Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6498 |
| ensemblid | ENSG00000136603.15 |
| hgncid | 10897 |
| symbol | SKIL |
| name | SKI like proto-oncogene |
| refseq_nuc | NM_005414.5 |
| refseq_prot | NP_005405.2 |
| ensembl_nuc | ENST00000259119.9 |
| ensembl_prot | ENSP00000259119.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 170357715 |
| end | 170396835 |
| strand | + |
| ver | v1.2 |
| region | chr3:170357715-170396835 |
| region5000 | chr3:170352715-170401835 |
| regionname0 | SKIL_chr3_170357715_170396835 |
| regionname5000 | SKIL_chr3_170352715_170401835 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 684 | 233 | 34 | 52 | 115 | 7 | 24 | 86 | SKIL_chr3_170352715_170401835 | SKIL | MENLQ others(679): Show |
chr3 | 170352715 | 170401835 |
| a0002 | 1/0 | 684 | 118 | 57 | 17 | 33 | 1 | 9 | 25 | SKIL_chr3_170352715_170401835 | SKIL | MENLQ others(679): Show |
chr3 | 170352715 | 170401835 |
| a0003 | 0/0 | 684 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | MENLQ others(679): Show |
chr3 | 170352715 | 170401835 |
| a0004 | 0/0 | 684 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SKIL_chr3_170352715_170401835 | SKIL | MENLQ others(679): Show |
chr3 | 170352715 | 170401835 |
| a0005 | 0/0 | 684 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SKIL_chr3_170352715_170401835 | SKIL | MENLQ others(679): Show |
chr3 | 170352715 | 170401835 |
| a0006 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | MENLQ others(679): Show |
chr3 | 170352715 | 170401835 |
| a0007 | 0/0 | 684 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | MENLQ others(679): Show |
chr3 | 170352715 | 170401835 |
| a0008 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | MENLQ others(679): Show |
chr3 | 170352715 | 170401835 |
| a0009 | 0/0 | 684 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | MENLQ others(679): Show |
chr3 | 170352715 | 170401835 |
| a0010 | 0/0 | 393 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | MENLQ others(388): Show |
chr3 | 170352715 | 170401835 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2052 | 221 | 34 | 52 | 103 | 7 | 24 | SKIL_chr3_170352715_170401835 | SKIL | ATGGA others(2047): Show |
chr3 | 170352715 | 170401835 | ||
| a0001c0003 | 0/0 | 2052 | 12 | 0 | 0 | 12 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ATGGA others(2047): Show |
chr3 | 170352715 | 170401835 | ||
| a0002c0002 | 1/0 | 2052 | 116 | 55 | 17 | 33 | 1 | 9 | SKIL_chr3_170352715_170401835 | SKIL | ATGGA others(2047): Show |
chr3 | 170352715 | 170401835 | ||
| a0002c0008 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ATGGA others(2047): Show |
chr3 | 170352715 | 170401835 | ||
| a0002c0009 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ATGGA others(2047): Show |
chr3 | 170352715 | 170401835 | ||
| a0003c0005 | 0/0 | 2052 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ATGGA others(2047): Show |
chr3 | 170352715 | 170401835 | ||
| a0004c0004 | 0/0 | 2052 | 2 | 0 | 0 | 0 | 0 | 2 | SKIL_chr3_170352715_170401835 | SKIL | ATGGA others(2047): Show |
chr3 | 170352715 | 170401835 | ||
| a0005c0006 | 0/0 | 2052 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ATGGA others(2047): Show |
chr3 | 170352715 | 170401835 | ||
| a0006c0011 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ATGGA others(2047): Show |
chr3 | 170352715 | 170401835 | ||
| a0007c0010 | 0/0 | 2052 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ATGGA others(2047): Show |
chr3 | 170352715 | 170401835 | ||
| a0008c0007 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ATGGA others(2047): Show |
chr3 | 170352715 | 170401835 | ||
| a0009c0013 | 0/0 | 2052 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ATGGA others(2047): Show |
chr3 | 170352715 | 170401835 | ||
| a0010c0012 | 0/0 | 2052 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ATGGA others(2047): Show |
chr3 | 170352715 | 170401835 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7150 | 61 | 12 | 8 | 33 | 1 | 7 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0002 | 0/0 | 7152 | 33 | 0 | 9 | 22 | 2 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7147): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0003 | 0/0 | 7149 | 21 | 0 | 13 | 3 | 2 | 3 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7144): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0004 | 0/0 | 7149 | 19 | 1 | 5 | 10 | 0 | 3 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7144): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0007 | 0/1 | 7150 | 12 | 0 | 4 | 7 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0008 | 0/0 | 7153 | 14 | 5 | 2 | 5 | 1 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7148): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0009 | 0/0 | 7151 | 8 | 2 | 0 | 5 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7146): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0012 | 0/0 | 7152 | 5 | 1 | 0 | 0 | 0 | 4 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7147): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0014 | 0/0 | 7151 | 4 | 0 | 1 | 3 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7146): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0016 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7144): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0021 | 0/0 | 7154 | 3 | 3 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7149): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0022 | 0/0 | 7151 | 3 | 3 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7146): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0023 | 0/0 | 7151 | 3 | 0 | 1 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7146): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0024 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7147): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0036 | 0/0 | 7151 | 2 | 0 | 1 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7146): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0037 | 0/0 | 7153 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7148): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0038 | 0/0 | 7155 | 2 | 0 | 1 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7150): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0039 | 0/0 | 7151 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7146): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0040 | 0/0 | 7150 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0060 | 0/0 | 7153 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7148): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0061 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7144): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0062 | 0/0 | 7149 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7144): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0063 | 0/0 | 7150 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0064 | 0/0 | 7150 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0065 | 0/0 | 7152 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7147): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0067 | 0/0 | 7151 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7146): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0068 | 0/0 | 7154 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7149): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0069 | 0/0 | 7152 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7147): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0070 | 0/0 | 7152 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7147): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0071 | 0/0 | 7153 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7148): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0072 | 0/0 | 7152 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7147): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0073 | 0/0 | 7152 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7147): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0074 | 0/0 | 7151 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7146): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0075 | 0/0 | 7148 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7143): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0077 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7144): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0078 | 0/0 | 7150 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0079 | 0/0 | 7150 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0083 | 0/0 | 7150 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0084 | 0/0 | 7151 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7146): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0085 | 0/0 | 7150 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0086 | 0/0 | 7151 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7146): Show |
chr3 | 170352715 | 170401835 |
| a0001c0001t0087 | 0/0 | 7153 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7148): Show |
chr3 | 170352715 | 170401835 |
| a0001c0003t0004 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7144): Show |
chr3 | 170352715 | 170401835 |
| a0001c0003t0007 | 0/0 | 7150 | 3 | 0 | 0 | 3 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0001c0003t0014 | 0/0 | 7151 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7146): Show |
chr3 | 170352715 | 170401835 |
| a0001c0003t0024 | 0/0 | 7152 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7147): Show |
chr3 | 170352715 | 170401835 |
| a0001c0003t0043 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7144): Show |
chr3 | 170352715 | 170401835 |
| a0001c0003t0076 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7144): Show |
chr3 | 170352715 | 170401835 |
| a0001c0003t0081 | 0/0 | 7151 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7146): Show |
chr3 | 170352715 | 170401835 |
| a0001c0003t0082 | 0/0 | 7154 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7149): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0002 | 0/0 | 7152 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7147): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0005 | 1/0 | 7155 | 19 | 3 | 7 | 3 | 0 | 5 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7150): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0006 | 0/0 | 7146 | 15 | 0 | 1 | 13 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7141): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0010 | 0/0 | 7156 | 8 | 2 | 2 | 3 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7151): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0011 | 0/0 | 7158 | 7 | 7 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7153): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0013 | 0/0 | 7154 | 6 | 5 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7149): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0015 | 0/0 | 7155 | 5 | 0 | 0 | 5 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7150): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0016 | 0/0 | 7149 | 4 | 3 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7144): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0017 | 0/0 | 7155 | 3 | 2 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7150): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0018 | 0/0 | 7147 | 3 | 0 | 1 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7142): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0019 | 0/0 | 7155 | 3 | 3 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7150): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0020 | 0/0 | 7156 | 3 | 3 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7151): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0025 | 0/0 | 7157 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7152): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0026 | 0/0 | 7157 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7152): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0027 | 0/0 | 7154 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7149): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0028 | 0/0 | 7155 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7150): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0029 | 0/0 | 7156 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7151): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0030 | 0/0 | 7156 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7151): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0031 | 0/0 | 7157 | 2 | 1 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7152): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0032 | 0/0 | 7158 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7153): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0033 | 0/0 | 7156 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7151): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0034 | 0/0 | 7157 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7152): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0035 | 0/0 | 7159 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7154): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0041 | 0/0 | 7153 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7148): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0042 | 0/0 | 7157 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7152): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0044 | 0/0 | 7145 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7140): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0045 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7141): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0046 | 0/0 | 7146 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7141): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0047 | 0/0 | 7145 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7140): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0049 | 0/0 | 7158 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7153): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0051 | 0/0 | 7157 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7152): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0052 | 0/0 | 7155 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7150): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0053 | 0/0 | 7157 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7152): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0054 | 0/0 | 7155 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7150): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0055 | 0/0 | 7157 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7152): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0056 | 0/0 | 7155 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7150): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0057 | 0/0 | 7150 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0058 | 0/0 | 7140 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7135): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0059 | 0/0 | 7140 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7135): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0088 | 0/0 | 7154 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7149): Show |
chr3 | 170352715 | 170401835 |
| a0002c0002t0089 | 0/0 | 7158 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7153): Show |
chr3 | 170352715 | 170401835 |
| a0002c0008t0050 | 0/0 | 7158 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7153): Show |
chr3 | 170352715 | 170401835 |
| a0002c0009t0032 | 0/0 | 7158 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7153): Show |
chr3 | 170352715 | 170401835 |
| a0003c0005t0012 | 0/0 | 7152 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7147): Show |
chr3 | 170352715 | 170401835 |
| a0004c0004t0004 | 0/0 | 7149 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7144): Show |
chr3 | 170352715 | 170401835 |
| a0004c0004t0080 | 0/0 | 7150 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0005c0006t0001 | 0/0 | 7150 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0006c0011t0001 | 0/0 | 7150 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0007c0010t0001 | 0/0 | 7150 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0008c0007t0048 | 0/0 | 7154 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7149): Show |
chr3 | 170352715 | 170401835 |
| a0009c0013t0066 | 0/0 | 7150 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7145): Show |
chr3 | 170352715 | 170401835 |
| a0010c0012t0009 | 0/0 | 7151 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | ACAGC others(7146): Show |
chr3 | 170352715 | 170401835 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0007g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0007g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0007g0080 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0007g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0008g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0008g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0008g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0008g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0008g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0008g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0009g0002 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0009g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0009g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0009g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0009g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0009g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0012g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0012g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0012g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0012g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0012g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0014g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0014g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0014g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0014g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0016g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0021g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0021g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0021g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0022g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0022g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0022g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0023g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0023g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0023g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0024g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0036g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0036g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0037g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0037g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0038g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0038g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0039g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0040g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0040g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0060g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0061g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0062g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0063g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0064g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0065g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0067g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0068g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0069g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0070g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0071g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0072g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0073g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0074g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0075g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0077g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0078g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0079g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0083g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0084g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0085g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0086g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0001t0087g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0003t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0003t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0003t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0003t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0003t0014g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0003t0014g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0003t0024g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0003t0024g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0003t0043g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0003t0076g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0003t0081g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0001c0003t0082g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0252 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0005g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0006g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0010g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0010g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0010g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0010g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0010g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0010g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0010g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0011g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0011g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0011g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0011g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0011g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0011g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0013g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0013g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0013g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0013g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0013g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0013g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0015g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0015g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0015g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0015g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0015g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0016g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0016g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0016g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0016g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0017g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0017g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0017g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0018g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0018g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0018g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0019g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0019g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0019g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0020g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0020g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0020g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0025g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0025g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0026g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0026g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0027g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0027g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0028g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0028g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0029g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0029g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0030g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0030g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0031g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0031g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0032g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0033g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0033g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0034g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0034g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0035g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0035g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0041g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0042g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0044g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0045g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0046g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0047g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0049g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0051g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0052g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0053g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0054g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0055g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0056g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0057g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0058g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0059g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0088g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0002t0089g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0008t0050g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0002c0009t0032g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0003c0005t0012g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0003c0005t0012g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0004c0004t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0004c0004t0080g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0005c0006t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0005c0006t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0006c0011t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0007c0010t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0008c0007t0048g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0009c0013t0066g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| a0010c0012t0009g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0011 | EUR | GBR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0112 | EUR | GBR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0157 | EUR | FIN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0107 | EUR | FIN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00323 | hp2 | a0001 | c0001 | t0075 | g0234 | EUR | FIN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00423 | hp1 | a0001 | c0001 | t0072 | g0086 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00423 | hp2 | a0001 | c0001 | t0084 | g0060 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00438 | hp2 | a0001 | c0003 | t0007 | g0077 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00558 | hp2 | a0002 | c0002 | t0006 | g0258 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00609 | hp2 | a0001 | c0001 | t0085 | g0001 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00621 | hp1 | a0006 | c0011 | t0001 | g0114 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00639 | hp1 | a0001 | c0001 | t0036 | g0104 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00673 | hp1 | a0001 | c0001 | t0008 | g0088 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00673 | hp2 | a0001 | c0001 | t0040 | g0055 | EAS | CHS | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00735 | hp1 | a0001 | c0001 | t0063 | g0165 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00735 | hp2 | a0001 | c0001 | t0073 | g0076 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0222 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0015 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01069 | hp1 | a0002 | c0002 | t0005 | g0017 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0081 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01070 | hp1 | a0001 | c0001 | t0038 | g0152 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01071 | hp1 | a0002 | c0002 | t0005 | g0256 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01081 | hp2 | a0002 | c0002 | t0005 | g0249 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01099 | hp1 | a0002 | c0002 | t0010 | g0017 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0237 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01106 | hp2 | a0002 | c0002 | t0005 | g0257 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01109 | hp1 | a0001 | c0001 | t0037 | g0072 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01109 | hp2 | a0001 | c0001 | t0037 | g0113 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01168 | hp2 | a0002 | c0002 | t0026 | g0305 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01169 | hp2 | a0002 | c0002 | t0026 | g0306 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01175 | hp1 | a0002 | c0002 | t0032 | g0253 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0226 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01243 | hp1 | a0007 | c0010 | t0001 | g0171 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01243 | hp2 | a0002 | c0002 | t0013 | g0272 | AMR | PUR | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01255 | hp2 | a0002 | c0002 | t0005 | g0330 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01256 | hp1 | a0001 | c0001 | t0023 | g0108 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01257 | hp2 | a0003 | c0005 | t0012 | g0071 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01258 | hp1 | a0003 | c0005 | t0012 | g0075 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01358 | hp1 | a0002 | c0002 | t0017 | g0303 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01358 | hp2 | a0001 | c0001 | t0070 | g0106 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01361 | hp1 | a0001 | c0001 | t0008 | g0090 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01361 | hp2 | a0002 | c0002 | t0010 | g0016 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01433 | hp2 | a0002 | c0002 | t0016 | g0026 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01496 | hp2 | a0002 | c0002 | t0005 | g0242 | AMR | CLM | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01884 | hp2 | a0002 | c0002 | t0034 | g0295 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0079 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01891 | hp2 | a0002 | c0002 | t0031 | g0003 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01928 | hp1 | a0001 | c0001 | t0008 | g0190 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01928 | hp2 | a0002 | c0002 | t0005 | g0255 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0233 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0087 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01952 | hp1 | a0001 | c0001 | t0014 | g0057 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01952 | hp2 | a0001 | c0001 | t0060 | g0194 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01978 | hp1 | a0002 | c0002 | t0018 | g0318 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0225 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02040 | hp1 | a0001 | c0003 | t0004 | g0084 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02055 | hp1 | a0002 | c0002 | t0013 | g0296 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02055 | hp2 | a0002 | c0002 | t0088 | g0309 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02056 | hp1 | a0002 | c0002 | t0029 | g0260 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02071 | hp1 | a0002 | c0002 | t0005 | g0245 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02071 | hp2 | a0002 | c0002 | t0018 | g0314 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02074 | hp1 | a0001 | c0001 | t0008 | g0095 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02074 | hp2 | a0002 | c0002 | t0010 | g0248 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02080 | hp1 | a0001 | c0001 | t0007 | g0224 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02080 | hp2 | a0002 | c0002 | t0029 | g0264 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02135 | hp1 | a0001 | c0001 | t0007 | g0006 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02135 | hp2 | a0002 | c0002 | t0005 | g0213 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02145 | hp1 | a0002 | c0002 | t0053 | g0282 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0059 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CDX | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CDX | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CDX | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CDX | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02257 | hp1 | a0002 | c0002 | t0020 | g0283 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02257 | hp2 | a0001 | c0001 | t0074 | g0007 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02258 | hp1 | a0001 | c0001 | t0067 | g0139 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02258 | hp2 | a0002 | c0002 | t0011 | g0273 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02273 | hp2 | a0001 | c0001 | t0065 | g0094 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0002 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02280 | hp2 | a0001 | c0001 | t0012 | g0050 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02293 | hp2 | a0002 | c0002 | t0006 | g0326 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02451 | hp1 | a0002 | c0002 | t0041 | g0331 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02451 | hp2 | a0002 | c0002 | t0011 | g0269 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0063 | EAS | KHV | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02572 | hp1 | a0002 | c0002 | t0013 | g0274 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02572 | hp2 | a0002 | c0002 | t0020 | g0278 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02615 | hp1 | a0002 | c0002 | t0034 | g0018 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02622 | hp1 | a0002 | c0002 | t0058 | g0027 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02622 | hp2 | a0002 | c0002 | t0035 | g0004 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02630 | hp1 | a0002 | c0002 | t0027 | g0298 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02630 | hp2 | a0002 | c0002 | t0010 | g0292 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0051 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02647 | hp2 | a0002 | c0002 | t0005 | g0288 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02698 | hp1 | a0001 | c0001 | t0086 | g0034 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02698 | hp2 | a0001 | c0001 | t0036 | g0038 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02717 | hp1 | a0002 | c0002 | t0019 | g0212 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0037 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02723 | hp1 | a0002 | c0002 | t0059 | g0028 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02723 | hp2 | a0001 | c0001 | t0021 | g0041 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02738 | hp1 | a0004 | c0004 | t0080 | g0227 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02809 | hp1 | a0002 | c0002 | t0016 | g0022 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02809 | hp2 | a0002 | c0002 | t0011 | g0268 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02818 | hp1 | a0002 | c0002 | t0054 | g0294 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02818 | hp2 | a0002 | c0002 | t0016 | g0025 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02886 | hp1 | a0002 | c0002 | t0035 | g0018 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02886 | hp2 | a0002 | c0002 | t0005 | g0289 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02896 | hp1 | a0002 | c0002 | t0005 | g0290 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02896 | hp2 | a0002 | c0002 | t0025 | g0302 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02897 | hp2 | a0002 | c0002 | t0017 | g0299 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02922 | hp1 | a0002 | c0002 | t0011 | g0271 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02922 | hp2 | a0002 | c0002 | t0051 | g0334 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02965 | hp1 | a0001 | c0001 | t0087 | g0065 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02965 | hp2 | a0002 | c0002 | t0033 | g0293 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02970 | hp1 | a0002 | c0009 | t0032 | g0286 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02976 | hp1 | a0002 | c0008 | t0050 | g0019 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02976 | hp2 | a0002 | c0002 | t0011 | g0267 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03041 | hp1 | a0001 | c0001 | t0022 | g0042 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03041 | hp2 | a0008 | c0007 | t0048 | g0310 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03098 | hp1 | a0002 | c0002 | t0055 | g0291 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03098 | hp2 | a0001 | c0001 | t0022 | g0078 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03139 | hp1 | a0002 | c0002 | t0011 | g0004 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03139 | hp2 | a0001 | c0001 | t0071 | g0040 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03209 | hp1 | a0001 | c0001 | t0068 | g0196 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03209 | hp2 | a0002 | c0002 | t0030 | g0285 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03225 | hp1 | a0002 | c0002 | t0020 | g0277 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03239 | hp2 | a0002 | c0002 | t0056 | g0244 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03453 | hp1 | a0002 | c0002 | t0011 | g0004 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03453 | hp2 | a0002 | c0002 | t0049 | g0019 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03486 | hp1 | a0002 | c0002 | t0027 | g0307 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03486 | hp2 | a0002 | c0002 | t0033 | g0332 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03490 | hp1 | a0001 | c0001 | t0012 | g0049 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03491 | hp1 | a0001 | c0001 | t0062 | g0151 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03491 | hp2 | a0002 | c0002 | t0005 | g0241 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03492 | hp1 | a0002 | c0002 | t0005 | g0003 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03492 | hp2 | a0001 | c0001 | t0012 | g0070 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03516 | hp1 | a0002 | c0002 | t0057 | g0023 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | ESN | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0054 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03540 | hp2 | a0002 | c0002 | t0013 | g0270 | AFR | GWD | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03579 | hp1 | a0002 | c0002 | t0013 | g0297 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03654 | hp2 | a0002 | c0002 | t0005 | g0003 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03669 | hp2 | a0001 | c0001 | t0083 | g0035 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03688 | hp1 | a0001 | c0001 | t0012 | g0073 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03704 | hp1 | a0001 | c0001 | t0009 | g0180 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0230 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03710 | hp1 | a0001 | c0001 | t0008 | g0182 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03710 | hp2 | a0002 | c0002 | t0010 | g0016 | SAS | PJL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03831 | hp1 | a0002 | c0002 | t0006 | g0315 | SAS | BEB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03831 | hp2 | a0009 | c0013 | t0066 | g0136 | SAS | BEB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03834 | hp1 | a0002 | c0002 | t0005 | g0251 | SAS | BEB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0239 | SAS | BEB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0178 | SAS | BEB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG04115 | hp1 | a0004 | c0004 | t0004 | g0223 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG04204 | hp1 | a0002 | c0002 | t0031 | g0250 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG04204 | hp2 | a0001 | c0001 | t0012 | g0074 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0231 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG04228 | hp2 | a0001 | c0001 | t0038 | g0141 | SAS | STU | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18522 | hp1 | a0002 | c0002 | t0025 | g0301 | AFR | YRI | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18522 | hp2 | a0002 | c0002 | t0019 | g0276 | AFR | YRI | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18612 | hp1 | a0002 | c0002 | t0010 | g0246 | EAS | CHB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CHB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | CHB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | CHB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18939 | hp1 | a0001 | c0001 | t0039 | g0012 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18939 | hp2 | a0002 | c0002 | t0015 | g0263 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18942 | hp1 | a0001 | c0001 | t0024 | g0217 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18942 | hp2 | a0001 | c0003 | t0024 | g0046 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18948 | hp1 | a0001 | c0001 | t0077 | g0221 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18949 | hp2 | a0002 | c0002 | t0006 | g0325 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18950 | hp1 | a0001 | c0001 | t0008 | g0185 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18950 | hp2 | a0002 | c0002 | t0006 | g0323 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18951 | hp2 | a0002 | c0002 | t0044 | g0311 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18953 | hp2 | a0002 | c0002 | t0006 | g0316 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18964 | hp2 | a0002 | c0002 | t0006 | g0317 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18967 | hp1 | a0001 | c0001 | t0008 | g0177 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18967 | hp2 | a0001 | c0001 | t0009 | g0142 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18969 | hp1 | a0002 | c0002 | t0006 | g0319 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18969 | hp2 | a0001 | c0003 | t0014 | g0173 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18971 | hp1 | a0001 | c0001 | t0040 | g0048 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18971 | hp2 | a0005 | c0006 | t0001 | g0135 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18973 | hp1 | a0001 | c0001 | t0014 | g0174 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18973 | hp2 | a0002 | c0002 | t0015 | g0265 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18975 | hp1 | a0002 | c0002 | t0006 | g0329 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18978 | hp2 | a0001 | c0001 | t0061 | g0132 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18979 | hp1 | a0002 | c0002 | t0005 | g0240 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18979 | hp2 | a0001 | c0001 | t0009 | g0206 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18981 | hp1 | a0002 | c0002 | t0006 | g0313 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18982 | hp1 | a0002 | c0002 | t0006 | g0324 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18982 | hp2 | a0002 | c0002 | t0052 | g0254 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18983 | hp1 | a0001 | c0003 | t0024 | g0052 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18984 | hp1 | a0001 | c0001 | t0016 | g0031 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18984 | hp2 | a0001 | c0003 | t0076 | g0082 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18991 | hp1 | a0001 | c0003 | t0007 | g0176 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18991 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18993 | hp1 | a0001 | c0003 | t0007 | g0175 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18993 | hp2 | a0001 | c0001 | t0007 | g0218 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18994 | hp2 | a0002 | c0002 | t0006 | g0328 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0211 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19004 | hp2 | a0002 | c0002 | t0046 | g0322 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19005 | hp2 | a0001 | c0001 | t0007 | g0200 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19006 | hp1 | a0001 | c0001 | t0014 | g0201 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19006 | hp2 | a0002 | c0002 | t0015 | g0261 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19007 | hp1 | a0001 | c0001 | t0009 | g0020 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19009 | hp2 | a0001 | c0001 | t0039 | g0012 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19010 | hp1 | a0001 | c0001 | t0023 | g0062 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19010 | hp2 | a0001 | c0001 | t0023 | g0191 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19011 | hp1 | a0001 | c0003 | t0014 | g0202 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19011 | hp2 | a0001 | c0001 | t0014 | g0232 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19030 | hp1 | a0001 | c0001 | t0069 | g0047 | AFR | LWK | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19030 | hp2 | a0001 | c0001 | t0064 | g0181 | AFR | LWK | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19043 | hp1 | a0002 | c0002 | t0016 | g0024 | AFR | LWK | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19043 | hp2 | a0002 | c0002 | t0017 | g0300 | AFR | LWK | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19054 | hp2 | a0001 | c0003 | t0082 | g0134 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19056 | hp2 | a0001 | c0003 | t0043 | g0083 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19057 | hp2 | a0002 | c0002 | t0010 | g0247 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19064 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19065 | hp1 | a0002 | c0002 | t0015 | g0262 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19066 | hp1 | a0001 | c0001 | t0079 | g0058 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19066 | hp2 | a0002 | c0002 | t0006 | g0321 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19067 | hp1 | a0002 | c0002 | t0018 | g0327 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19068 | hp2 | a0002 | c0002 | t0015 | g0259 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19070 | hp1 | a0001 | c0001 | t0007 | g0138 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19070 | hp2 | a0010 | c0012 | t0009 | g0001 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19075 | hp1 | a0002 | c0002 | t0006 | g0333 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19080 | hp1 | a0001 | c0001 | t0078 | g0066 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19080 | hp2 | a0002 | c0002 | t0006 | g0312 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19081 | hp2 | a0002 | c0002 | t0045 | g0266 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19087 | hp1 | a0005 | c0006 | t0001 | g0153 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19087 | hp2 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19088 | hp1 | a0001 | c0003 | t0081 | g0006 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19089 | hp1 | a0002 | c0002 | t0047 | g0320 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19089 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19240 | hp1 | a0002 | c0002 | t0089 | g0308 | AFR | YRI | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0101 | EUR | TSI | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA20752 | hp2 | a0002 | c0002 | t0042 | g0304 | EUR | TSI | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA20905 | hp1 | a0002 | c0002 | t0005 | g0243 | SAS | GIH | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | GIH | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02109 | hp1 | a0002 | c0002 | t0019 | g0279 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02109 | hp2 | a0001 | c0001 | t0022 | g0007 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0238 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02486 | hp2 | a0002 | c0002 | t0030 | g0284 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG02559 | hp2 | a0001 | c0001 | t0021 | g0064 | AFR | ACB | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03471 | hp1 | a0002 | c0002 | t0013 | g0275 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG03471 | hp2 | a0002 | c0002 | t0028 | g0281 | AFR | MSL | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG06807 | hp1 | a0001 | c0001 | t0021 | g0039 | AFR | USA | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | USA | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA20300 | hp1 | a0002 | c0002 | t0028 | g0280 | AFR | USA | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | USA | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| NA21309 | hp2 | a0002 | c0002 | t0010 | g0287 | AFR | LWK | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0080 | REF | REF | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0005 | g0252 | REF | REF | SKIL_chr3_170352715_170401835 | SKIL | chr3 | 170352715 | 170401835 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:170360444 | C | T | 8 | a0001 a0003 a0004 others(5): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
missense_variant | MODERATE | c.113C>T | p.Ala38Val | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 795/7155 | 113/2055 | 38/684 | chr3 | 170360444 | |||
| chr3:170360534 | A | G | 1 | a0009 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.203A>G | p.His68Arg | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 885/7155 | 203/2055 | 68/684 | chr3 | 170360534 | |||
| chr3:170360536 | G | C | 1 | a0008 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.205G>C | p.Val69Leu | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 887/7155 | 205/2055 | 69/684 | chr3 | 170360536 | |||
| chr3:170360905 | A | G | 1 | a0005 | 2 | NA18971.hp2 NA19087.hp1 |
missense_variant | MODERATE | c.574A>G | p.Ile192Val | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 1256/7155 | 574/2055 | 192/684 | chr3 | 170360905 | |||
| chr3:170360929 | G | C | 1 | a0007 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.598G>C | p.Asp200His | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 1280/7155 | 598/2055 | 200/684 | chr3 | 170360929 | |||
| chr3:170381326 | C | G | 1 | a0010 | 1 | NA19070.hp2 | stop_gained | HIGH | c.1181C>G | p.Ser394* | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/7 | 1863/7155 | 1181/2055 | 394/684 | chr3 | 170381326 | |||
| chr3:170384760 | G | A | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1424G>A | p.Arg475His | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/7 | 2106/7155 | 1424/2055 | 475/684 | chr3 | 170384760 | |||
| chr3:170390318 | G | A | 1 | a0004 | 2 | HG02738.hp1 HG04115.hp1 |
missense_variant | MODERATE | c.1525G>A | p.Val509Ile | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 5/7 | 2207/7155 | 1525/2055 | 509/684 | chr3 | 170390318 | |||
| chr3:170392359 | T | A | 1 | a0003 | 2 | HG01257.hp2 HG01258.hp1 |
missense_variant | MODERATE | c.1997T>A | p.Met666Lys | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2679/7155 | 1997/2055 | 666/684 | chr3 | 170392359 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:170360628 | C | T | 1 | a0002c0009 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.297C>T | p.Ser99Ser | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 979/7155 | 297/2055 | 99/684 | chr3 | 170360628 | |||
| chr3:170360682 | G | A | 1 | a0002c0008 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.351G>A | p.Ser117Ser | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 1033/7155 | 351/2055 | 117/684 | chr3 | 170360682 | |||
| chr3:170361039 | A | G | 1 | a0001c0003 | 12 | HG00438.hp2 HG02040.hp1 NA18942.hp2 others(9): Show |
synonymous_variant | LOW | c.708A>G | p.Pro236Pro | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 1390/7155 | 708/2055 | 236/684 | chr3 | 170361039 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:170357742 | A | ACGG | 5 | a0002c0002t0017 a0002c0002t0025 a0002c0002t0026 others(2): Show |
9 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-642_-640dupCGG | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/7 | 2574 | INFO_REALIGN_3_PRIME | chr3 | 170357742 | |||||
| chr3:170359722 | A | G | 1 | a0002c0002t0089 | 1 | NA19240.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-610A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | chr3 | 170359722 | |||||||
| chr3:170359731 | G | A | 1 | a0001c0003t0043 | 1 | NA19056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-601G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 601 | chr3 | 170359731 | ||||||
| chr3:170359883 | A | G | 1 | a0002c0002t0088 | 1 | HG02055.hp2 | 5_prime_UTR_variant | MODIFIER | c.-449A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 449 | chr3 | 170359883 | ||||||
| chr3:170359925 | A | G | 63 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(60): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
5_prime_UTR_variant | MODIFIER | c.-407A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 407 | chr3 | 170359925 | ||||||
| chr3:170359987 | T | G | 6 | a0002c0002t0006 a0002c0002t0018 a0002c0002t0044 others(3): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-345T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 345 | chr3 | 170359987 | ||||||
| chr3:170360033 | T | A | 1 | a0008c0007t0048 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-299T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 299 | chr3 | 170360033 | ||||||
| chr3:170360110 | C | T | 1 | a0001c0001t0087 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-222C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 222 | chr3 | 170360110 | ||||||
| chr3:170360146 | A | G | 1 | a0001c0001t0086 | 1 | HG02698.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-186A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | chr3 | 170360146 | |||||||
| chr3:170360215 | A | G | 1 | a0001c0001t0085 | 1 | HG00609.hp2 | 5_prime_UTR_variant | MODIFIER | c.-117A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/7 | 117 | chr3 | 170360215 | ||||||
| chr3:170392481 | G | C | 1 | a0008c0007t0048 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*64G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 64 | chr3 | 170392481 | ||||||
| chr3:170392544 | T | G | 2 | a0002c0002t0049 a0002c0008t0050 |
2 | HG02976.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*127T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 127 | chr3 | 170392544 | ||||||
| chr3:170392630 | TA | T | 2 | a0001c0001t0023 a0002c0002t0047 |
4 | HG01256.hp1 NA19010.hp1 NA19010.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*220delA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 220 | INFO_REALIGN_3_PRIME | chr3 | 170392630 | |||||
| chr3:170392630 | TAA | T | 23 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0014 others(20): Show |
60 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*219_*220delAA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 219 | INFO_REALIGN_3_PRIME | chr3 | 170392630 | |||||
| chr3:170392659 | A | G | 1 | a0001c0001t0074 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*242A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 242 | chr3 | 170392659 | ||||||
| chr3:170392741 | T | A | 80 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(77): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*324T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 324 | chr3 | 170392741 | ||||||
| chr3:170392886 | T | C | 1 | a0002c0002t0057 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*469T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 469 | chr3 | 170392886 | ||||||
| chr3:170392895 | C | T | 1 | a0001c0001t0073 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*478C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 478 | chr3 | 170392895 | ||||||
| chr3:170393012 | C | T | 2 | a0001c0001t0022 a0001c0001t0074 |
4 | HG02109.hp2 HG02257.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*595C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 595 | chr3 | 170393012 | ||||||
| chr3:170393020 | C | T | 2 | a0001c0001t0040 a0001c0001t0084 |
3 | HG00423.hp2 HG00673.hp2 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*603C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 603 | chr3 | 170393020 | ||||||
| chr3:170393061 | C | G | 1 | a0002c0002t0056 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*644C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 644 | chr3 | 170393061 | ||||||
| chr3:170393115 | T | G | 2 | a0002c0002t0058 a0002c0002t0059 |
2 | HG02622.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*698T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 698 | chr3 | 170393115 | ||||||
| chr3:170393143 | A | G | 1 | a0002c0002t0055 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*726A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 726 | chr3 | 170393143 | ||||||
| chr3:170393151 | A | G | 1 | a0001c0001t0072 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*734A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 734 | chr3 | 170393151 | ||||||
| chr3:170393164 | TTTTG | T | 6 | a0002c0002t0006 a0002c0002t0018 a0002c0002t0044 others(3): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*753_*756delTTGT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 753 | INFO_REALIGN_3_PRIME | chr3 | 170393164 | |||||
| chr3:170393184 | G | A | 1 | a0001c0001t0060 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*767G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 767 | chr3 | 170393184 | ||||||
| chr3:170393278 | A | G | 6 | a0002c0002t0011 a0002c0002t0013 a0002c0002t0033 others(3): Show |
20 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*861A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 861 | chr3 | 170393278 | ||||||
| chr3:170393443 | C | T | 1 | a0001c0001t0071 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1026C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1026 | chr3 | 170393443 | ||||||
| chr3:170393522 | A | G | 2 | a0001c0001t0083 a0001c0001t0086 |
2 | HG02698.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1105A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1105 | chr3 | 170393522 | ||||||
| chr3:170393564 | A | T | 1 | a0001c0001t0070 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1147A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1147 | chr3 | 170393564 | ||||||
| chr3:170393578 | A | G | 1 | a0001c0001t0069 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1161A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1161 | chr3 | 170393578 | ||||||
| chr3:170394115 | A | AT | 4 | a0002c0002t0010 a0002c0002t0020 a0002c0002t0029 others(1): Show |
15 | HG01099.hp1 HG01361.hp2 HG02056.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1729dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1730 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | |||||
| chr3:170394115 | A | ATT | 4 | a0002c0002t0031 a0002c0002t0033 a0002c0002t0053 others(1): Show |
6 | HG01891.hp2 HG02145.hp1 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1728_*1729dupTT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1730 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | |||||
| chr3:170394115 | A | ATTT | 5 | a0002c0002t0032 a0002c0002t0034 a0002c0002t0049 others(2): Show |
6 | HG01175.hp1 HG01884.hp2 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1727_*1729dupTTT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1730 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | |||||
| chr3:170394115 | A | ATTTT | 4 | a0002c0002t0011 a0002c0002t0035 a0002c0002t0089 others(1): Show |
11 | HG02258.hp2 HG02451.hp2 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1726_*1729dupTTTT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1730 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | |||||
| chr3:170394115 | A | T | 2 | a0001c0001t0068 a0002c0002t0088 |
2 | HG02055.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1698A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1698 | chr3 | 170394115 | ||||||
| chr3:170394115 | ATT | A | 4 | a0001c0001t0021 a0001c0001t0024 a0001c0003t0024 others(1): Show |
9 | HG01358.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1728_*1729delTT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1728 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | |||||
| chr3:170394115 | ATTT | A | 11 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0060 others(8): Show |
30 | HG00423.hp2 HG00673.hp1 HG01361.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1727_*1729delTTT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1727 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | |||||
| chr3:170394115 | ATTTT | A | 31 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(28): Show |
121 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*1726_*1729delTTTT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1726 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | |||||
| chr3:170394115 | ATTTTT | A | 17 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0016 others(14): Show |
87 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1725_*1729delTTTT others(1): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1725 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | |||||
| chr3:170394115 | ATTTTTT | A | 3 | a0001c0001t0003 a0001c0001t0061 a0001c0001t0062 |
23 | HG00140.hp1 HG00280.hp1 HG01168.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1724_*1729delTTTT others(2): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1724 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | |||||
| chr3:170394115 | ATTTTTTT others(7): Show |
A | 2 | a0002c0002t0058 a0002c0002t0059 |
2 | HG02622.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1716_*1729delTTTT others(10): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1716 | INFO_REALIGN_3_PRIME | chr3 | 170394115 | |||||
| chr3:170394155 | G | A | 1 | a0002c0002t0020 | 3 | HG02257.hp1 HG02572.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1738G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1738 | chr3 | 170394155 | ||||||
| chr3:170394191 | A | G | 2 | a0001c0001t0022 a0001c0001t0074 |
4 | HG02109.hp2 HG02257.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1774A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1774 | chr3 | 170394191 | ||||||
| chr3:170394193 | C | G | 2 | a0002c0002t0058 a0002c0002t0059 |
2 | HG02622.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1776C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1776 | chr3 | 170394193 | ||||||
| chr3:170394251 | C | T | 2 | a0002c0002t0030 a0002c0002t0055 |
3 | HG02486.hp2 HG03098.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1834C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1834 | chr3 | 170394251 | ||||||
| chr3:170394355 | A | G | 1 | a0001c0001t0069 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1938A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 1938 | chr3 | 170394355 | ||||||
| chr3:170394519 | T | G | 62 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(59): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*2102T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2102 | chr3 | 170394519 | ||||||
| chr3:170394584 | G | A | 1 | a0002c0002t0041 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2167G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2167 | chr3 | 170394584 | ||||||
| chr3:170394712 | C | T | 1 | a0002c0002t0041 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2295C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2295 | chr3 | 170394712 | ||||||
| chr3:170394744 | A | G | 1 | a0002c0002t0042 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2327A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2327 | chr3 | 170394744 | ||||||
| chr3:170394894 | A | G | 1 | a0002c0002t0046 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2477A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2477 | chr3 | 170394894 | ||||||
| chr3:170395037 | T | G | 1 | a0002c0002t0052 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2620T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2620 | chr3 | 170395037 | ||||||
| chr3:170395070 | A | G | 3 | a0002c0002t0049 a0002c0002t0051 a0002c0008t0050 |
3 | HG02922.hp2 HG02976.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2653A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2653 | chr3 | 170395070 | ||||||
| chr3:170395166 | T | G | 3 | a0001c0001t0061 a0002c0002t0015 a0002c0002t0029 |
8 | HG02056.hp1 HG02080.hp2 NA18939.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2749T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2749 | chr3 | 170395166 | ||||||
| chr3:170395185 | C | T | 1 | a0001c0001t0079 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2768C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2768 | chr3 | 170395185 | ||||||
| chr3:170395268 | T | C | 1 | a0001c0001t0065 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2851T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2851 | chr3 | 170395268 | ||||||
| chr3:170395310 | G | A | 2 | a0001c0001t0022 a0001c0001t0074 |
4 | HG02109.hp2 HG02257.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2893G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2893 | chr3 | 170395310 | ||||||
| chr3:170395359 | C | T | 1 | a0001c0003t0081 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2942C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 2942 | chr3 | 170395359 | ||||||
| chr3:170395486 | A | C | 1 | a0002c0002t0041 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3069A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3069 | chr3 | 170395486 | ||||||
| chr3:170395499 | C | T | 1 | a0001c0001t0073 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3082C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3082 | chr3 | 170395499 | ||||||
| chr3:170395529 | A | G | 1 | a0001c0001t0062 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3112A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3112 | chr3 | 170395529 | ||||||
| chr3:170395689 | T | A | 1 | a0002c0002t0045 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3272T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3272 | chr3 | 170395689 | ||||||
| chr3:170395693 | G | A | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*3276G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3276 | chr3 | 170395693 | ||||||
| chr3:170395745 | G | A | 1 | a0001c0001t0063 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3328G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3328 | chr3 | 170395745 | ||||||
| chr3:170395813 | G | A | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*3396G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3396 | chr3 | 170395813 | ||||||
| chr3:170395918 | A | AT | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(50): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*3511dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3512 | INFO_REALIGN_3_PRIME | chr3 | 170395918 | |||||
| chr3:170395918 | A | ATT | 5 | a0001c0001t0012 a0001c0001t0037 a0001c0001t0039 others(2): Show |
12 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3510_*3511dupTT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3512 | INFO_REALIGN_3_PRIME | chr3 | 170395918 | |||||
| chr3:170395998 | T | C | 1 | a0001c0001t0064 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3581T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3581 | chr3 | 170395998 | ||||||
| chr3:170396010 | GT | G | 52 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(49): Show |
199 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*3609delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3609 | INFO_REALIGN_3_PRIME | chr3 | 170396010 | |||||
| chr3:170396042 | G | A | 1 | a0001c0001t0067 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3625G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3625 | chr3 | 170396042 | ||||||
| chr3:170396290 | A | C | 40 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(37): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*3873A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3873 | chr3 | 170396290 | ||||||
| chr3:170396344 | T | C | 1 | a0002c0002t0033 | 2 | HG02965.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3927T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3927 | chr3 | 170396344 | ||||||
| chr3:170396375 | A | G | 3 | a0001c0001t0078 a0001c0001t0079 a0002c0002t0019 |
5 | HG02109.hp1 HG02717.hp1 NA18522.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3958A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 3958 | chr3 | 170396375 | ||||||
| chr3:170396432 | A | G | 1 | a0002c0002t0026 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4015A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 4015 | chr3 | 170396432 | ||||||
| chr3:170396446 | T | C | 6 | a0002c0002t0015 a0002c0002t0019 a0002c0002t0020 others(3): Show |
16 | HG02056.hp1 HG02080.hp2 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4029T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 4029 | chr3 | 170396446 | ||||||
| chr3:170396622 | A | G | 1 | a0002c0002t0059 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4205A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 7/7 | 4205 | chr3 | 170396622 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:170357913 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(241): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.-634+150G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170357913 | |||||||
| chr3:170358043 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0009g0020 |
2 | NA18956.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-634+280G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358043 | |||||||
| chr3:170358045 | C | T | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(233): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-634+282C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358045 | |||||||
| chr3:170358136 | C | G | 1 | a0001c0001t0004g0239 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-634+373C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358136 | |||||||
| chr3:170358142 | C | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0016g0031 |
3 | NA18948.hp2 NA18984.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-634+379C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358142 | |||||||
| chr3:170358218 | C | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(324): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.-634+455C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358218 | |||||||
| chr3:170358227 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-634+464G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358227 | |||||||
| chr3:170358357 | C | T | 1 | a0001c0001t0008g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-634+594C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358357 | |||||||
| chr3:170358458 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0007g0015 |
2 | HG00741.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.-634+695C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358458 | |||||||
| chr3:170358495 | G | T | 3 | a0002c0002t0049g0019 a0002c0002t0051g0334 a0002c0008t0050g0019 |
3 | HG02922.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-634+732G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358495 | |||||||
| chr3:170358514 | G | A | 1 | a0001c0001t0004g0239 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-634+751G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358514 | |||||||
| chr3:170358531 | C | T | 1 | a0002c0002t0006g0333 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-634+768C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358531 | |||||||
| chr3:170358588 | C | T | 1 | a0002c0002t0033g0332 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-634+825C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358588 | |||||||
| chr3:170358783 | C | T | 24 | a0001c0001t0004g0014 a0001c0001t0004g0216 a0001c0001t0004g0219 others(21): Show |
25 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-633-916C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358783 | |||||||
| chr3:170358808 | T | C | 1 | a0002c0002t0006g0258 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-633-891T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170358808 | |||||||
| chr3:170359314 | G | A | 7 | a0002c0002t0015g0259 a0002c0002t0015g0261 a0002c0002t0015g0262 others(4): Show |
7 | HG02056.hp1 HG02080.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.-633-385G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170359314 | |||||||
| chr3:170359442 | A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-633-257A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170359442 | |||||||
| chr3:170359571 | C | T | 1 | a0001c0001t0004g0237 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-633-128C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170359571 | |||||||
| chr3:170359597 | A | G | 1 | a0001c0001t0003g0215 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-633-102A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170359597 | |||||||
| chr3:170359598 | G | A | 3 | a0001c0001t0003g0215 a0001c0001t0083g0035 a0001c0001t0086g0034 |
3 | HG01168.hp1 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-633-101G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | chr3 | 170359598 | |||||||
| chr3:170359598 | G | GA | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(215): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.-633-88dupA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 170359598 | ||||||
| chr3:170359598 | GA | G | 22 | a0002c0002t0005g0330 a0002c0002t0006g0258 a0002c0002t0006g0312 others(19): Show |
22 | HG00558.hp2 HG01255.hp2 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.-633-88delA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 170359598 | ||||||
| chr3:170361452 | T | A | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+23T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170361452 | |||||||
| chr3:170361530 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1098+101A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170361530 | |||||||
| chr3:170361594 | T | A | 9 | a0002c0002t0011g0267 a0002c0002t0011g0268 a0002c0002t0011g0269 others(6): Show |
9 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1098+165T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170361594 | |||||||
| chr3:170361742 | CT | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(235): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1098+329delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170361742 | ||||||
| chr3:170361873 | C | T | 1 | a0008c0007t0048g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1098+444C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170361873 | |||||||
| chr3:170361909 | T | G | 16 | a0002c0002t0015g0259 a0002c0002t0015g0261 a0002c0002t0015g0262 others(13): Show |
16 | HG02056.hp1 HG02080.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1098+480T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170361909 | |||||||
| chr3:170362028 | A | G | 1 | a0002c0002t0013g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1098+599A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170362028 | |||||||
| chr3:170362364 | G | A | 2 | a0001c0001t0008g0036 a0001c0001t0008g0037 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1098+935G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170362364 | |||||||
| chr3:170362462 | A | C | 2 | a0001c0001t0068g0196 a0002c0002t0088g0309 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1098+1033A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170362462 | |||||||
| chr3:170362498 | C | A | 1 | a0001c0001t0036g0038 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1098+1069C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170362498 | |||||||
| chr3:170362511 | AAAAC | A | 3 | a0001c0001t0002g0195 a0002c0002t0041g0331 a0002c0002t0089g0308 |
3 | HG02451.hp1 NA19060.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1098+1093_1098+109 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170362511 | ||||||
| chr3:170362544 | CAATG | C | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(297): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1098+1120_1098+112 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170362544 | ||||||
| chr3:170362709 | G | C | 3 | a0002c0002t0006g0312 a0002c0002t0006g0333 a0002c0002t0044g0311 |
3 | NA18951.hp2 NA19075.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1098+1280G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170362709 | |||||||
| chr3:170362778 | A | G | 12 | a0001c0001t0002g0013 a0001c0001t0002g0186 a0001c0001t0002g0187 others(9): Show |
12 | HG01433.hp1 HG01928.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.1098+1349A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170362778 | |||||||
| chr3:170362964 | C | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(259): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1098+1535C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170362964 | |||||||
| chr3:170363281 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1098+1852C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170363281 | |||||||
| chr3:170363545 | G | T | 2 | a0001c0001t0068g0196 a0002c0002t0088g0309 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1098+2116G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170363545 | |||||||
| chr3:170363546 | C | T | 24 | a0001c0001t0004g0014 a0001c0001t0004g0216 a0001c0001t0004g0219 others(21): Show |
25 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1098+2117C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170363546 | |||||||
| chr3:170363682 | G | A | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+2253G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170363682 | |||||||
| chr3:170363901 | G | T | 1 | a0001c0001t0001g0184 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1098+2472G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170363901 | |||||||
| chr3:170363983 | C | G | 1 | a0001c0001t0001g0183 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1098+2554C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170363983 | |||||||
| chr3:170364004 | G | T | 4 | a0002c0002t0005g0017 a0002c0002t0005g0256 a0002c0002t0005g0257 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+2575G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364004 | |||||||
| chr3:170364137 | G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+2708G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364137 | |||||||
| chr3:170364263 | C | G | 1 | a0002c0002t0010g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1098+2834C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364263 | |||||||
| chr3:170364311 | CT | C | 48 | a0001c0001t0068g0196 a0002c0002t0005g0003 a0002c0002t0005g0017 others(45): Show |
49 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.1098+2911delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170364311 | ||||||
| chr3:170364311 | CTTTTTT | C | 16 | a0001c0001t0001g0032 a0001c0001t0001g0179 a0001c0001t0001g0198 others(13): Show |
16 | HG00558.hp2 HG01884.hp1 HG02895.hp1 others(13): Show |
intron_variant | MODIFIER | c.1098+2906_1098+291 others(10): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170364311 | ||||||
| chr3:170364311 | CTTTTTTT | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1098+2905_1098+291 others(11): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170364311 | ||||||
| chr3:170364311 | CTTTTTTT others(1): Show |
C | 13 | a0001c0001t0001g0045 a0001c0001t0002g0043 a0001c0001t0002g0044 others(10): Show |
13 | HG01168.hp1 HG02165.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1098+2904_1098+291 others(12): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170364311 | ||||||
| chr3:170364311 | CTTTTTTT others(5): Show |
C | 19 | a0002c0002t0011g0004 a0002c0002t0011g0268 a0002c0002t0011g0269 others(16): Show |
20 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1098+2900_1098+291 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170364311 | ||||||
| chr3:170364311 | CTTTTTTT others(6): Show |
C | 1 | a0002c0002t0011g0267 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1098+2899_1098+291 others(17): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170364311 | ||||||
| chr3:170364354 | G | C | 6 | a0002c0002t0027g0298 a0002c0002t0027g0307 a0002c0002t0049g0019 others(3): Show |
6 | HG02630.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+2925G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364354 | |||||||
| chr3:170364393 | A | G | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(297): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1098+2964A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364393 | |||||||
| chr3:170364412 | C | G | 1 | a0001c0001t0008g0182 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1098+2983C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364412 | |||||||
| chr3:170364422 | C | T | 1 | a0001c0001t0004g0239 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1098+2993C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364422 | |||||||
| chr3:170364497 | G | A | 2 | a0001c0001t0068g0196 a0002c0002t0088g0309 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1098+3068G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364497 | |||||||
| chr3:170364706 | A | G | 1 | a0001c0003t0014g0173 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1098+3277A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364706 | |||||||
| chr3:170364773 | A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+3344A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364773 | |||||||
| chr3:170364877 | G | T | 1 | a0002c0002t0015g0265 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1098+3448G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364877 | |||||||
| chr3:170364887 | C | T | 337 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(334): Show |
347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1098+3458C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364887 | |||||||
| chr3:170364935 | T | A | 1 | a0001c0001t0001g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1098+3506T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170364935 | |||||||
| chr3:170365095 | C | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+3666C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365095 | |||||||
| chr3:170365165 | CAA | C | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+3737_1098+373 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365165 | |||||||
| chr3:170365512 | A | G | 7 | a0002c0002t0015g0259 a0002c0002t0015g0261 a0002c0002t0015g0262 others(4): Show |
7 | HG02056.hp1 HG02080.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.1098+4083A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365512 | |||||||
| chr3:170365752 | C | CTTT | 7 | a0002c0002t0011g0268 a0002c0002t0027g0298 a0002c0002t0027g0307 others(4): Show |
7 | HG02630.hp1 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1098+4342_1098+434 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | C | CTTTTT | 7 | a0002c0002t0017g0300 a0002c0002t0017g0303 a0002c0002t0025g0301 others(4): Show |
7 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098+4340_1098+434 others(9): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | C | CTTTTTTT others(4): Show |
1 | a0008c0007t0048g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1098+4334_1098+434 others(15): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0068g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1098+4333_1098+434 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | C | CTTTTTTT others(6): Show |
1 | a0002c0002t0088g0309 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1098+4332_1098+434 others(17): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | C | CTTTTTTT others(8): Show |
5 | a0002c0002t0011g0267 a0002c0002t0011g0269 a0002c0002t0011g0271 others(2): Show |
5 | HG01243.hp2 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+4330_1098+434 others(19): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | C | CTTTTTTT others(9): Show |
5 | a0002c0002t0011g0004 a0002c0002t0011g0273 a0002c0002t0013g0274 others(2): Show |
6 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+4329_1098+434 others(20): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | C | CTTTTTTT others(10): Show |
6 | a0002c0002t0013g0275 a0002c0002t0013g0296 a0002c0002t0013g0297 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+4328_1098+434 others(21): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | C | CTTTTTTT others(14): Show |
3 | a0002c0002t0006g0316 a0002c0002t0006g0317 a0002c0002t0045g0266 |
3 | NA18953.hp2 NA18964.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1098+4324_1098+434 others(25): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | C | CTTTTTTT others(15): Show |
6 | a0002c0002t0006g0319 a0002c0002t0006g0321 a0002c0002t0006g0323 others(3): Show |
6 | HG01978.hp1 NA18950.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+4344_1098+434 others(26): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | C | CTTTTTTT others(18): Show |
1 | a0002c0002t0006g0324 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1098+4344_1098+434 others(29): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | C | CTTTTTTT others(19): Show |
3 | a0002c0002t0006g0258 a0002c0002t0006g0325 a0002c0002t0044g0311 |
3 | HG00558.hp2 NA18949.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1098+4344_1098+434 others(30): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | C | CTTTTTTT others(20): Show |
4 | a0002c0002t0006g0326 a0002c0002t0006g0329 a0002c0002t0006g0333 others(1): Show |
4 | HG02293.hp2 NA18975.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+4344_1098+434 others(31): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | C | CTTTTTTT others(21): Show |
1 | a0002c0002t0006g0328 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1098+4344_1098+434 others(32): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | C | CTTTTTTT others(24): Show |
1 | a0002c0002t0006g0312 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1098+4344_1098+434 others(35): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | CTTT | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0172 a0001c0001t0001g0184 others(3): Show |
6 | HG00544.hp1 HG01192.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+4342_1098+434 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | CTTTT | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(88): Show |
97 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1098+4341_1098+434 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365752 | CTTTTT | C | 144 | a0001c0001t0001g0030 a0001c0001t0001g0061 a0001c0001t0001g0067 others(141): Show |
146 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1098+4340_1098+434 others(9): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170365752 | ||||||
| chr3:170365794 | C | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+4365C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365794 | |||||||
| chr3:170365796 | C | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+4367C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365796 | |||||||
| chr3:170365797 | C | T | 2 | a0001c0001t0002g0112 a0001c0001t0037g0113 |
2 | HG00140.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1098+4368C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365797 | |||||||
| chr3:170365816 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(238): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1098+4387C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365816 | |||||||
| chr3:170365841 | C | G | 51 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0015 others(48): Show |
52 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1098+4412C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365841 | |||||||
| chr3:170365941 | A | G | 5 | a0001c0003t0004g0084 a0001c0003t0007g0175 a0001c0003t0007g0176 others(2): Show |
5 | HG02040.hp1 NA18984.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+4512A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170365941 | |||||||
| chr3:170366019 | G | A | 2 | a0001c0001t0001g0115 a0006c0011t0001g0114 |
2 | HG00544.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.1098+4590G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366019 | |||||||
| chr3:170366055 | C | CT | 8 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0172 others(5): Show |
8 | HG00597.hp2 HG00609.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+4644dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366055 | ||||||
| chr3:170366055 | CT | C | 8 | a0001c0001t0001g0116 a0001c0001t0002g0085 a0001c0001t0003g0117 others(5): Show |
8 | HG00323.hp1 HG01070.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+4644delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366055 | ||||||
| chr3:170366056 | T | C | 1 | a0002c0002t0042g0304 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1098+4627T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366056 | |||||||
| chr3:170366170 | A | G | 1 | a0001c0001t0001g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1098+4741A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366170 | |||||||
| chr3:170366365 | C | T | 2 | a0002c0002t0058g0027 a0002c0002t0059g0028 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1098+4936C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366365 | |||||||
| chr3:170366388 | C | T | 3 | a0001c0001t0007g0081 a0001c0001t0083g0035 a0001c0001t0086g0034 |
3 | HG01069.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1098+4959C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366388 | |||||||
| chr3:170366415 | C | T | 2 | a0001c0001t0002g0112 a0001c0001t0037g0113 |
2 | HG00140.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1098+4986C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366415 | |||||||
| chr3:170366479 | G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+5050G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366479 | |||||||
| chr3:170366547 | A | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(275): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1098+5118A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366547 | |||||||
| chr3:170366552 | C | A | 8 | a0002c0002t0017g0299 a0002c0002t0017g0300 a0002c0002t0017g0303 others(5): Show |
8 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+5123C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366552 | |||||||
| chr3:170366688 | C | CACACACA others(7): Show |
1 | a0002c0002t0016g0022 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1098+5266_1098+526 others(18): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366688 | ||||||
| chr3:170366688 | C | CACACACA others(5): Show |
8 | a0002c0002t0016g0024 a0002c0002t0016g0025 a0002c0002t0016g0026 others(5): Show |
8 | HG01433.hp2 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1098+5266_1098+526 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366688 | ||||||
| chr3:170366688 | C | CACACACA others(3): Show |
1 | a0002c0002t0017g0303 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1098+5266_1098+526 others(14): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366688 | ||||||
| chr3:170366690 | C | CACACACA others(13): Show |
1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+5266_1098+526 others(24): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366690 | ||||||
| chr3:170366690 | C | CAG | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+5262_1098+526 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366690 | ||||||
| chr3:170366692 | C | CACACACA others(9): Show |
2 | a0001c0001t0001g0116 a0001c0001t0001g0118 |
2 | HG00323.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.1098+5266_1098+526 others(20): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366692 | ||||||
| chr3:170366692 | C | CACACAGA others(7): Show |
2 | a0001c0001t0001g0119 a0001c0001t0002g0214 |
2 | HG03669.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1098+5266_1098+526 others(18): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366692 | ||||||
| chr3:170366692 | C | CAGACACA others(3): Show |
7 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0009g0079 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1098+5264_1098+526 others(14): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366692 | ||||||
| chr3:170366694 | C | CACAGACA others(5): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0120 a0001c0001t0001g0121 |
4 | HG00639.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+5266_1098+526 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366694 | ||||||
| chr3:170366694 | C | G | 1 | a0002c0002t0005g0289 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1098+5265C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366694 | |||||||
| chr3:170366696 | G | C | 44 | a0001c0001t0001g0005 a0001c0001t0001g0116 a0001c0001t0001g0118 others(41): Show |
45 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1098+5267G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366696 | |||||||
| chr3:170366696 | G | GACAC | 5 | a0001c0001t0069g0047 a0001c0001t0072g0086 a0002c0002t0005g0288 others(2): Show |
5 | HG00423.hp1 HG02647.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+5283_1098+528 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | ||||||
| chr3:170366696 | G | GACACAC | 4 | a0002c0002t0010g0292 a0002c0002t0030g0284 a0002c0002t0030g0285 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+5281_1098+528 others(10): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | ||||||
| chr3:170366696 | G | GACACACA others(1): Show |
10 | a0002c0002t0013g0275 a0002c0002t0026g0305 a0002c0002t0026g0306 others(7): Show |
10 | HG01168.hp2 HG01169.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1098+5279_1098+528 others(12): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | ||||||
| chr3:170366696 | G | GACACACA others(3): Show |
35 | a0002c0002t0005g0290 a0002c0002t0011g0004 a0002c0002t0011g0267 others(32): Show |
36 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.1098+5277_1098+528 others(14): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | ||||||
| chr3:170366696 | G | GACACACA others(5): Show |
4 | a0001c0001t0068g0196 a0002c0002t0005g0330 a0002c0002t0019g0276 others(1): Show |
4 | HG01255.hp2 HG02055.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+5275_1098+528 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | ||||||
| chr3:170366696 | G | GACACACA others(3): Show |
10 | a0001c0001t0002g0085 a0001c0001t0002g0103 a0001c0001t0002g0105 others(7): Show |
11 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+5274_1098+527 others(14): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | ||||||
| chr3:170366696 | G | GACACACA others(5): Show |
199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(196): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1098+5274_1098+527 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | ||||||
| chr3:170366696 | G | GACACACA others(7): Show |
7 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(4): Show |
7 | HG01981.hp1 HG02970.hp2 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098+5274_1098+527 others(18): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | ||||||
| chr3:170366696 | G | GACACACA others(11): Show |
1 | a0001c0001t0004g0087 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1098+5274_1098+527 others(22): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170366696 | ||||||
| chr3:170366700 | C | G | 1 | a0002c0002t0058g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1098+5271C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366700 | |||||||
| chr3:170366716 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(239): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1098+5287T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366716 | |||||||
| chr3:170366777 | C | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+5348C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170366777 | |||||||
| chr3:170367036 | GTTTAC | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0197 |
3 | NA19056.hp1 NA19057.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1098+5610_1098+561 others(9): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170367036 | ||||||
| chr3:170367059 | C | G | 24 | a0001c0001t0004g0014 a0001c0001t0004g0216 a0001c0001t0004g0219 others(21): Show |
25 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1098+5630C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367059 | |||||||
| chr3:170367091 | T | A | 6 | a0002c0002t0027g0298 a0002c0002t0027g0307 a0002c0002t0049g0019 others(3): Show |
6 | HG02630.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+5662T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367091 | |||||||
| chr3:170367137 | C | G | 2 | a0002c0002t0015g0263 a0002c0002t0029g0264 |
2 | HG02080.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1098+5708C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367137 | |||||||
| chr3:170367149 | A | C | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(297): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1098+5720A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367149 | |||||||
| chr3:170367175 | G | C | 2 | a0001c0001t0002g0103 a0001c0001t0036g0104 |
2 | HG00639.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.1098+5746G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367175 | |||||||
| chr3:170367244 | G | T | 2 | a0001c0001t0068g0196 a0002c0002t0088g0309 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1098+5815G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367244 | |||||||
| chr3:170367343 | G | T | 2 | a0002c0002t0026g0305 a0002c0002t0026g0306 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1098+5914G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367343 | |||||||
| chr3:170367430 | C | G | 5 | a0001c0003t0004g0084 a0001c0003t0007g0175 a0001c0003t0007g0176 others(2): Show |
5 | HG02040.hp1 NA18984.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+6001C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367430 | |||||||
| chr3:170367463 | CT | C | 9 | a0002c0002t0017g0299 a0002c0002t0017g0300 a0002c0002t0017g0303 others(6): Show |
9 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1098+6049delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170367463 | ||||||
| chr3:170367464 | T | C | 1 | a0002c0002t0010g0287 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1098+6035T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367464 | |||||||
| chr3:170367476 | TTTA | T | 26 | a0001c0001t0001g0116 a0001c0001t0001g0130 a0001c0001t0001g0131 others(23): Show |
26 | HG00323.hp1 HG00558.hp2 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.1098+6048_1098+605 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367476 | |||||||
| chr3:170367477 | TTA | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(227): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1098+6049_1098+605 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367477 | |||||||
| chr3:170367478 | TA | T | 3 | a0002c0002t0041g0331 a0002c0002t0058g0027 a0002c0002t0059g0028 |
3 | HG02451.hp1 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1098+6052delA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170367478 | ||||||
| chr3:170367479 | A | T | 5 | a0002c0002t0016g0022 a0002c0002t0016g0024 a0002c0002t0016g0025 others(2): Show |
5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+6050A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367479 | |||||||
| chr3:170367481 | A | G | 3 | a0002c0002t0049g0019 a0002c0002t0051g0334 a0002c0008t0050g0019 |
3 | HG02922.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1098+6052A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367481 | |||||||
| chr3:170367623 | C | T | 1 | a0001c0001t0009g0180 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1098+6194C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367623 | |||||||
| chr3:170367624 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1098+6195A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367624 | |||||||
| chr3:170367780 | T | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1098+6351T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367780 | |||||||
| chr3:170367979 | C | T | 2 | a0002c0002t0058g0027 a0002c0002t0059g0028 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1098+6550C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170367979 | |||||||
| chr3:170368144 | A | G | 1 | a0001c0001t0007g0211 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1098+6715A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368144 | |||||||
| chr3:170368222 | G | T | 1 | a0002c0002t0006g0323 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1098+6793G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368222 | |||||||
| chr3:170368308 | A | C | 1 | a0001c0001t0001g0166 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1098+6879A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368308 | |||||||
| chr3:170368349 | A | AT | 14 | a0002c0002t0017g0299 a0002c0002t0017g0300 a0002c0002t0017g0303 others(11): Show |
14 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098+6927dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170368349 | ||||||
| chr3:170368395 | A | G | 1 | a0002c0002t0059g0028 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1098+6966A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368395 | |||||||
| chr3:170368402 | T | C | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+6973T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368402 | |||||||
| chr3:170368432 | A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+7003A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368432 | |||||||
| chr3:170368674 | GACAA | G | 7 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0169 others(4): Show |
7 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098+7250_1098+725 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170368674 | ||||||
| chr3:170368694 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1098+7265G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368694 | |||||||
| chr3:170368946 | G | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0133 |
2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1098+7517G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170368946 | |||||||
| chr3:170369082 | A | AT | 16 | a0002c0002t0005g0257 a0002c0002t0017g0300 a0002c0002t0025g0301 others(13): Show |
16 | HG01106.hp2 HG01169.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1098+7677dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170369082 | ||||||
| chr3:170369082 | A | ATT | 6 | a0002c0002t0016g0022 a0002c0002t0016g0024 a0002c0002t0016g0025 others(3): Show |
6 | HG01358.hp1 HG01433.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+7676_1098+767 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170369082 | ||||||
| chr3:170369082 | AT | A | 22 | a0002c0002t0005g0241 a0002c0002t0006g0258 a0002c0002t0006g0312 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+7677delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170369082 | ||||||
| chr3:170369082 | ATTTTTTT | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(217): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1098+7671_1098+767 others(11): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170369082 | ||||||
| chr3:170369082 | ATTTTTTT others(1): Show |
A | 9 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0012g0049 others(6): Show |
9 | HG00639.hp2 HG02280.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1098+7670_1098+767 others(12): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170369082 | ||||||
| chr3:170369274 | AAAAC | A | 4 | a0002c0002t0005g0017 a0002c0002t0005g0256 a0002c0002t0005g0257 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+7849_1098+785 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170369274 | ||||||
| chr3:170369324 | G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+7895G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170369324 | |||||||
| chr3:170369456 | C | T | 11 | a0001c0001t0008g0182 a0001c0001t0012g0049 a0001c0001t0012g0050 others(8): Show |
11 | HG00735.hp2 HG01109.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+8027C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170369456 | |||||||
| chr3:170369461 | A | AGGCAATC others(9): Show |
1 | a0002c0002t0005g0245 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1098+8033_1098+804 others(20): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170369461 | ||||||
| chr3:170369482 | A | G | 1 | a0002c0002t0005g0245 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1098+8053A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170369482 | |||||||
| chr3:170369487 | C | T | 1 | a0002c0002t0031g0250 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1098+8058C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170369487 | |||||||
| chr3:170369645 | G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+8216G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170369645 | |||||||
| chr3:170370055 | T | G | 1 | a0002c0002t0059g0028 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1098+8626T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370055 | |||||||
| chr3:170370119 | G | C | 1 | a0001c0001t0008g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1098+8690G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370119 | |||||||
| chr3:170370156 | G | A | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+8727G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370156 | |||||||
| chr3:170370224 | G | C | 24 | a0001c0001t0004g0014 a0001c0001t0004g0216 a0001c0001t0004g0219 others(21): Show |
25 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1098+8795G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370224 | |||||||
| chr3:170370233 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1098+8804C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370233 | |||||||
| chr3:170370320 | A | G | 1 | a0002c0002t0089g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1098+8891A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370320 | |||||||
| chr3:170370404 | A | G | 1 | a0002c0002t0005g0249 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1098+8975A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370404 | |||||||
| chr3:170370421 | C | CAG | 53 | a0001c0001t0001g0061 a0001c0001t0002g0013 a0001c0001t0002g0015 others(50): Show |
54 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.1098+9009_1098+901 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170370421 | ||||||
| chr3:170370432 | A | C | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+9003A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370432 | |||||||
| chr3:170370438 | A | C | 8 | a0002c0002t0005g0245 a0002c0002t0017g0299 a0002c0002t0017g0300 others(5): Show |
8 | HG01358.hp1 HG02071.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+9009A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370438 | |||||||
| chr3:170370439 | G | C | 2 | a0002c0002t0005g0245 a0002c0002t0010g0246 |
2 | HG02071.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1098+9010G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370439 | |||||||
| chr3:170370439 | G | GA | 23 | a0001c0001t0002g0008 a0001c0001t0002g0044 a0001c0001t0002g0112 others(20): Show |
25 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.1098+9010_1098+901 others(5): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370439 | |||||||
| chr3:170370439 | G | GAGC | 38 | a0001c0001t0002g0085 a0001c0001t0002g0091 a0001c0001t0002g0092 others(35): Show |
38 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1098+9010_1098+901 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370439 | |||||||
| chr3:170370439 | G | GAGCC | 8 | a0001c0001t0002g0103 a0001c0001t0002g0195 a0001c0001t0004g0216 others(5): Show |
8 | HG00642.hp2 HG00741.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+9010_1098+901 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370439 | |||||||
| chr3:170370439 | G | GC | 16 | a0001c0001t0001g0033 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
16 | HG00639.hp2 HG01175.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1098+9026dupC | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170370439 | ||||||
| chr3:170370439 | GC | G | 35 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
36 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1098+9026delC | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170370439 | ||||||
| chr3:170370439 | GCC | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(52): Show |
59 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.1098+9025_1098+902 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170370439 | ||||||
| chr3:170370439 | GCCC | G | 17 | a0001c0001t0063g0165 a0001c0001t0068g0196 a0002c0002t0005g0290 others(14): Show |
17 | HG00735.hp1 HG01433.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1098+9024_1098+902 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170370439 | ||||||
| chr3:170370439 | GCCCC | G | 26 | a0002c0002t0011g0004 a0002c0002t0011g0267 a0002c0002t0011g0268 others(23): Show |
27 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1098+9023_1098+902 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170370439 | ||||||
| chr3:170370440 | C | A | 29 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0169 others(26): Show |
29 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.1098+9011C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370440 | |||||||
| chr3:170370440 | C | G | 23 | a0001c0001t0002g0008 a0001c0001t0002g0044 a0001c0001t0002g0112 others(20): Show |
25 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.1098+9011C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370440 | |||||||
| chr3:170370441 | C | A | 3 | a0002c0002t0015g0263 a0002c0002t0015g0265 a0002c0002t0029g0264 |
3 | HG02080.hp2 NA18939.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1098+9012C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370441 | |||||||
| chr3:170370441 | C | G | 31 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0169 others(28): Show |
31 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.1098+9012C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370441 | |||||||
| chr3:170370442 | C | G | 3 | a0002c0002t0015g0263 a0002c0002t0015g0265 a0002c0002t0029g0264 |
3 | HG02080.hp2 NA18939.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1098+9013C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370442 | |||||||
| chr3:170370442 | C | T | 1 | a0002c0002t0005g0330 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1098+9013C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370442 | |||||||
| chr3:170370443 | C | G | 1 | a0002c0002t0013g0297 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1098+9014C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370443 | |||||||
| chr3:170370443 | C | T | 1 | a0002c0002t0005g0290 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1098+9014C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370443 | |||||||
| chr3:170370449 | C | A | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+9020C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370449 | |||||||
| chr3:170370450 | C | A | 1 | a0002c0002t0020g0277 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1098+9021C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370450 | |||||||
| chr3:170370451 | C | A | 6 | a0001c0001t0004g0014 a0001c0001t0004g0219 a0001c0001t0004g0220 others(3): Show |
7 | NA18747.hp1 NA18942.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1098+9022C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370451 | |||||||
| chr3:170370453 | C | T | 2 | a0002c0002t0015g0261 a0002c0002t0015g0262 |
2 | NA19006.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1098+9024C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370453 | |||||||
| chr3:170370456 | G | C | 1 | a0001c0001t0077g0221 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1098+9027G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370456 | |||||||
| chr3:170370492 | A | G | 1 | a0001c0001t0021g0039 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1098+9063A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370492 | |||||||
| chr3:170370660 | C | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1098+9231C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370660 | |||||||
| chr3:170370819 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1098+9390C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370819 | |||||||
| chr3:170370855 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1098+9426G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170370855 | |||||||
| chr3:170371008 | A | G | 6 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0328 others(3): Show |
6 | HG00558.hp2 NA18951.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+9579A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371008 | |||||||
| chr3:170371025 | T | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+9596T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371025 | |||||||
| chr3:170371191 | G | A | 1 | a0002c0002t0052g0254 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1098+9762G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371191 | |||||||
| chr3:170371327 | C | T | 1 | a0001c0001t0007g0063 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1098+9898C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371327 | |||||||
| chr3:170371351 | A | T | 1 | a0002c0002t0019g0212 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1099-9893A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371351 | |||||||
| chr3:170371379 | C | T | 6 | a0001c0001t0003g0117 a0001c0001t0003g0127 a0001c0001t0003g0149 others(3): Show |
6 | HG01261.hp1 HG01981.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-9865C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371379 | |||||||
| chr3:170371536 | A | G | 1 | a0008c0007t0048g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1099-9708A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371536 | |||||||
| chr3:170371567 | T | G | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-9677T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170371567 | |||||||
| chr3:170372105 | ATTAAG | A | 9 | a0002c0002t0006g0313 a0002c0002t0006g0315 a0002c0002t0006g0317 others(6): Show |
9 | HG02071.hp2 HG03831.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-9136_1099-913 others(9): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170372105 | ||||||
| chr3:170372218 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1099-9026A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372218 | |||||||
| chr3:170372586 | A | G | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(297): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1099-8658A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372586 | |||||||
| chr3:170372599 | C | G | 1 | a0002c0002t0005g0330 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1099-8645C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372599 | |||||||
| chr3:170372615 | G | A | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-8629G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372615 | |||||||
| chr3:170372767 | T | C | 1 | a0002c0002t0089g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1099-8477T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372767 | |||||||
| chr3:170372895 | A | G | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-8349A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372895 | |||||||
| chr3:170372944 | C | T | 5 | a0002c0002t0016g0022 a0002c0002t0016g0024 a0002c0002t0016g0025 others(2): Show |
5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-8300C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372944 | |||||||
| chr3:170372973 | T | C | 6 | a0002c0002t0027g0298 a0002c0002t0027g0307 a0002c0002t0049g0019 others(3): Show |
6 | HG02630.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-8271T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372973 | |||||||
| chr3:170372988 | A | AT | 78 | a0001c0001t0001g0137 a0001c0001t0002g0008 a0001c0001t0002g0013 others(75): Show |
79 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1099-8239dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170372988 | ||||||
| chr3:170372988 | A | ATT | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(183): Show |
193 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1099-8240_1099-823 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170372988 | ||||||
| chr3:170372988 | A | T | 2 | a0002c0002t0026g0305 a0002c0002t0026g0306 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1099-8256A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170372988 | |||||||
| chr3:170373049 | G | A | 8 | a0001c0001t0001g0067 a0001c0001t0003g0117 a0001c0001t0003g0127 others(5): Show |
8 | HG01070.hp1 HG01261.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-8195G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373049 | |||||||
| chr3:170373066 | C | T | 1 | a0001c0001t0069g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1099-8178C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373066 | |||||||
| chr3:170373205 | C | T | 2 | a0002c0002t0058g0027 a0002c0002t0059g0028 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1099-8039C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373205 | |||||||
| chr3:170373214 | T | C | 1 | a0001c0001t0003g0170 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1099-8030T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373214 | |||||||
| chr3:170373260 | G | A | 1 | a0005c0006t0001g0153 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1099-7984G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373260 | |||||||
| chr3:170373325 | C | T | 2 | a0002c0002t0058g0027 a0002c0002t0059g0028 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1099-7919C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373325 | |||||||
| chr3:170373387 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1099-7857C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373387 | |||||||
| chr3:170373422 | T | TC | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1099-7820dupC | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170373422 | ||||||
| chr3:170373545 | T | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(238): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1099-7699T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373545 | |||||||
| chr3:170373701 | A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-7543A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373701 | |||||||
| chr3:170373722 | CAAAAAAA others(4): Show |
C | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-7510_1099-750 others(15): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170373722 | ||||||
| chr3:170373741 | A | G | 1 | a0001c0001t0002g0193 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1099-7503A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373741 | |||||||
| chr3:170373796 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(238): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1099-7448C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373796 | |||||||
| chr3:170373856 | T | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1099-7388T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373856 | |||||||
| chr3:170373884 | A | G | 1 | a0001c0001t0069g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1099-7360A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373884 | |||||||
| chr3:170373958 | C | G | 8 | a0002c0002t0017g0299 a0002c0002t0017g0300 a0002c0002t0017g0303 others(5): Show |
8 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-7286C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170373958 | |||||||
| chr3:170374047 | A | T | 1 | a0001c0001t0036g0038 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1099-7197A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170374047 | |||||||
| chr3:170374060 | G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-7184G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170374060 | |||||||
| chr3:170374114 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(277): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1099-7130C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170374114 | |||||||
| chr3:170374265 | AG | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(275): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1099-6977delG | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170374265 | ||||||
| chr3:170374269 | A | C | 51 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0015 others(48): Show |
52 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1099-6975A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170374269 | |||||||
| chr3:170374293 | G | A | 2 | a0003c0005t0012g0071 a0003c0005t0012g0075 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1099-6951G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170374293 | |||||||
| chr3:170374451 | A | G | 1 | a0001c0001t0014g0232 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1099-6793A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170374451 | |||||||
| chr3:170374919 | A | C | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-6325A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170374919 | |||||||
| chr3:170375020 | A | T | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-6224A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375020 | |||||||
| chr3:170375175 | T | G | 2 | a0002c0002t0016g0022 a0002c0002t0057g0023 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1099-6069T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375175 | |||||||
| chr3:170375271 | A | C | 2 | a0002c0002t0058g0027 a0002c0002t0059g0028 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1099-5973A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375271 | |||||||
| chr3:170375296 | A | G | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-5948A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375296 | |||||||
| chr3:170375340 | T | C | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-5904T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375340 | |||||||
| chr3:170375363 | G | T | 4 | a0001c0001t0022g0007 a0001c0001t0022g0042 a0001c0001t0022g0078 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-5881G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375363 | |||||||
| chr3:170375364 | C | A | 4 | a0001c0001t0022g0007 a0001c0001t0022g0042 a0001c0001t0022g0078 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-5880C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375364 | |||||||
| chr3:170375364 | C | G | 1 | a0001c0001t0023g0062 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1099-5880C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375364 | |||||||
| chr3:170375365 | T | A | 1 | a0001c0001t0023g0062 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1099-5879T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375365 | |||||||
| chr3:170375459 | G | C | 1 | a0001c0001t0009g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1099-5785G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375459 | |||||||
| chr3:170375542 | A | C | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-5702A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375542 | |||||||
| chr3:170375569 | A | G | 6 | a0002c0002t0027g0298 a0002c0002t0027g0307 a0002c0002t0049g0019 others(3): Show |
6 | HG02630.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-5675A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375569 | |||||||
| chr3:170375592 | C | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-5652C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375592 | |||||||
| chr3:170375731 | C | T | 2 | a0002c0002t0027g0298 a0002c0002t0027g0307 |
2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1099-5513C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375731 | |||||||
| chr3:170375751 | A | AT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(94): Show |
102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1099-5485dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170375751 | ||||||
| chr3:170375800 | G | A | 1 | a0001c0001t0040g0055 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1099-5444G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375800 | |||||||
| chr3:170375917 | T | G | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-5327T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375917 | |||||||
| chr3:170375972 | A | C | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-5272A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170375972 | |||||||
| chr3:170376042 | C | CT | 16 | a0001c0001t0002g0091 a0001c0001t0002g0192 a0001c0001t0004g0220 others(13): Show |
16 | HG00423.hp2 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099-5179dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170376042 | ||||||
| chr3:170376042 | CT | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(121): Show |
128 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1099-5179delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170376042 | ||||||
| chr3:170376042 | CTT | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0032 others(22): Show |
27 | HG00639.hp2 HG01884.hp2 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1099-5180_1099-517 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170376042 | ||||||
| chr3:170376042 | CTTTTTTT others(7): Show |
C | 1 | a0002c0009t0032g0286 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1099-5192_1099-517 others(18): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170376042 | ||||||
| chr3:170376101 | G | A | 2 | a0002c0002t0027g0298 a0002c0002t0027g0307 |
2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1099-5143G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376101 | |||||||
| chr3:170376197 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1099-5047A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376197 | |||||||
| chr3:170376274 | G | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1099-4970G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376274 | |||||||
| chr3:170376340 | C | A | 1 | a0008c0007t0048g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1099-4904C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376340 | |||||||
| chr3:170376371 | A | G | 1 | a0001c0001t0004g0230 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1099-4873A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376371 | |||||||
| chr3:170376402 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1099-4842G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376402 | |||||||
| chr3:170376471 | T | G | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-4773T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376471 | |||||||
| chr3:170376472 | G | T | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-4772G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376472 | |||||||
| chr3:170376473 | T | G | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-4771T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376473 | |||||||
| chr3:170376529 | C | A | 1 | a0002c0002t0089g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1099-4715C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376529 | |||||||
| chr3:170376603 | T | C | 1 | a0002c0002t0005g0243 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1099-4641T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376603 | |||||||
| chr3:170376692 | T | G | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-4552T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376692 | |||||||
| chr3:170376787 | G | T | 3 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0169 |
3 | HG00597.hp2 HG00609.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.1099-4457G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376787 | |||||||
| chr3:170376795 | CA | C | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-4446delA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170376795 | ||||||
| chr3:170376872 | G | T | 2 | a0001c0001t0068g0196 a0002c0002t0088g0309 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1099-4372G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376872 | |||||||
| chr3:170376875 | T | C | 2 | a0001c0001t0004g0225 a0001c0001t0004g0226 |
2 | HG01192.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1099-4369T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376875 | |||||||
| chr3:170376936 | A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-4308A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170376936 | |||||||
| chr3:170377025 | C | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-4219C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377025 | |||||||
| chr3:170377120 | T | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1099-4124T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377120 | |||||||
| chr3:170377125 | C | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-4119C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377125 | |||||||
| chr3:170377147 | A | G | 2 | a0001c0001t0004g0229 a0001c0001t0075g0234 |
2 | HG00323.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1099-4097A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377147 | |||||||
| chr3:170377231 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1099-4013G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377231 | |||||||
| chr3:170377245 | T | C | 1 | a0001c0001t0003g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1099-3999T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377245 | |||||||
| chr3:170377357 | T | C | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(297): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1099-3887T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377357 | |||||||
| chr3:170377398 | C | CT | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1099-3831dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170377398 | ||||||
| chr3:170377493 | T | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(277): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1099-3751T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377493 | |||||||
| chr3:170377542 | C | CT | 31 | a0001c0001t0001g0033 a0001c0001t0001g0148 a0001c0001t0001g0197 others(28): Show |
31 | HG00597.hp2 HG01168.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.1099-3678dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170377542 | ||||||
| chr3:170377542 | CT | C | 15 | a0001c0001t0001g0030 a0001c0001t0001g0144 a0001c0001t0004g0225 others(12): Show |
15 | HG01169.hp1 HG01433.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.1099-3678delT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170377542 | ||||||
| chr3:170377542 | CTTTTTTT others(6): Show |
C | 3 | a0002c0002t0019g0212 a0002c0002t0019g0276 a0002c0002t0019g0279 |
3 | HG02109.hp1 HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1099-3690_1099-367 others(17): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170377542 | ||||||
| chr3:170377631 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1099-3613C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377631 | |||||||
| chr3:170377639 | T | A | 1 | a0002c0002t0006g0328 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1099-3605T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377639 | |||||||
| chr3:170377652 | G | A | 1 | a0002c0002t0017g0303 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1099-3592G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377652 | |||||||
| chr3:170377696 | C | CT | 3 | a0001c0001t0002g0043 a0001c0001t0002g0100 a0001c0001t0002g0195 |
3 | NA18994.hp1 NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1099-3547dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170377696 | ||||||
| chr3:170377936 | C | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-3308C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170377936 | |||||||
| chr3:170378110 | C | T | 3 | a0002c0002t0020g0277 a0002c0002t0020g0278 a0002c0002t0020g0283 |
3 | HG02257.hp1 HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1099-3134C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378110 | |||||||
| chr3:170378126 | C | T | 130 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0015 others(127): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1099-3118C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378126 | |||||||
| chr3:170378169 | G | A | 1 | a0002c0002t0005g0255 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1099-3075G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378169 | |||||||
| chr3:170378184 | CCCTG | C | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-3056_1099-305 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378184 | ||||||
| chr3:170378303 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1099-2941G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378303 | |||||||
| chr3:170378315 | G | C | 4 | a0002c0002t0017g0299 a0002c0002t0017g0300 a0002c0002t0025g0301 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-2929G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378315 | |||||||
| chr3:170378364 | T | G | 1 | a0001c0001t0002g0093 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1099-2880T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378364 | |||||||
| chr3:170378509 | C | T | 5 | a0002c0002t0016g0022 a0002c0002t0016g0024 a0002c0002t0016g0025 others(2): Show |
5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-2735C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378509 | |||||||
| chr3:170378549 | C | CTT | 24 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0315 others(21): Show |
24 | HG00558.hp2 HG01433.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1099-2694_1099-269 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378549 | ||||||
| chr3:170378551 | C | T | 26 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0315 others(23): Show |
26 | HG00558.hp2 HG01433.hp2 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.1099-2693C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378551 | |||||||
| chr3:170378553 | C | CTTTTTT | 15 | a0001c0001t0001g0116 a0001c0001t0001g0154 a0001c0001t0001g0172 others(12): Show |
15 | HG00323.hp1 HG01069.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1099-2681_1099-267 others(10): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378553 | ||||||
| chr3:170378553 | C | CTTTTTTT | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(199): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1099-2682_1099-267 others(11): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378553 | ||||||
| chr3:170378553 | C | CTTTTTTT others(1): Show |
13 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0148 others(10): Show |
13 | HG01175.hp2 HG01192.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.1099-2683_1099-267 others(12): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378553 | ||||||
| chr3:170378553 | C | T | 27 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(24): Show |
27 | HG00558.hp2 HG01433.hp2 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.1099-2691C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378553 | |||||||
| chr3:170378583 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1099-2661G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378583 | |||||||
| chr3:170378668 | C | T | 1 | a0002c0002t0019g0279 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1099-2576C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378668 | |||||||
| chr3:170378692 | C | T | 1 | a0001c0001t0004g0231 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1099-2552C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378692 | |||||||
| chr3:170378705 | C | G | 8 | a0002c0002t0017g0299 a0002c0002t0017g0300 a0002c0002t0017g0303 others(5): Show |
8 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-2539C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378705 | |||||||
| chr3:170378708 | T | C | 11 | a0001c0001t0008g0182 a0001c0001t0012g0049 a0001c0001t0012g0050 others(8): Show |
11 | HG00735.hp2 HG01109.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1099-2536T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378708 | |||||||
| chr3:170378835 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1099-2409A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378835 | |||||||
| chr3:170378849 | TTTTA | T | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(322): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1099-2363_1099-236 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378849 | ||||||
| chr3:170378849 | TTTTATTT others(1): Show |
T | 3 | a0001c0001t0001g0120 a0001c0001t0068g0196 a0002c0002t0088g0309 |
3 | HG00639.hp2 HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1099-2367_1099-236 others(12): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378849 | ||||||
| chr3:170378881 | A | T | 9 | a0001c0001t0071g0040 a0002c0002t0016g0022 a0002c0002t0016g0024 others(6): Show |
9 | HG01433.hp2 HG02486.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1099-2363A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378881 | |||||||
| chr3:170378881 | ATTTT | A | 12 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0004g0014 others(9): Show |
13 | HG01884.hp1 HG02257.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1099-2358_1099-235 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170378881 | ||||||
| chr3:170378885 | T | A | 1 | a0002c0002t0058g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1099-2359T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170378885 | |||||||
| chr3:170379002 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1099-2242G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379002 | |||||||
| chr3:170379073 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1099-2171C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379073 | |||||||
| chr3:170379077 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(277): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1099-2167G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379077 | |||||||
| chr3:170379136 | C | T | 8 | a0001c0001t0012g0049 a0001c0001t0012g0050 a0001c0001t0012g0070 others(5): Show |
8 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-2108C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379136 | |||||||
| chr3:170379230 | G | A | 7 | a0001c0001t0001g0033 a0002c0002t0027g0298 a0002c0002t0027g0307 others(4): Show |
7 | HG02145.hp2 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1099-2014G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379230 | |||||||
| chr3:170379265 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1099-1979A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379265 | |||||||
| chr3:170379267 | T | C | 1 | a0001c0001t0021g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1099-1977T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379267 | |||||||
| chr3:170379484 | C | CCT | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(260): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1099-1759_1099-175 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170379484 | ||||||
| chr3:170379667 | C | T | 2 | a0002c0002t0028g0281 a0002c0002t0053g0282 |
2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1099-1577C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379667 | |||||||
| chr3:170379685 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1099-1559C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379685 | |||||||
| chr3:170379690 | C | T | 1 | a0002c0002t0006g0323 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1099-1554C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379690 | |||||||
| chr3:170379724 | C | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(276): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1099-1520C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379724 | |||||||
| chr3:170379818 | G | A | 74 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0015 others(71): Show |
75 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1099-1426G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379818 | |||||||
| chr3:170379855 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0002g0093 a0001c0001t0008g0177 |
4 | NA18951.hp1 NA18953.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-1389G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379855 | |||||||
| chr3:170379893 | C | T | 1 | a0001c0001t0004g0225 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1099-1351C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379893 | |||||||
| chr3:170379906 | A | G | 1 | a0002c0002t0010g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1099-1338A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379906 | |||||||
| chr3:170379938 | C | T | 4 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0169 others(1): Show |
4 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-1306C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379938 | |||||||
| chr3:170379946 | T | C | 1 | a0002c0002t0058g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1099-1298T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170379946 | |||||||
| chr3:170380050 | A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-1194A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380050 | |||||||
| chr3:170380054 | C | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1099-1190C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380054 | |||||||
| chr3:170380067 | T | C | 2 | a0002c0002t0058g0027 a0002c0002t0059g0028 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1099-1177T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380067 | |||||||
| chr3:170380212 | G | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-1032G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380212 | |||||||
| chr3:170380395 | C | T | 1 | a0001c0001t0003g0178 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1099-849C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380395 | |||||||
| chr3:170380494 | A | G | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-750A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380494 | |||||||
| chr3:170380567 | C | T | 1 | a0001c0001t0069g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1099-677C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380567 | |||||||
| chr3:170380600 | G | A | 7 | a0002c0002t0015g0259 a0002c0002t0015g0261 a0002c0002t0015g0262 others(4): Show |
7 | HG02056.hp1 HG02080.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.1099-644G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380600 | |||||||
| chr3:170380603 | A | C | 1 | a0001c0003t0014g0202 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1099-641A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380603 | |||||||
| chr3:170380651 | A | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(95): Show |
103 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1099-593A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380651 | |||||||
| chr3:170380655 | A | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(265): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1099-589A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380655 | |||||||
| chr3:170380659 | T | A | 2 | a0001c0001t0068g0196 a0002c0002t0088g0309 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1099-585T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380659 | |||||||
| chr3:170380704 | A | T | 1 | a0001c0001t0002g0099 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1099-540A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380704 | |||||||
| chr3:170380892 | A | G | 1 | a0001c0001t0063g0165 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1099-352A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170380892 | |||||||
| chr3:170380995 | A | AT | 41 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0116 others(38): Show |
41 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-230dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170380995 | ||||||
| chr3:170380995 | A | ATT | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(195): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1099-231_1099-230d others(4): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170380995 | ||||||
| chr3:170380995 | A | ATTT | 30 | a0001c0001t0001g0167 a0001c0001t0001g0210 a0001c0001t0002g0013 others(27): Show |
30 | HG00558.hp1 HG00673.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1099-232_1099-230d others(5): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 170380995 | ||||||
| chr3:170381047 | T | C | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-197T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170381047 | |||||||
| chr3:170381201 | A | G | 1 | a0002c0002t0056g0244 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1099-43A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 2/6 | chr3 | 170381201 | |||||||
| chr3:170381380 | C | T | 2 | a0002c0002t0058g0027 a0002c0002t0059g0028 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1196+39C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381380 | |||||||
| chr3:170381430 | A | G | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1196+89A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381430 | |||||||
| chr3:170381430 | ATTAT | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(93): Show |
101 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1196+100_1196+103d others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170381430 | ||||||
| chr3:170381564 | C | T | 1 | a0001c0001t0084g0060 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1196+223C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381564 | |||||||
| chr3:170381590 | G | A | 6 | a0002c0002t0005g0240 a0002c0002t0005g0249 a0002c0002t0005g0255 others(3): Show |
6 | HG01081.hp2 HG01928.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1196+249G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381590 | |||||||
| chr3:170381605 | T | G | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(297): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1196+264T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381605 | |||||||
| chr3:170381628 | T | A | 1 | a0001c0001t0064g0181 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1196+287T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381628 | |||||||
| chr3:170381725 | G | T | 1 | a0004c0004t0004g0223 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1196+384G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381725 | |||||||
| chr3:170381819 | T | C | 1 | a0001c0003t0076g0082 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1196+478T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381819 | |||||||
| chr3:170381877 | C | T | 1 | a0002c0002t0089g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1196+536C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381877 | |||||||
| chr3:170381945 | G | C | 2 | a0001c0001t0068g0196 a0002c0002t0088g0309 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1196+604G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381945 | |||||||
| chr3:170381965 | C | T | 19 | a0002c0002t0011g0004 a0002c0002t0011g0267 a0002c0002t0011g0268 others(16): Show |
20 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1196+624C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381965 | |||||||
| chr3:170381971 | A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1196+630A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170381971 | |||||||
| chr3:170382036 | C | T | 17 | a0002c0002t0011g0004 a0002c0002t0011g0267 a0002c0002t0011g0268 others(14): Show |
18 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1196+695C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382036 | |||||||
| chr3:170382168 | G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1196+827G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382168 | |||||||
| chr3:170382261 | TTTGAAA | T | 5 | a0002c0002t0016g0022 a0002c0002t0016g0024 a0002c0002t0016g0025 others(2): Show |
5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+922_1196+927d others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170382261 | ||||||
| chr3:170382269 | A | C | 5 | a0002c0002t0016g0022 a0002c0002t0016g0024 a0002c0002t0016g0025 others(2): Show |
5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+928A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382269 | |||||||
| chr3:170382413 | A | AT | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
110 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1196+1091dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170382413 | ||||||
| chr3:170382413 | A | ATT | 7 | a0001c0001t0001g0032 a0001c0001t0001g0119 a0001c0001t0001g0131 others(4): Show |
7 | HG02622.hp1 HG02723.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1196+1090_1196+109 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170382413 | ||||||
| chr3:170382416 | T | TA | 128 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0015 others(125): Show |
131 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1196+1075_1196+107 others(5): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382416 | |||||||
| chr3:170382417 | T | A | 1 | a0001c0001t0007g0081 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1196+1076T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382417 | |||||||
| chr3:170382556 | G | T | 5 | a0002c0002t0016g0022 a0002c0002t0016g0024 a0002c0002t0016g0025 others(2): Show |
5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+1215G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382556 | |||||||
| chr3:170382557 | C | A | 20 | a0002c0002t0011g0004 a0002c0002t0011g0267 a0002c0002t0011g0268 others(17): Show |
21 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1196+1216C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382557 | |||||||
| chr3:170382659 | G | A | 7 | a0002c0002t0016g0022 a0002c0002t0016g0024 a0002c0002t0016g0025 others(4): Show |
7 | HG01433.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1196+1318G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382659 | |||||||
| chr3:170382688 | T | C | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(317): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.1196+1347T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382688 | |||||||
| chr3:170382718 | A | AT | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1196+1395dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170382718 | ||||||
| chr3:170382718 | A | ATT | 16 | a0001c0001t0001g0124 a0001c0001t0001g0131 a0001c0001t0001g0168 others(13): Show |
16 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.1196+1394_1196+139 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170382718 | ||||||
| chr3:170382749 | C | T | 1 | a0002c0002t0053g0282 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1196+1408C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382749 | |||||||
| chr3:170382875 | C | T | 5 | a0002c0002t0006g0316 a0002c0002t0006g0319 a0002c0002t0045g0266 others(2): Show |
5 | NA18953.hp2 NA18969.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+1534C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170382875 | |||||||
| chr3:170383028 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1197-1505T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383028 | |||||||
| chr3:170383058 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1197-1475T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383058 | |||||||
| chr3:170383078 | G | A | 1 | a0001c0001t0002g0097 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1197-1455G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383078 | |||||||
| chr3:170383116 | G | C | 1 | a0001c0001t0001g0207 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1197-1417G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383116 | |||||||
| chr3:170383252 | G | A | 1 | a0001c0001t0003g0157 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1197-1281G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383252 | |||||||
| chr3:170383330 | A | C | 7 | a0002c0002t0016g0022 a0002c0002t0016g0024 a0002c0002t0016g0025 others(4): Show |
7 | HG01433.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1197-1203A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383330 | |||||||
| chr3:170383475 | T | C | 16 | a0002c0002t0015g0259 a0002c0002t0015g0261 a0002c0002t0015g0262 others(13): Show |
16 | HG02056.hp1 HG02080.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1197-1058T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383475 | |||||||
| chr3:170383646 | G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1197-887G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383646 | |||||||
| chr3:170383649 | G | A | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1197-884G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383649 | |||||||
| chr3:170383912 | G | T | 1 | a0001c0001t0009g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1197-621G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | chr3 | 170383912 | |||||||
| chr3:170384037 | C | CA | 29 | a0001c0001t0001g0033 a0001c0001t0001g0137 a0001c0001t0004g0225 others(26): Show |
30 | HG01192.hp2 HG01255.hp1 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.1197-481dupA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170384037 | ||||||
| chr3:170384037 | CA | C | 32 | a0001c0001t0001g0129 a0001c0001t0001g0198 a0001c0001t0001g0199 others(29): Show |
32 | HG00558.hp2 HG01433.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1197-481delA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 170384037 | ||||||
| chr3:170384920 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0067g0139 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1429+155T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170384920 | |||||||
| chr3:170384961 | A | G | 6 | a0001c0001t0003g0117 a0001c0001t0003g0127 a0001c0001t0003g0149 others(3): Show |
6 | HG01261.hp1 HG01981.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1429+196A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170384961 | |||||||
| chr3:170384991 | C | T | 2 | a0002c0002t0010g0287 a0002c0009t0032g0286 |
2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1429+226C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170384991 | |||||||
| chr3:170385134 | C | T | 8 | a0001c0001t0012g0049 a0001c0001t0012g0050 a0001c0001t0012g0070 others(5): Show |
8 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429+369C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170385134 | |||||||
| chr3:170385171 | G | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1429+406G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170385171 | |||||||
| chr3:170385257 | A | AT | 23 | a0001c0001t0001g0033 a0001c0001t0001g0131 a0001c0001t0001g0148 others(20): Show |
23 | HG01106.hp2 HG01175.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1429+509dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170385257 | ||||||
| chr3:170385258 | T | A | 1 | a0001c0001t0014g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1429+493T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170385258 | |||||||
| chr3:170385536 | A | G | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1429+771A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170385536 | |||||||
| chr3:170385595 | G | A | 4 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0004g0228 others(1): Show |
4 | HG01192.hp2 HG01993.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429+830G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170385595 | |||||||
| chr3:170385804 | T | C | 130 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0015 others(127): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1429+1039T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170385804 | |||||||
| chr3:170385954 | C | G | 1 | a0002c0002t0059g0028 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1429+1189C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170385954 | |||||||
| chr3:170386035 | G | A | 1 | a0002c0002t0013g0270 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1429+1270G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386035 | |||||||
| chr3:170386123 | T | G | 1 | a0002c0002t0020g0283 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1429+1358T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386123 | |||||||
| chr3:170386123 | T | TTTTG | 4 | a0001c0001t0004g0087 a0001c0001t0008g0090 a0001c0001t0065g0094 others(1): Show |
4 | HG01361.hp1 HG01934.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429+1379_1429+138 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170386123 | ||||||
| chr3:170386143 | G | T | 2 | a0002c0002t0058g0027 a0002c0002t0059g0028 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1429+1378G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386143 | |||||||
| chr3:170386225 | G | C | 130 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0015 others(127): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1429+1460G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386225 | |||||||
| chr3:170386287 | C | T | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1429+1522C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386287 | |||||||
| chr3:170386318 | C | T | 1 | a0002c0002t0006g0326 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1429+1553C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386318 | |||||||
| chr3:170386319 | G | A | 5 | a0002c0002t0016g0022 a0002c0002t0016g0024 a0002c0002t0016g0025 others(2): Show |
5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1429+1554G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386319 | |||||||
| chr3:170386382 | G | A | 2 | a0002c0002t0058g0027 a0002c0002t0059g0028 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1429+1617G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386382 | |||||||
| chr3:170386390 | A | C | 2 | a0002c0002t0010g0287 a0002c0009t0032g0286 |
2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1429+1625A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386390 | |||||||
| chr3:170386429 | C | T | 1 | a0002c0002t0020g0283 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1429+1664C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386429 | |||||||
| chr3:170386469 | C | G | 1 | a0009c0013t0066g0136 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1429+1704C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386469 | |||||||
| chr3:170386552 | T | G | 2 | a0001c0001t0002g0189 a0001c0001t0008g0185 |
2 | NA18950.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1429+1787T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386552 | |||||||
| chr3:170386618 | C | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1429+1853C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386618 | |||||||
| chr3:170386648 | T | C | 5 | a0002c0002t0016g0022 a0002c0002t0016g0024 a0002c0002t0016g0025 others(2): Show |
5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1429+1883T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386648 | |||||||
| chr3:170386658 | CAG | C | 11 | a0001c0001t0008g0036 a0001c0001t0008g0037 a0001c0001t0008g0051 others(8): Show |
11 | HG02486.hp1 HG02559.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1429+1894_1429+189 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386658 | |||||||
| chr3:170386842 | T | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1429+2077T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386842 | |||||||
| chr3:170386944 | A | G | 2 | a0001c0001t0002g0189 a0001c0001t0008g0185 |
2 | NA18950.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1429+2179A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170386944 | |||||||
| chr3:170387056 | C | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1429+2291C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387056 | |||||||
| chr3:170387057 | G | A | 5 | a0002c0002t0016g0022 a0002c0002t0016g0024 a0002c0002t0016g0025 others(2): Show |
5 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1429+2292G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387057 | |||||||
| chr3:170387281 | A | G | 2 | a0001c0001t0001g0137 a0009c0013t0066g0136 |
2 | HG01255.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1429+2516A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387281 | |||||||
| chr3:170387337 | T | C | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1429+2572T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387337 | |||||||
| chr3:170387349 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1429+2584C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387349 | |||||||
| chr3:170387445 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(238): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1429+2680C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387445 | |||||||
| chr3:170387504 | T | TTGCATGT others(17): Show |
1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1430-2717_1430-271 others(28): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387504 | ||||||
| chr3:170387521 | ACTT | A | 49 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0015 others(46): Show |
50 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1430-2698_1430-269 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387521 | ||||||
| chr3:170387590 | C | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1430-2633C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387590 | |||||||
| chr3:170387591 | G | A | 1 | a0002c0002t0010g0247 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1430-2632G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387591 | |||||||
| chr3:170387645 | C | T | 1 | a0001c0001t0002g0100 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1430-2578C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387645 | |||||||
| chr3:170387699 | G | A | 6 | a0002c0002t0027g0298 a0002c0002t0027g0307 a0002c0002t0049g0019 others(3): Show |
6 | HG02630.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1430-2524G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387699 | |||||||
| chr3:170387719 | C | T | 1 | a0001c0001t0072g0086 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1430-2504C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387719 | |||||||
| chr3:170387759 | T | TAA | 20 | a0002c0002t0011g0004 a0002c0002t0011g0267 a0002c0002t0011g0268 others(17): Show |
21 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1430-2450_1430-244 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387759 | ||||||
| chr3:170387759 | T | TAAAAAAA others(2): Show |
118 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0120 others(115): Show |
122 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1430-2457_1430-244 others(13): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387759 | ||||||
| chr3:170387759 | T | TAAAAAAA others(3): Show |
64 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0021 others(61): Show |
66 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1430-2458_1430-244 others(14): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387759 | ||||||
| chr3:170387759 | T | TAAAAAAA others(4): Show |
67 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(64): Show |
69 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1430-2459_1430-244 others(15): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387759 | ||||||
| chr3:170387759 | T | TAAAAAAA others(5): Show |
8 | a0002c0002t0006g0316 a0002c0002t0006g0321 a0002c0002t0006g0325 others(5): Show |
8 | HG01978.hp1 NA18949.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.1430-2460_1430-244 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387759 | ||||||
| chr3:170387760 | A | AAAAAAAA others(3): Show |
1 | a0005c0006t0001g0135 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1430-2454_1430-245 others(14): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387760 | ||||||
| chr3:170387775 | T | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(83): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1430-2448T>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387775 | |||||||
| chr3:170387851 | G | A | 1 | a0001c0001t0008g0088 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1430-2372G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387851 | |||||||
| chr3:170387859 | G | A | 2 | a0002c0002t0058g0027 a0002c0002t0059g0028 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1430-2364G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387859 | |||||||
| chr3:170387888 | C | G | 1 | a0002c0002t0025g0301 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1430-2335C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387888 | |||||||
| chr3:170387889 | C | G | 1 | a0002c0002t0025g0301 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1430-2334C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387889 | |||||||
| chr3:170387890 | C | T | 1 | a0002c0002t0025g0301 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1430-2333C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387890 | |||||||
| chr3:170387921 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1430-2302G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170387921 | |||||||
| chr3:170387933 | C | CA | 152 | a0001c0001t0001g0021 a0001c0001t0001g0179 a0001c0001t0002g0008 others(149): Show |
155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1430-2266dupA | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387933 | ||||||
| chr3:170387933 | C | CAA | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(116): Show |
125 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1430-2267_1430-226 others(6): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387933 | ||||||
| chr3:170387933 | C | CAAA | 30 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0030 others(27): Show |
30 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1430-2268_1430-226 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170387933 | ||||||
| chr3:170388111 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1430-2112C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388111 | |||||||
| chr3:170388302 | T | C | 2 | a0002c0002t0058g0027 a0002c0002t0059g0028 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1430-1921T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388302 | |||||||
| chr3:170388303 | C | G | 6 | a0001c0001t0004g0014 a0001c0001t0004g0219 a0001c0001t0004g0220 others(3): Show |
7 | NA18747.hp1 NA18942.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1430-1920C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388303 | |||||||
| chr3:170388348 | G | GGTT | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(261): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1430-1871_1430-186 others(7): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170388348 | ||||||
| chr3:170388361 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1430-1862T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388361 | |||||||
| chr3:170388526 | G | A | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1430-1697G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388526 | |||||||
| chr3:170388579 | T | G | 1 | a0001c0001t0002g0192 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1430-1644T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388579 | |||||||
| chr3:170388719 | C | T | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1430-1504C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388719 | |||||||
| chr3:170388721 | C | T | 1 | a0002c0002t0010g0287 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1430-1502C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388721 | |||||||
| chr3:170388756 | G | A | 1 | a0001c0001t0038g0152 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1430-1467G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388756 | |||||||
| chr3:170388772 | A | G | 8 | a0002c0002t0017g0299 a0002c0002t0017g0300 a0002c0002t0017g0303 others(5): Show |
8 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1430-1451A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388772 | |||||||
| chr3:170388860 | G | GTATT | 28 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(25): Show |
28 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1430-1341_1430-133 others(8): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170388860 | ||||||
| chr3:170388884 | T | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(84): Show |
91 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1430-1339T>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388884 | |||||||
| chr3:170388884 | T | TTATTTAT others(1): Show |
139 | a0001c0001t0001g0033 a0001c0001t0001g0123 a0001c0001t0001g0133 others(136): Show |
142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1430-1338_1430-133 others(12): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170388884 | ||||||
| chr3:170388884 | T | TTATTTAT others(5): Show |
13 | a0001c0001t0001g0005 a0001c0001t0001g0120 a0001c0001t0001g0121 others(10): Show |
14 | HG00438.hp2 HG00639.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1430-1338_1430-133 others(16): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170388884 | ||||||
| chr3:170388911 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1430-1312C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388911 | |||||||
| chr3:170388962 | C | T | 1 | a0008c0007t0048g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1430-1261C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170388962 | |||||||
| chr3:170389017 | G | A | 2 | a0002c0002t0058g0027 a0002c0002t0059g0028 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1430-1206G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389017 | |||||||
| chr3:170389018 | C | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0004g0056 |
3 | HG03239.hp1 HG04115.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1430-1205C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389018 | |||||||
| chr3:170389084 | G | T | 1 | a0001c0001t0001g0184 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1430-1139G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389084 | |||||||
| chr3:170389175 | G | C | 1 | a0001c0001t0004g0087 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1430-1048G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389175 | |||||||
| chr3:170389259 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0197 |
3 | NA19056.hp1 NA19057.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1430-964A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389259 | |||||||
| chr3:170389267 | C | A | 9 | a0002c0002t0011g0267 a0002c0002t0011g0268 a0002c0002t0011g0269 others(6): Show |
9 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1430-956C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389267 | |||||||
| chr3:170389316 | C | CT | 10 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0002g0103 others(7): Show |
10 | HG00642.hp2 HG02071.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1430-892dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 170389316 | ||||||
| chr3:170389400 | G | A | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1430-823G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389400 | |||||||
| chr3:170389546 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(239): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1430-677C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389546 | |||||||
| chr3:170389603 | C | T | 1 | a0001c0001t0008g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1430-620C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389603 | |||||||
| chr3:170389802 | G | C | 1 | a0001c0001t0007g0138 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1430-421G>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389802 | |||||||
| chr3:170389872 | T | C | 1 | a0001c0001t0060g0194 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1430-351T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389872 | |||||||
| chr3:170389995 | C | A | 1 | a0002c0002t0058g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1430-228C>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170389995 | |||||||
| chr3:170390068 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1430-155T>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 4/6 | chr3 | 170390068 | |||||||
| chr3:170390543 | G | T | 1 | a0002c0002t0046g0322 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1671+79G>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 5/6 | chr3 | 170390543 | |||||||
| chr3:170390696 | A | G | 1 | a0002c0002t0041g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1671+232A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 5/6 | chr3 | 170390696 | |||||||
| chr3:170390721 | C | T | 22 | a0002c0002t0006g0258 a0002c0002t0006g0312 a0002c0002t0006g0313 others(19): Show |
22 | HG00558.hp2 HG01978.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1671+257C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 5/6 | chr3 | 170390721 | |||||||
| chr3:170390778 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1672-258C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 5/6 | chr3 | 170390778 | |||||||
| chr3:170390804 | A | T | 1 | a0001c0001t0065g0094 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1672-232A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 5/6 | chr3 | 170390804 | |||||||
| chr3:170391324 | C | CT | 6 | a0001c0003t0007g0176 a0002c0002t0016g0022 a0002c0002t0016g0024 others(3): Show |
6 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1896+76dupT | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 170391324 | ||||||
| chr3:170391391 | C | T | 1 | a0002c0002t0052g0254 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1896+131C>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170391391 | |||||||
| chr3:170391481 | A | T | 1 | a0002c0002t0006g0323 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1896+221A>T | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170391481 | |||||||
| chr3:170391615 | G | A | 1 | a0008c0007t0048g0310 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1896+355G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170391615 | |||||||
| chr3:170391622 | G | A | 1 | a0001c0001t0064g0181 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1896+362G>A | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170391622 | |||||||
| chr3:170391646 | C | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(94): Show |
102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1896+386C>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170391646 | |||||||
| chr3:170391805 | A | C | 2 | a0001c0001t0068g0196 a0002c0002t0088g0309 |
2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1897-454A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170391805 | |||||||
| chr3:170391825 | TTA | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(90): Show |
97 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1897-430_1897-429d others(4): Show |
SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 170391825 | ||||||
| chr3:170391908 | A | G | 2 | a0002c0002t0027g0298 a0002c0002t0027g0307 |
2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1897-351A>G | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170391908 | |||||||
| chr3:170392223 | A | C | 2 | a0002c0002t0058g0027 a0002c0002t0059g0028 |
2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1897-36A>C | SKIL | ENSG00000136603.15 | transcript | ENST00000259119.9 | protein_coding | 6/6 | chr3 | 170392223 |