61 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0221 others(58): Show |
64 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.638-299G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13776569 | |||||||
| chr20:13776673 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.638-403G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13776673 | |||||||
| chr20:13776689 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.638-419A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13776689 | |||||||
| chr20:13776791 | G | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
4 | HG02258.hp1 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-521C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13776791 | |||||||
| chr20:13776970 | T | C | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-700A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13776970 | |||||||
| chr20:13777076 | TGAG | T | 4 | a0003c0004t0002g0328 a0003c0004t0002g0329 a0003c0004t0002g0330 others(1): Show |
4 | HG02040.hp2 NA18988.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-809_638-807del others(3): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777076 | |||||||
| chr20:13777122 | T | G | 1 | a0012c0016t0003g0356 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.638-852A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777122 | |||||||
| chr20:13777279 | G | A | 3 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0290 |
3 | HG01255.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.638-1009C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777279 | |||||||
| chr20:13777285 | T | C | 33 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(30): Show |
33 | HG00423.hp1 HG00735.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.638-1015A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777285 | |||||||
| chr20:13777296 | G | A | 61 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0221 others(58): Show |
64 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.638-1026C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777296 | |||||||
| chr20:13777389 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.638-1119A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777389 | |||||||
| chr20:13777415 | T | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(276): Show |
301 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.638-1145A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777415 | |||||||
| chr20:13777444 | G | A | 1 | a0002c0010t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.638-1174C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777444 | |||||||
| chr20:13777448 | C | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-1178G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777448 | |||||||
| chr20:13777578 | C | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(275): Show |
300 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.638-1308G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777578 | |||||||
| chr20:13777588 | A | G | 1 | a0001c0001t0005g0121 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.638-1318T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777588 | |||||||
| chr20:13777632 | G | T | 1 | a0013c0014t0001g0364 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.638-1362C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777632 | |||||||
| chr20:13777758 | G | A | 1 | a0001c0002t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.638-1488C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777758 | |||||||
| chr20:13777767 | T | C | 25 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(22): Show |
27 | HG00741.hp2 HG01515.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.638-1497A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777767 | |||||||
| chr20:13777774 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.638-1504G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777774 | |||||||
| chr20:13777805 | T | TG | 355 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(352): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.638-1536_638-1535i others(3): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777805 | |||||||
| chr20:13777819 | G | C | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-1549C>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777819 | |||||||
| chr20:13777894 | G | T | 2 | a0005c0009t0001g0361 a0005c0009t0001g0362 |
2 | NA18993.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.638-1624C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777894 | |||||||
| chr20:13777998 | C | G | 1 | a0002c0003t0003g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.638-1728G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13777998 | |||||||
| chr20:13778277 | G | T | 3 | a0002c0003t0001g0012 a0002c0003t0001g0143 a0002c0003t0001g0144 |
4 | NA18955.hp1 NA19007.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-2007C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13778277 | |||||||
| chr20:13778283 | A | C | 1 | a0001c0001t0009g0216 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.638-2013T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13778283 | |||||||
| chr20:13778347 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.638-2077T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13778347 | |||||||
| chr20:13778394 | C | T | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.638-2124G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13778394 | |||||||
| chr20:13778463 | A | AT | 345 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(342): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(368): Show |
intron_variant | MODIFIER | c.638-2194dupA | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13778463 | |||||||
| chr20:13778504 | C | G | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-2234G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13778504 | |||||||
| chr20:13778720 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.638-2450T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13778720 | |||||||
| chr20:13778746 | T | G | 23 | a0001c0001t0001g0223 a0001c0001t0001g0319 a0001c0001t0001g0320 others(20): Show |
25 | HG00408.hp2 HG01496.hp2 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.638-2476A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13778746 | |||||||
| chr20:13778768 | C | T | 6 | a0001c0001t0002g0239 a0001c0001t0004g0010 a0001c0001t0004g0124 others(3): Show |
7 | HG02258.hp2 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.638-2498G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13778768 | |||||||
| chr20:13779006 | A | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(278): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.638-2736T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13779006 | |||||||
| chr20:13779033 | G | A | 1 | a0002c0003t0001g0168 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.638-2763C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13779033 | |||||||
| chr20:13779218 | C | CA | 8 | a0001c0001t0001g0036 a0001c0001t0001g0115 a0001c0001t0001g0327 others(5): Show |
8 | HG01175.hp2 HG01928.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-2949dupT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13779218 | |||||||
| chr20:13779227 | A | C | 1 | a0002c0003t0001g0140 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.638-2957T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13779227 | |||||||
| chr20:13779228 | C | A | 4 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
4 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-2958G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13779228 | |||||||
| chr20:13779229 | C | A | 1 | a0002c0003t0001g0170 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.638-2959G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13779229 | |||||||
| chr20:13779316 | T | C | 7 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
8 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-3046A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13779316 | |||||||
| chr20:13779446 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.637+3058C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13779446 | |||||||
| chr20:13779645 | G | A | 2 | a0001c0007t0002g0017 a0001c0007t0002g0238 |
3 | HG02257.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.637+2859C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13779645 | |||||||
| chr20:13779725 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
4 | HG02258.hp1 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+2779C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13779725 | |||||||
| chr20:13779952 | C | G | 1 | a0002c0003t0001g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.637+2552G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13779952 | |||||||
| chr20:13780012 | G | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG02572.hp2 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+2492C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13780012 | |||||||
| chr20:13780091 | T | C | 1 | a0003c0004t0002g0344 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.637+2413A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13780091 | |||||||
| chr20:13780137 | G | A | 19 | a0003c0004t0002g0022 a0003c0004t0002g0128 a0003c0004t0002g0224 others(16): Show |
20 | HG00423.hp2 HG00597.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.637+2367C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13780137 | |||||||
| chr20:13780297 | T | G | 5 | a0004c0006t0001g0233 a0004c0006t0001g0234 a0004c0006t0001g0235 others(2): Show |
5 | NA18942.hp1 NA18954.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+2207A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13780297 | |||||||
| chr20:13780337 | T | G | 1 | a0013c0014t0001g0364 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.637+2167A>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13780337 | |||||||
| chr20:13780412 | C | T | 304 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(301): Show |
328 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.637+2092G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13780412 | |||||||
| chr20:13780524 | C | T | 1 | a0001c0002t0001g0172 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.637+1980G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13780524 | |||||||
| chr20:13780602 | GACCTCTT others(11): Show |
G | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+1884_637+1901d others(20): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13780602 | |||||||
| chr20:13780648 | G | GCTATCAA others(29): Show |
1 | a0001c0001t0001g0242 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.637+1820_637+1855d others(38): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13780648 | |||||||
| chr20:13780682 | G | A | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.637+1822C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13780682 | |||||||
| chr20:13780863 | A | G | 1 | a0001c0002t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.637+1641T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13780863 | |||||||
| chr20:13780968 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.637+1536G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13780968 | |||||||
| chr20:13781011 | C | T | 95 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0209 others(92): Show |
105 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.637+1493G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13781011 | |||||||
| chr20:13781270 | GA | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
6 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.637+1233delT | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13781270 | |||||||
| chr20:13781498 | T | C | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.637+1006A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13781498 | |||||||
| chr20:13781513 | C | T | 2 | a0001c0001t0005g0120 a0001c0001t0005g0121 |
2 | NA18970.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.637+991G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13781513 | |||||||
| chr20:13781582 | C | T | 1 | a0001c0002t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.637+922G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13781582 | |||||||
| chr20:13781586 | C | T | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+918G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13781586 | |||||||
| chr20:13781626 | G | T | 1 | a0010c0020t0001g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.637+878C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13781626 | |||||||
| chr20:13781681 | C | T | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+823G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13781681 | |||||||
| chr20:13781755 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.637+749C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13781755 | |||||||
| chr20:13781772 | C | T | 355 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(352): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.637+732G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13781772 | |||||||
| chr20:13782002 | G | A | 1 | a0001c0002t0001g0225 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.637+502C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13782002 | |||||||
| chr20:13782138 | A | G | 7 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
8 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+366T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13782138 | |||||||
| chr20:13782249 | T | C | 1 | a0001c0002t0001g0345 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.637+255A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13782249 | |||||||
| chr20:13782258 | T | A | 2 | a0001c0001t0001g0346 a0001c0001t0001g0347 |
2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.637+246A>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13782258 | |||||||
| chr20:13782278 | A | T | 8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+226T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 2/13 | chr20 | 13782278 | |||||||
| chr20:13783209 | T | C | 1 | a0001c0001t0002g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-43-26A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13783209 | |||||||
| chr20:13783250 | C | CATTA | 304 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(301): Show |
328 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.-43-68_-43-67insTA others(2): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13783250 | |||||||
| chr20:13783357 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
94 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-43-174T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13783357 | |||||||
| chr20:13783391 | C | G | 1 | a0001c0001t0001g0242 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-43-208G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13783391 | |||||||
| chr20:13783451 | G | A | 11 | a0001c0002t0001g0229 a0004c0006t0001g0227 a0004c0006t0001g0228 others(8): Show |
11 | HG00621.hp1 HG02165.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-43-268C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13783451 | |||||||
| chr20:13783466 | T | C | 1 | a0001c0005t0001g0348 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-43-283A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13783466 | |||||||
| chr20:13783579 | C | T | 1 | a0011c0011t0002g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-43-396G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13783579 | |||||||
| chr20:13783770 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-43-587G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13783770 | |||||||
| chr20:13783778 | C | T | 8 | a0002c0003t0003g0133 a0002c0003t0003g0134 a0002c0003t0003g0135 others(5): Show |
8 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-595G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13783778 | |||||||
| chr20:13783833 | A | T | 4 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-650T>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13783833 | |||||||
| chr20:13784008 | T | C | 355 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(352): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.-43-825A>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784008 | |||||||
| chr20:13784107 | A | G | 1 | a0002c0003t0001g0132 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-44+773T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784107 | |||||||
| chr20:13784283 | A | AC | 76 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(73): Show |
82 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.-44+596_-44+597ins others(1): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784283 | |||||||
| chr20:13784283 | A | ACC | 14 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(11): Show |
14 | HG02145.hp1 HG02572.hp2 HG02738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+596_-44+597ins others(2): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784283 | |||||||
| chr20:13784284 | A | AC | 120 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(117): Show |
130 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-44+595dupG | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784284 | |||||||
| chr20:13784284 | A | ACC | 116 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0218 others(113): Show |
121 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-44+594_-44+595dup others(2): Show |
ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784284 | |||||||
| chr20:13784284 | A | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
121 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.-44+596T>G | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784284 | |||||||
| chr20:13784469 | G | T | 1 | a0010c0020t0001g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-44+411C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784469 | |||||||
| chr20:13784522 | G | A | 1 | a0013c0014t0001g0364 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-44+358C>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784522 | |||||||
| chr20:13784634 | C | G | 3 | a0001c0002t0001g0011 a0001c0002t0001g0129 a0001c0002t0001g0130 |
4 | HG01255.hp2 HG01981.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+246G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784634 | |||||||
| chr20:13784662 | G | T | 1 | a0003c0004t0002g0128 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-44+218C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784662 | |||||||
| chr20:13784669 | G | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+211C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784669 | |||||||
| chr20:13784708 | G | T | 4 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0122 others(1): Show |
4 | HG03704.hp2 NA18970.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+172C>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784708 | |||||||
| chr20:13784713 | A | G | 4 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+167T>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784713 | |||||||
| chr20:13784845 | C | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | NA18952.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-44+35G>T | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784845 | |||||||
| chr20:13784845 | C | G | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(2): Show |
5 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+35G>C | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784845 | |||||||
| chr20:13784861 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
102 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.-44+19G>A | ESF1 | ENSG00000089048.15 | transcript | ENST00000617257.2 | protein_coding | 1/13 | chr20 | 13784861 |