Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10152 |
| ensemblid | ENSG00000138443.17 |
| hgncid | 24011 |
| symbol | ABI2 |
| name | abl interactor 2 |
| refseq_nuc | NM_001375670.1 |
| refseq_prot | NP_001362599.1 |
| ensembl_nuc | ENST00000261018.12 |
| ensembl_prot | ENSP00000261018.9 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 203328394 |
| end | 203432169 |
| strand | + |
| ver | v1.2 |
| region | chr2:203328394-203432169 |
| region5000 | chr2:203323394-203437169 |
| regionname0 | ABI2_chr2_203328394_203432169 |
| regionname5000 | ABI2_chr2_203323394_203437169 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1626 | 318 | 78 | 60 | 140 | 10 | 28 | ABI2_chr2_203323394_203437169 | ABI2 | ATGGC others(1621): Show |
chr2 | 203323394 | 203437169 | ||
| a0001c0002 | 0/0 | 1626 | 2 | 2 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | ATGGC others(1621): Show |
chr2 | 203323394 | 203437169 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6568 | 90 | 9 | 18 | 48 | 4 | 10 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0002 | 1/0 | 6567 | 73 | 13 | 13 | 38 | 2 | 6 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6562): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0003 | 0/0 | 6568 | 38 | 13 | 16 | 3 | 2 | 4 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0004 | 0/0 | 6568 | 23 | 12 | 2 | 8 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0005 | 0/0 | 6568 | 20 | 3 | 3 | 12 | 0 | 2 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0006 | 0/0 | 6568 | 19 | 15 | 4 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0007 | 0/0 | 6572 | 6 | 0 | 0 | 6 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6567): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0008 | 0/0 | 6565 | 6 | 0 | 0 | 6 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6560): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0009 | 0/0 | 6566 | 4 | 4 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6561): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0010 | 0/0 | 6567 | 4 | 0 | 0 | 4 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6562): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0011 | 0/0 | 6568 | 3 | 3 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0012 | 0/0 | 6568 | 3 | 0 | 0 | 3 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0013 | 0/0 | 6568 | 2 | 0 | 0 | 2 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0014 | 0/0 | 6568 | 2 | 0 | 0 | 0 | 0 | 2 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0015 | 0/0 | 6567 | 2 | 0 | 1 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6562): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0016 | 0/0 | 6567 | 2 | 0 | 0 | 2 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6562): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0017 | 0/0 | 6568 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0018 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0019 | 0/0 | 6569 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6564): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0020 | 0/0 | 6568 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0021 | 0/0 | 6569 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6564): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0022 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6562): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0023 | 0/0 | 6568 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0025 | 0/0 | 6568 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0026 | 0/0 | 6568 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0027 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0028 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0029 | 0/0 | 6566 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6561): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0030 | 0/0 | 6568 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0031 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0032 | 0/0 | 6566 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6561): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0033 | 0/0 | 6568 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0034 | 0/0 | 6567 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6562): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0035 | 0/0 | 6567 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6562): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0036 | 0/0 | 6567 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6562): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0037 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6562): Show |
chr2 | 203323394 | 203437169 |
| a0001c0001t0038 | 0/0 | 6567 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6562): Show |
chr2 | 203323394 | 203437169 |
| a0001c0002t0005 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6563): Show |
chr2 | 203323394 | 203437169 |
| a0001c0002t0024 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | CCTTC others(6562): Show |
chr2 | 203323394 | 203437169 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0315 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0134 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0008g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0008g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0008g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0010g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0010g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0010g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0010g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0011g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0012g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0012g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0012g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0013g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0013g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0014g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0014g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0015g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0015g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0016g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0016g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0017g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0018g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0019g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0020g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0021g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0022g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0023g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0025g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0026g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0027g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0028g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0029g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0030g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0031g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0032g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0033g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0034g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0035g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0036g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0037g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0001t0038g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0002t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| a0001c0002t0024g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | FIN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00280 | hp2 | a0001 | c0001 | t0033 | g0092 | EUR | FIN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | FIN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0275 | EUR | FIN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00621 | hp1 | a0001 | c0001 | t0021 | g0152 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0252 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00673 | hp1 | a0001 | c0001 | t0026 | g0314 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00673 | hp2 | a0001 | c0001 | t0008 | g0035 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0169 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00738 | hp2 | a0001 | c0001 | t0020 | g0122 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0171 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0162 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0168 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0253 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0102 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0103 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0286 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01433 | hp1 | a0001 | c0001 | t0030 | g0240 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01433 | hp2 | a0001 | c0001 | t0017 | g0260 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0299 | EUR | IBS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0194 | EUR | IBS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01516 | hp1 | a0001 | c0001 | t0035 | g0064 | EUR | IBS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0193 | EUR | IBS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0174 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01884 | hp2 | a0001 | c0001 | t0022 | g0319 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0287 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0309 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0121 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0310 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01975 | hp1 | a0001 | c0001 | t0015 | g0119 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02040 | hp2 | a0001 | c0001 | t0013 | g0101 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02055 | hp2 | a0001 | c0001 | t0027 | g0117 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02080 | hp1 | a0001 | c0001 | t0029 | g0096 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02083 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0110 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0177 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0109 | EAS | CDX | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CDX | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CDX | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CDX | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02258 | hp2 | a0001 | c0001 | t0028 | g0167 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0219 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0178 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0141 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0104 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0176 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0159 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0164 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0220 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0158 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02809 | hp1 | a0001 | c0001 | t0011 | g0155 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0160 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0163 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0175 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0098 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02976 | hp2 | a0001 | c0002 | t0005 | g0116 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0173 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0166 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0154 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0140 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0170 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0179 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0149 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03688 | hp1 | a0001 | c0001 | t0025 | g0273 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0317 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0133 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0115 | SAS | BEB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03834 | hp1 | a0001 | c0001 | t0036 | g0075 | SAS | BEB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0161 | SAS | BEB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG03942 | hp2 | a0001 | c0001 | t0014 | g0281 | SAS | BEB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0311 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG04204 | hp1 | a0001 | c0001 | t0023 | g0111 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | CHB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0106 | EAS | CHB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | YRI | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | YRI | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18940 | hp1 | a0001 | c0001 | t0016 | g0086 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18946 | hp1 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18951 | hp1 | a0001 | c0001 | t0007 | g0084 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18960 | hp1 | a0001 | c0001 | t0013 | g0105 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18962 | hp2 | a0001 | c0001 | t0010 | g0067 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18968 | hp1 | a0001 | c0001 | t0012 | g0126 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18968 | hp2 | a0001 | c0001 | t0007 | g0091 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18969 | hp1 | a0001 | c0001 | t0012 | g0129 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0089 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18971 | hp2 | a0001 | c0001 | t0016 | g0088 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18978 | hp2 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18982 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18986 | hp2 | a0001 | c0001 | t0010 | g0066 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18999 | hp1 | a0001 | c0001 | t0008 | g0042 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19010 | hp2 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19030 | hp1 | a0001 | c0001 | t0018 | g0267 | AFR | LWK | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | LWK | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | LWK | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0172 | AFR | LWK | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19057 | hp1 | a0001 | c0001 | t0008 | g0036 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19066 | hp1 | a0001 | c0001 | t0010 | g0078 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19067 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19068 | hp1 | a0001 | c0001 | t0038 | g0048 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19068 | hp2 | a0001 | c0001 | t0008 | g0085 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19077 | hp1 | a0001 | c0001 | t0019 | g0147 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19081 | hp1 | a0001 | c0001 | t0007 | g0095 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19084 | hp2 | a0001 | c0001 | t0012 | g0130 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19085 | hp1 | a0001 | c0001 | t0034 | g0190 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19086 | hp2 | a0001 | c0001 | t0032 | g0034 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19087 | hp1 | a0001 | c0001 | t0010 | g0068 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19088 | hp1 | a0001 | c0001 | t0015 | g0120 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | YRI | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA19240 | hp2 | a0001 | c0001 | t0031 | g0183 | AFR | YRI | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0198 | EUR | TSI | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | TSI | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA20905 | hp1 | a0001 | c0001 | t0014 | g0278 | SAS | GIH | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | GIH | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0153 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02109 | hp2 | a0001 | c0001 | t0037 | g0320 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0099 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0180 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0165 | AFR | USA | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | USA | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA20300 | hp1 | a0001 | c0002 | t0024 | g0118 | AFR | USA | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | USA | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0315 | REF | REF | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0134 | REF | REF | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:203417014 | G | C | 1 | a0001c0002 | 2 | HG02976.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.1386G>C | p.Val462Val | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/12 | 1507/6567 | 1386/1629 | 462/542 | chr2 | 203417014 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:203328413 | C | T | 1 | a0001c0001t0038 | 1 | NA19068.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-102C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/12 | chr2 | 203328413 | |||||||
| chr2:203328436 | C | G | 1 | a0001c0001t0037 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/12 | 79 | chr2 | 203328436 | ||||||
| chr2:203427382 | G | A | 1 | a0001c0001t0017 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*30G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 30 | chr2 | 203427382 | ||||||
| chr2:203427794 | T | C | 24 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(21): Show |
181 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*442T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 442 | chr2 | 203427794 | ||||||
| chr2:203428187 | T | C | 1 | a0001c0001t0018 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*835T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 835 | chr2 | 203428187 | ||||||
| chr2:203428373 | G | A | 1 | a0001c0001t0016 | 2 | NA18940.hp1 NA18971.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1021G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 1021 | chr2 | 203428373 | ||||||
| chr2:203428422 | T | G | 1 | a0001c0001t0013 | 2 | HG02040.hp2 NA18960.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1070T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 1070 | chr2 | 203428422 | ||||||
| chr2:203428582 | T | C | 2 | a0001c0001t0010 a0001c0001t0029 |
5 | HG02080.hp1 NA18962.hp2 NA18986.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1230T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 1230 | chr2 | 203428582 | ||||||
| chr2:203428846 | C | T | 1 | a0001c0001t0028 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1494C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 1494 | chr2 | 203428846 | ||||||
| chr2:203429341 | C | T | 1 | a0001c0001t0027 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1989C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 1989 | chr2 | 203429341 | ||||||
| chr2:203429380 | G | C | 1 | a0001c0001t0011 | 3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2028G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2028 | chr2 | 203429380 | ||||||
| chr2:203429518 | G | A | 1 | a0001c0001t0012 | 3 | NA18968.hp1 NA18969.hp1 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2166G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2166 | chr2 | 203429518 | ||||||
| chr2:203429561 | A | G | 1 | a0001c0001t0036 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2209A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2209 | chr2 | 203429561 | ||||||
| chr2:203429689 | A | G | 24 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(21): Show |
181 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*2337A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2337 | chr2 | 203429689 | ||||||
| chr2:203429753 | C | CA | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(21): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*2418dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2419 | INFO_REALIGN_3_PRIME | chr2 | 203429753 | |||||
| chr2:203429753 | C | CAA | 5 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0019 others(2): Show |
29 | HG00621.hp1 HG00738.hp2 HG01943.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2417_*2418dupAA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2419 | INFO_REALIGN_3_PRIME | chr2 | 203429753 | |||||
| chr2:203429870 | C | A | 1 | a0001c0001t0011 | 3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2518C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2518 | chr2 | 203429870 | ||||||
| chr2:203429885 | G | A | 1 | a0001c0001t0022 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2533G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2533 | chr2 | 203429885 | ||||||
| chr2:203429886 | C | G | 1 | a0001c0001t0022 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2534C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2534 | chr2 | 203429886 | ||||||
| chr2:203430144 | G | C | 1 | a0001c0001t0035 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2792G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2792 | chr2 | 203430144 | ||||||
| chr2:203430169 | A | G | 2 | a0001c0001t0006 a0001c0001t0028 |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2817A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2817 | chr2 | 203430169 | ||||||
| chr2:203430425 | T | C | 1 | a0001c0001t0022 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3073T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 3073 | chr2 | 203430425 | ||||||
| chr2:203430501 | C | T | 1 | a0001c0001t0026 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3149C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 3149 | chr2 | 203430501 | ||||||
| chr2:203430551 | G | A | 1 | a0001c0001t0030 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3199G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 3199 | chr2 | 203430551 | ||||||
| chr2:203430727 | G | A | 1 | a0001c0001t0014 | 2 | HG03942.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3375G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 3375 | chr2 | 203430727 | ||||||
| chr2:203430818 | G | A | 1 | a0001c0001t0022 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3466G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 3466 | chr2 | 203430818 | ||||||
| chr2:203430937 | C | A | 1 | a0001c0001t0031 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3585C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 3585 | chr2 | 203430937 | ||||||
| chr2:203430964 | C | T | 1 | a0001c0001t0025 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3612C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 3612 | chr2 | 203430964 | ||||||
| chr2:203431568 | G | GAGCAC | 1 | a0001c0001t0007 | 6 | NA18951.hp1 NA18968.hp2 NA18971.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4226_*4230dupCAGC others(1): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 4231 | INFO_REALIGN_3_PRIME | chr2 | 203431568 | |||||
| chr2:203431688 | A | G | 8 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0013 others(5): Show |
30 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*4336A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 4336 | chr2 | 203431688 | ||||||
| chr2:203431696 | TA | T | 10 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0012 others(7): Show |
38 | HG00738.hp2 HG01884.hp2 HG01943.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*4356delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 4356 | INFO_REALIGN_3_PRIME | chr2 | 203431696 | |||||
| chr2:203431793 | A | G | 1 | a0001c0001t0033 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4441A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 4441 | chr2 | 203431793 | ||||||
| chr2:203431822 | A | C | 1 | a0001c0001t0020 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4470A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 4470 | chr2 | 203431822 | ||||||
| chr2:203431847 | G | A | 1 | a0001c0001t0023 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4495G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 4495 | chr2 | 203431847 | ||||||
| chr2:203432022 | GGA | G | 2 | a0001c0001t0008 a0001c0001t0032 |
7 | HG00673.hp2 NA18946.hp1 NA18982.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4672_*4673delAG | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 4672 | INFO_REALIGN_3_PRIME | chr2 | 203432022 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:203328753 | G | C | 1 | a0001c0001t0006g0001 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.117+122G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203328753 | |||||||
| chr2:203328895 | T | TCGGCCGC others(3): Show |
1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+267_117+276dup others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203328895 | ||||||
| chr2:203328926 | G | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.117+295G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203328926 | |||||||
| chr2:203328965 | T | G | 96 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(93): Show |
96 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.117+334T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203328965 | |||||||
| chr2:203328983 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.117+352C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203328983 | |||||||
| chr2:203329026 | C | T | 1 | a0001c0001t0003g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117+395C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329026 | |||||||
| chr2:203329314 | AAT | A | 137 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(134): Show |
137 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.117+684_117+685del others(2): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329314 | |||||||
| chr2:203329341 | A | AT | 193 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(190): Show |
193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.117+734dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203329341 | ||||||
| chr2:203329341 | A | ATT | 35 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(32): Show |
35 | HG00280.hp2 HG00673.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.117+733_117+734dup others(2): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203329341 | ||||||
| chr2:203329341 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0002g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.117+725_117+734del others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203329341 | ||||||
| chr2:203329434 | G | A | 1 | a0001c0001t0006g0001 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.117+803G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329434 | |||||||
| chr2:203329470 | A | G | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.117+839A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329470 | |||||||
| chr2:203329621 | G | T | 1 | a0001c0001t0002g0097 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.117+990G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329621 | |||||||
| chr2:203329695 | T | C | 24 | a0001c0001t0005g0098 a0001c0001t0005g0099 a0001c0001t0005g0100 others(21): Show |
24 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.117+1064T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329695 | |||||||
| chr2:203329808 | C | G | 23 | a0001c0001t0005g0100 a0001c0001t0005g0102 a0001c0001t0005g0103 others(20): Show |
23 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+1177C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329808 | |||||||
| chr2:203329957 | G | C | 1 | a0001c0001t0002g0008 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.117+1326G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329957 | |||||||
| chr2:203329959 | A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+1328A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329959 | |||||||
| chr2:203329971 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.117+1340A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329971 | |||||||
| chr2:203330095 | C | G | 1 | a0001c0001t0006g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.117+1464C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203330095 | |||||||
| chr2:203330205 | TGACCC | T | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117+1577_117+1581d others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203330205 | ||||||
| chr2:203330361 | A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+1730A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203330361 | |||||||
| chr2:203330392 | CA | C | 260 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(257): Show |
260 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.117+1780delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203330392 | ||||||
| chr2:203330392 | CAA | C | 16 | a0001c0001t0001g0207 a0001c0001t0001g0299 a0001c0001t0001g0300 others(13): Show |
16 | HG01167.hp2 HG01515.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.117+1779_117+1780d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203330392 | ||||||
| chr2:203330759 | G | C | 1 | a0001c0001t0001g0216 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.117+2128G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203330759 | |||||||
| chr2:203330869 | A | G | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+2238A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203330869 | |||||||
| chr2:203330940 | T | G | 188 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(185): Show |
188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.117+2309T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203330940 | |||||||
| chr2:203331005 | T | TAAAGCAT others(159): Show |
1 | a0001c0001t0002g0014 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.117+2386_117+2387i others(168): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203331005 | ||||||
| chr2:203331180 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.117+2549T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203331180 | |||||||
| chr2:203331348 | C | CTTTTTT | 60 | a0001c0001t0001g0186 a0001c0001t0001g0207 a0001c0001t0001g0218 others(57): Show |
60 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.117+2732_117+2737d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203331348 | ||||||
| chr2:203331348 | C | CTTTTTTT | 192 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(189): Show |
192 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.117+2731_117+2737d others(9): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203331348 | ||||||
| chr2:203331348 | C | CTTTTTTT others(1): Show |
32 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(29): Show |
32 | HG00597.hp1 HG00621.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.117+2730_117+2737d others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203331348 | ||||||
| chr2:203331560 | T | C | 1 | a0001c0001t0001g0292 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.117+2929T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203331560 | |||||||
| chr2:203331560 | T | G | 17 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.117+2929T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203331560 | |||||||
| chr2:203331701 | G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+3070G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203331701 | |||||||
| chr2:203331808 | CT | C | 11 | a0001c0001t0001g0182 a0001c0001t0001g0290 a0001c0001t0001g0291 others(8): Show |
11 | HG00642.hp1 HG01975.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.117+3196delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203331808 | ||||||
| chr2:203331808 | CTT | C | 173 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0200 others(170): Show |
173 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.117+3195_117+3196d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203331808 | ||||||
| chr2:203331895 | C | T | 7 | a0001c0001t0002g0195 a0001c0001t0002g0197 a0001c0001t0002g0198 others(4): Show |
7 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+3264C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203331895 | |||||||
| chr2:203332020 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.117+3389G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203332020 | |||||||
| chr2:203332241 | A | G | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | NA18980.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.117+3610A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203332241 | |||||||
| chr2:203332493 | C | T | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+3862C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203332493 | |||||||
| chr2:203332657 | T | G | 1 | a0001c0001t0015g0120 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.117+4026T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203332657 | |||||||
| chr2:203332768 | G | A | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+4137G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203332768 | |||||||
| chr2:203333149 | A | G | 1 | a0001c0001t0004g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.117+4518A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203333149 | |||||||
| chr2:203333580 | T | G | 96 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(93): Show |
96 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.117+4949T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203333580 | |||||||
| chr2:203333938 | T | C | 1 | a0001c0001t0002g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.117+5307T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203333938 | |||||||
| chr2:203333947 | T | C | 95 | a0001c0001t0001g0182 a0001c0001t0001g0200 a0001c0001t0001g0201 others(92): Show |
95 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.117+5316T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203333947 | |||||||
| chr2:203334190 | C | G | 2 | a0001c0001t0003g0191 a0001c0001t0003g0192 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.117+5559C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203334190 | |||||||
| chr2:203334230 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.117+5599C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203334230 | |||||||
| chr2:203334280 | A | G | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.117+5649A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203334280 | |||||||
| chr2:203334536 | A | C | 5 | a0001c0001t0010g0066 a0001c0001t0010g0067 a0001c0001t0010g0068 others(2): Show |
5 | HG02080.hp1 NA18962.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+5905A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203334536 | |||||||
| chr2:203334668 | A | AT | 178 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(175): Show |
178 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.117+6051dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203334668 | ||||||
| chr2:203334668 | A | ATT | 9 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0284 others(6): Show |
9 | HG00735.hp2 HG00741.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.117+6050_117+6051d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203334668 | ||||||
| chr2:203334854 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.117+6223T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203334854 | |||||||
| chr2:203334877 | T | C | 95 | a0001c0001t0001g0182 a0001c0001t0001g0200 a0001c0001t0001g0201 others(92): Show |
95 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.117+6246T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203334877 | |||||||
| chr2:203334982 | T | C | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.117+6351T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203334982 | |||||||
| chr2:203335040 | G | A | 16 | a0001c0001t0001g0200 a0001c0001t0001g0228 a0001c0001t0001g0229 others(13): Show |
16 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.117+6409G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335040 | |||||||
| chr2:203335055 | T | C | 1 | a0001c0001t0030g0240 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.117+6424T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335055 | |||||||
| chr2:203335136 | T | A | 1 | a0001c0001t0003g0286 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.117+6505T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335136 | |||||||
| chr2:203335471 | C | G | 188 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(185): Show |
188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.117+6840C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335471 | |||||||
| chr2:203335550 | G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+6919G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335550 | |||||||
| chr2:203335555 | G | T | 16 | a0001c0001t0001g0200 a0001c0001t0001g0228 a0001c0001t0001g0229 others(13): Show |
16 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.117+6924G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335555 | |||||||
| chr2:203335592 | A | C | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+6961A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335592 | |||||||
| chr2:203335644 | T | C | 6 | a0001c0001t0005g0102 a0001c0001t0005g0103 a0001c0001t0005g0104 others(3): Show |
6 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+7013T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335644 | |||||||
| chr2:203335966 | A | T | 1 | a0001c0001t0010g0078 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.117+7335A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335966 | |||||||
| chr2:203336050 | A | G | 3 | a0001c0001t0011g0153 a0001c0001t0011g0154 a0001c0001t0011g0155 |
3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.117+7419A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336050 | |||||||
| chr2:203336122 | T | G | 1 | a0001c0001t0003g0286 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.117+7491T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336122 | |||||||
| chr2:203336250 | G | A | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.117+7619G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336250 | |||||||
| chr2:203336319 | A | C | 301 | a0001c0001t0001g0138 a0001c0001t0001g0181 a0001c0001t0001g0182 others(298): Show |
301 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.117+7688A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336319 | |||||||
| chr2:203336342 | A | G | 95 | a0001c0001t0001g0182 a0001c0001t0001g0200 a0001c0001t0001g0201 others(92): Show |
95 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.117+7711A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336342 | |||||||
| chr2:203336546 | A | C | 1 | a0001c0001t0034g0190 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.117+7915A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336546 | |||||||
| chr2:203336560 | A | G | 301 | a0001c0001t0001g0138 a0001c0001t0001g0181 a0001c0001t0001g0182 others(298): Show |
301 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.117+7929A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336560 | |||||||
| chr2:203336600 | T | A | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+7969T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336600 | |||||||
| chr2:203336601 | A | G | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+7970A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336601 | |||||||
| chr2:203336832 | G | C | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.117+8201G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336832 | |||||||
| chr2:203336845 | G | A | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117+8214G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336845 | |||||||
| chr2:203336986 | G | A | 1 | a0001c0001t0002g0083 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.117+8355G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336986 | |||||||
| chr2:203337541 | A | T | 1 | a0001c0001t0001g0283 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.117+8910A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337541 | |||||||
| chr2:203337746 | A | G | 1 | a0001c0001t0010g0068 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.117+9115A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337746 | |||||||
| chr2:203337899 | A | C | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9268A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337899 | |||||||
| chr2:203337900 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9269C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337900 | |||||||
| chr2:203337902 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9271C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337902 | |||||||
| chr2:203337903 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9272G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337903 | |||||||
| chr2:203337905 | C | A | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9274C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337905 | |||||||
| chr2:203337907 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9276G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337907 | |||||||
| chr2:203337908 | T | G | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9277T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337908 | |||||||
| chr2:203337909 | A | T | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9278A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337909 | |||||||
| chr2:203337911 | T | A | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9280T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337911 | |||||||
| chr2:203337912 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9281C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337912 | |||||||
| chr2:203337913 | C | G | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9282C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337913 | |||||||
| chr2:203337914 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9283C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337914 | |||||||
| chr2:203337915 | A | T | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9284A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337915 | |||||||
| chr2:203337945 | G | T | 1 | a0001c0001t0003g0225 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.117+9314G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337945 | |||||||
| chr2:203338069 | T | A | 2 | a0001c0001t0003g0203 a0001c0001t0034g0190 |
2 | HG00438.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.117+9438T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338069 | |||||||
| chr2:203338070 | A | G | 1 | a0001c0001t0035g0064 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.117+9439A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338070 | |||||||
| chr2:203338115 | G | C | 188 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(185): Show |
188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.117+9484G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338115 | |||||||
| chr2:203338315 | G | C | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.117+9684G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338315 | |||||||
| chr2:203338444 | G | T | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+9813G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338444 | |||||||
| chr2:203338453 | G | C | 2 | a0001c0001t0004g0121 a0001c0001t0020g0122 |
2 | HG00738.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.117+9822G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338453 | |||||||
| chr2:203338840 | T | A | 1 | a0001c0001t0003g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117+10209T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338840 | |||||||
| chr2:203338920 | GTGTGTGT others(3): Show |
G | 8 | a0001c0001t0005g0100 a0001c0001t0005g0110 a0001c0001t0005g0151 others(5): Show |
8 | HG02109.hp1 HG02135.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+10291_117+1030 others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | ||||||
| chr2:203338920 | GTGTGTGT others(17): Show |
G | 2 | a0001c0001t0005g0109 a0001c0002t0005g0116 |
2 | HG02155.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.117+10291_117+1031 others(28): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | ||||||
| chr2:203338920 | GTGTGTGT others(19): Show |
G | 1 | a0001c0001t0005g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.117+10291_117+1031 others(30): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | ||||||
| chr2:203338920 | GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0005g0108 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.117+10291_117+1031 others(32): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | ||||||
| chr2:203338920 | GTGTGTGT others(23): Show |
G | 4 | a0001c0001t0005g0104 a0001c0001t0005g0106 a0001c0001t0005g0107 others(1): Show |
4 | HG02293.hp2 NA18747.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+10291_117+1032 others(34): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | ||||||
| chr2:203338920 | GTGTGTGT others(27): Show |
G | 2 | a0001c0001t0005g0102 a0001c0001t0005g0103 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.117+10291_117+1032 others(38): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | ||||||
| chr2:203338920 | GTGTGTGT others(29): Show |
G | 1 | a0001c0001t0013g0101 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.117+10291_117+1032 others(40): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | ||||||
| chr2:203338920 | GTGTGTGT others(41): Show |
G | 3 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0021g0152 |
3 | HG00621.hp1 NA18992.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.117+10291_117+1033 others(52): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | ||||||
| chr2:203338920 | GTGTGTGT others(43): Show |
G | 1 | a0001c0001t0005g0112 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.117+10291_117+1034 others(54): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | ||||||
| chr2:203338921 | TGTGTGTG others(35): Show |
T | 1 | a0001c0002t0024g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.117+10291_117+1033 others(46): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338921 | |||||||
| chr2:203338922 | GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+10293_117+1032 others(32): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338922 | ||||||
| chr2:203338922 | GTGTGTGT others(23): Show |
G | 1 | a0001c0001t0005g0156 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.117+10293_117+1032 others(34): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338922 | ||||||
| chr2:203338924 | GTGTGTAT others(13): Show |
G | 1 | a0001c0001t0003g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.117+10295_117+1031 others(24): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338924 | ||||||
| chr2:203338924 | GTGTGTAT others(15): Show |
G | 1 | a0001c0001t0003g0185 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.117+10295_117+1031 others(26): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338924 | ||||||
| chr2:203338924 | GTGTGTAT others(29): Show |
G | 1 | a0001c0001t0031g0183 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.117+10295_117+1033 others(40): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338924 | ||||||
| chr2:203338926 | GTGTATAT others(11): Show |
G | 1 | a0001c0001t0003g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.117+10297_117+1031 others(22): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338926 | GTGTATAT others(13): Show |
G | 1 | a0001c0001t0003g0209 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.117+10297_117+1031 others(24): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338926 | GTGTATAT others(17): Show |
G | 1 | a0001c0001t0003g0199 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.117+10297_117+1032 others(28): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338926 | GTGTATAT others(19): Show |
G | 2 | a0001c0001t0003g0221 a0001c0001t0003g0286 |
2 | HG01358.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.117+10297_117+1032 others(30): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338926 | GTGTATAT others(21): Show |
G | 4 | a0001c0001t0003g0192 a0001c0001t0003g0222 a0001c0001t0003g0309 others(1): Show |
4 | HG01928.hp1 HG01952.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+10297_117+1032 others(32): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338926 | GTGTATAT others(23): Show |
G | 3 | a0001c0001t0003g0188 a0001c0001t0003g0191 a0001c0001t0003g0287 |
3 | HG01891.hp2 HG02896.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.117+10297_117+1032 others(34): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338926 | GTGTATAT others(25): Show |
G | 3 | a0001c0001t0003g0189 a0001c0001t0003g0204 a0001c0001t0003g0208 |
3 | HG01074.hp1 HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.117+10297_117+1032 others(36): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338926 | GTGTATAT others(27): Show |
G | 6 | a0001c0001t0003g0206 a0001c0001t0003g0210 a0001c0001t0003g0211 others(3): Show |
6 | HG01167.hp2 HG01255.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+10297_117+1033 others(38): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338926 | GTGTATAT others(31): Show |
G | 9 | a0001c0001t0001g0186 a0001c0001t0001g0218 a0001c0001t0001g0259 others(6): Show |
9 | HG00735.hp2 HG03453.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+10297_117+1033 others(42): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338926 | GTGTATAT others(33): Show |
G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0270 a0001c0001t0001g0285 others(2): Show |
5 | HG01109.hp2 HG01516.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+10297_117+1033 others(44): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338926 | GTGTATAT others(35): Show |
G | 12 | a0001c0001t0001g0230 a0001c0001t0001g0247 a0001c0001t0001g0277 others(9): Show |
12 | HG00673.hp1 HG00738.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.117+10297_117+1033 others(46): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338926 | GTGTATAT others(37): Show |
G | 29 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0207 others(26): Show |
29 | HG00438.hp1 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.117+10297_117+1034 others(48): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338926 | GTGTATAT others(39): Show |
G | 34 | a0001c0001t0001g0202 a0001c0001t0001g0212 a0001c0001t0001g0213 others(31): Show |
34 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.117+10297_117+1034 others(50): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338926 | GTGTATAT others(41): Show |
G | 7 | a0001c0001t0001g0227 a0001c0001t0001g0234 a0001c0001t0001g0251 others(4): Show |
7 | HG00423.hp1 HG01175.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+10297_117+1034 others(52): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338926 | GTGTATAT others(43): Show |
G | 1 | a0001c0001t0001g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.117+10297_117+1034 others(54): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | ||||||
| chr2:203338927 | TGTATATG others(29): Show |
T | 5 | a0001c0001t0001g0283 a0001c0001t0002g0187 a0001c0001t0003g0220 others(2): Show |
5 | HG02055.hp1 HG02698.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+10297_117+1033 others(40): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338927 | |||||||
| chr2:203338928 | GTATATGT others(31): Show |
G | 2 | a0001c0001t0003g0253 a0001c0001t0030g0240 |
2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.117+10303_117+1034 others(42): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338928 | ||||||
| chr2:203338928 | GTATATGT others(33): Show |
G | 1 | a0001c0001t0003g0252 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.117+10303_117+1034 others(44): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338928 | ||||||
| chr2:203338928 | GTATATGT others(35): Show |
G | 1 | a0001c0001t0001g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.117+10303_117+1034 others(46): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338928 | ||||||
| chr2:203338928 | GTATATGT others(37): Show |
G | 4 | a0001c0001t0001g0264 a0001c0001t0001g0276 a0001c0001t0001g0292 others(1): Show |
4 | HG01081.hp2 NA18978.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+10303_117+1034 others(48): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338928 | ||||||
| chr2:203338928 | GTATATGT others(39): Show |
G | 3 | a0001c0001t0001g0258 a0001c0001t0001g0294 a0001c0001t0001g0313 |
3 | HG04115.hp1 HG04228.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.117+10303_117+1034 others(50): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338928 | ||||||
| chr2:203338930 | A | G | 24 | a0001c0001t0004g0135 a0001c0001t0005g0098 a0001c0001t0005g0099 others(21): Show |
24 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.117+10299A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338930 | |||||||
| chr2:203338932 | A | G | 25 | a0001c0001t0001g0224 a0001c0001t0004g0135 a0001c0001t0005g0098 others(22): Show |
25 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.117+10301A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338932 | |||||||
| chr2:203338934 | GTA | G | 3 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0157 |
3 | HG02523.hp1 NA18966.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.117+10330_117+1033 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338934 | ||||||
| chr2:203338934 | GTATATAT others(43): Show |
G | 1 | a0001c0001t0002g0077 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.117+10328_117+1037 others(54): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338934 | ||||||
| chr2:203338935 | T | TATATATA others(19): Show |
1 | a0001c0001t0004g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.117+10329_117+1033 others(30): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338935 | ||||||
| chr2:203338936 | A | G | 119 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(116): Show |
119 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.117+10305A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338936 | |||||||
| chr2:203338938 | A | G | 24 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0005g0098 others(21): Show |
24 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.117+10307A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338938 | |||||||
| chr2:203338939 | TATATATA others(37): Show |
T | 3 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0080 |
3 | HG02145.hp1 HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.117+10332_117+1037 others(48): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338939 | ||||||
| chr2:203338940 | A | G | 24 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0004g0148 others(21): Show |
24 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.117+10309A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338940 | |||||||
| chr2:203338941 | T | TATATATA others(33): Show |
1 | a0001c0001t0004g0131 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.117+10329_117+1033 others(44): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338941 | ||||||
| chr2:203338942 | A | G | 23 | a0001c0001t0002g0047 a0001c0001t0004g0148 a0001c0001t0005g0098 others(20): Show |
23 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.117+10311A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338942 | |||||||
| chr2:203338943 | T | TATATATA others(7): Show |
3 | a0001c0001t0004g0142 a0001c0001t0004g0144 a0001c0001t0004g0145 |
3 | HG02559.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.117+10325_117+1032 others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338943 | ||||||
| chr2:203338943 | T | TATATATA others(31): Show |
1 | a0001c0001t0012g0126 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.117+10327_117+1032 others(42): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338943 | ||||||
| chr2:203338943 | TATATATA others(13): Show |
T | 10 | a0001c0001t0002g0040 a0001c0001t0002g0044 a0001c0001t0002g0093 others(7): Show |
10 | HG01168.hp2 HG01169.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.117+10352_117+1037 others(24): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338943 | ||||||
| chr2:203338944 | A | G | 15 | a0001c0001t0005g0098 a0001c0001t0006g0001 a0001c0001t0006g0149 others(12): Show |
15 | HG00733.hp2 HG01109.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.117+10313A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338944 | |||||||
| chr2:203338945 | T | TATATATA others(65): Show |
1 | a0001c0001t0004g0143 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.117+10325_117+1032 others(76): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338945 | ||||||
| chr2:203338945 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0138 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.117+10327_117+1032 others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338945 | ||||||
| chr2:203338945 | T | TATATATA others(9): Show |
1 | a0001c0001t0004g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.117+10329_117+1033 others(20): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338945 | ||||||
| chr2:203338945 | TATATATA others(11): Show |
T | 8 | a0001c0001t0002g0016 a0001c0001t0002g0020 a0001c0001t0002g0059 others(5): Show |
8 | HG00280.hp2 HG00423.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+10332_117+1034 others(22): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338945 | ||||||
| chr2:203338946 | A | G | 9 | a0001c0001t0006g0001 a0001c0001t0006g0169 a0001c0001t0006g0170 others(6): Show |
9 | HG00733.hp2 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.117+10315A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338946 | |||||||
| chr2:203338947 | TATATATA others(9): Show |
T | 15 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0023 others(12): Show |
15 | HG00597.hp2 HG00673.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.117+10332_117+1034 others(20): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338947 | ||||||
| chr2:203338947 | TATATATA others(29): Show |
T | 1 | a0001c0001t0002g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.117+10332_117+1036 others(40): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338947 | ||||||
| chr2:203338948 | A | G | 4 | a0001c0001t0005g0109 a0001c0001t0006g0170 a0001c0001t0006g0174 others(1): Show |
4 | HG01884.hp1 HG02155.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+10317A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338948 | |||||||
| chr2:203338949 | T | TATATATA others(23): Show |
1 | a0001c0001t0020g0122 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.117+10329_117+1033 others(34): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338949 | ||||||
| chr2:203338949 | TATATATA others(7): Show |
T | 18 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(15): Show |
18 | HG01884.hp1 HG02486.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.117+10332_117+1034 others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338949 | ||||||
| chr2:203338949 | TATATATA others(27): Show |
T | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.117+10332_117+1036 others(38): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338949 | ||||||
| chr2:203338950 | A | G | 2 | a0001c0001t0005g0115 a0001c0001t0006g0170 |
2 | HG03225.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.117+10319A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338950 | |||||||
| chr2:203338951 | T | TATATATA others(21): Show |
1 | a0001c0001t0004g0141 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.117+10327_117+1032 others(32): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338951 | ||||||
| chr2:203338951 | T | TATATATA others(43): Show |
1 | a0001c0001t0004g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.117+10327_117+1032 others(54): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338951 | ||||||
| chr2:203338951 | TATATATA others(5): Show |
T | 23 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0018 others(20): Show |
23 | HG00741.hp1 HG01975.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+10332_117+1034 others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338951 | ||||||
| chr2:203338952 | A | G | 2 | a0001c0001t0005g0108 a0001c0001t0006g0170 |
2 | HG03225.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.117+10321A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338952 | |||||||
| chr2:203338953 | T | TATATAAA others(91): Show |
1 | a0001c0001t0015g0119 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.117+10327_117+1032 others(102): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338953 | ||||||
| chr2:203338953 | T | TATATATA others(27): Show |
1 | a0001c0001t0004g0136 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.117+10329_117+1033 others(38): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338953 | ||||||
| chr2:203338953 | T | TATATATA others(35): Show |
1 | a0001c0001t0004g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.117+10331_117+1033 others(46): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338953 | ||||||
| chr2:203338953 | TATATATA others(3): Show |
T | 12 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0014 others(9): Show |
12 | HG00323.hp1 HG02040.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+10332_117+1034 others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338953 | ||||||
| chr2:203338953 | TATATATA others(23): Show |
T | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.117+10332_117+1036 others(34): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338953 | ||||||
| chr2:203338954 | A | G | 2 | a0001c0001t0005g0106 a0001c0001t0005g0107 |
2 | NA18747.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.117+10323A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338954 | |||||||
| chr2:203338955 | T | TATATATA others(81): Show |
1 | a0001c0001t0004g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.117+10331_117+1033 others(92): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338955 | ||||||
| chr2:203338955 | TATATATA others(1): Show |
T | 12 | a0001c0001t0002g0008 a0001c0001t0002g0021 a0001c0001t0002g0025 others(9): Show |
12 | HG01081.hp1 HG01256.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+10332_117+1033 others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338955 | ||||||
| chr2:203338955 | TATATATA others(21): Show |
T | 2 | a0001c0001t0002g0031 a0001c0001t0003g0079 |
2 | HG01175.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.117+10332_117+1035 others(32): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338955 | ||||||
| chr2:203338957 | TATATAA | T | 5 | a0001c0001t0002g0019 a0001c0001t0002g0063 a0001c0001t0003g0073 others(2): Show |
5 | HG01192.hp2 HG02148.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+10332_117+1033 others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338957 | ||||||
| chr2:203338957 | TATATAAA others(19): Show |
T | 5 | a0001c0001t0002g0039 a0001c0001t0002g0043 a0001c0001t0002g0058 others(2): Show |
5 | HG00609.hp2 HG01361.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+10332_117+1035 others(30): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338957 | ||||||
| chr2:203338959 | T | A | 1 | a0001c0001t0004g0132 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.117+10328T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338959 | |||||||
| chr2:203338959 | TATAA | T | 3 | a0001c0001t0002g0030 a0001c0001t0002g0050 a0001c0001t0002g0056 |
3 | HG01943.hp2 HG02523.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.117+10332_117+1033 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338959 | ||||||
| chr2:203338959 | TATAAATA others(17): Show |
T | 2 | a0001c0001t0006g0149 a0001c0001t0006g0164 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.117+10332_117+1035 others(28): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338959 | ||||||
| chr2:203338961 | T | A | 4 | a0001c0001t0004g0125 a0001c0001t0004g0128 a0001c0001t0012g0129 others(1): Show |
4 | NA18747.hp1 NA18969.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+10330T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338961 | |||||||
| chr2:203338961 | TAAATATA others(15): Show |
T | 2 | a0001c0001t0006g0170 a0001c0001t0006g0172 |
2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.117+10332_117+1035 others(26): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338961 | ||||||
| chr2:203338963 | A | T | 60 | a0001c0001t0002g0017 a0001c0001t0002g0051 a0001c0001t0002g0071 others(57): Show |
60 | HG00621.hp2 HG00642.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.117+10332A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338963 | |||||||
| chr2:203338964 | A | G | 12 | a0001c0001t0006g0001 a0001c0001t0006g0150 a0001c0001t0006g0162 others(9): Show |
12 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+10333A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338964 | |||||||
| chr2:203338966 | A | G | 7 | a0001c0001t0006g0150 a0001c0001t0006g0163 a0001c0001t0006g0165 others(4): Show |
7 | HG01884.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+10335A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338966 | |||||||
| chr2:203338968 | A | G | 6 | a0001c0001t0006g0150 a0001c0001t0006g0163 a0001c0001t0006g0165 others(3): Show |
6 | HG01884.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+10337A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338968 | |||||||
| chr2:203338969 | T | A | 2 | a0001c0001t0004g0141 a0001c0001t0020g0122 |
2 | HG00738.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.117+10338T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338969 | |||||||
| chr2:203338970 | A | G | 3 | a0001c0001t0006g0165 a0001c0001t0006g0166 a0001c0001t0006g0179 |
3 | HG03130.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.117+10339A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338970 | |||||||
| chr2:203338971 | T | A | 1 | a0001c0001t0004g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.117+10340T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338971 | |||||||
| chr2:203338971 | T | TATATATA others(55): Show |
1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.117+10351_117+1035 others(66): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338971 | ||||||
| chr2:203338972 | A | G | 4 | a0001c0001t0001g0182 a0001c0001t0005g0113 a0001c0001t0005g0114 others(1): Show |
4 | HG00621.hp1 HG02622.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+10341A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338972 | |||||||
| chr2:203338973 | T | A | 1 | a0001c0001t0004g0127 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.117+10342T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338973 | |||||||
| chr2:203338974 | A | G | 2 | a0001c0001t0001g0308 a0001c0001t0005g0112 |
2 | HG02083.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.117+10343A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338974 | |||||||
| chr2:203338975 | T | A | 5 | a0001c0001t0004g0136 a0001c0001t0004g0137 a0001c0001t0004g0139 others(2): Show |
5 | HG01975.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+10344T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338975 | |||||||
| chr2:203338977 | T | A | 1 | a0001c0001t0004g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.117+10346T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338977 | |||||||
| chr2:203338983 | A | AATATATA others(5): Show |
1 | a0001c0001t0004g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.117+10366_117+1037 others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | ||||||
| chr2:203338983 | A | AATATATA others(7): Show |
1 | a0001c0001t0004g0145 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.117+10364_117+1037 others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | ||||||
| chr2:203338983 | A | AATATATA others(19): Show |
1 | a0001c0001t0004g0125 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.117+10369_117+1037 others(30): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | ||||||
| chr2:203338983 | A | AATATATA others(39): Show |
1 | a0001c0001t0004g0124 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.117+10371_117+1037 others(50): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | ||||||
| chr2:203338983 | A | AATATATA others(59): Show |
1 | a0001c0001t0015g0120 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.117+10371_117+1037 others(70): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | ||||||
| chr2:203338983 | A | AATATATA others(99): Show |
1 | a0001c0001t0004g0157 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.117+10371_117+1037 others(110): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | ||||||
| chr2:203338983 | A | AATATATA others(41): Show |
3 | a0001c0001t0004g0128 a0001c0001t0012g0129 a0001c0001t0012g0130 |
3 | NA18969.hp1 NA19064.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.117+10371_117+1037 others(52): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | ||||||
| chr2:203338983 | A | AATATATA others(47): Show |
1 | a0001c0001t0004g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.117+10373_117+1037 others(58): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | ||||||
| chr2:203338983 | A | AATATATA others(65): Show |
1 | a0001c0001t0004g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.117+10373_117+1037 others(76): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | ||||||
| chr2:203338983 | A | T | 286 | a0001c0001t0001g0138 a0001c0001t0001g0181 a0001c0001t0001g0182 others(283): Show |
286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.117+10352A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338983 | |||||||
| chr2:203338986 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.117+10355A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338986 | |||||||
| chr2:203338993 | TATATATA others(8): Show |
T | 1 | a0001c0001t0002g0017 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.117+10364_117+1037 others(19): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338993 | ||||||
| chr2:203339007 | T | A | 3 | a0001c0001t0011g0153 a0001c0001t0011g0154 a0001c0001t0011g0155 |
3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.117+10376T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339007 | |||||||
| chr2:203339037 | A | C | 1 | a0001c0001t0002g0059 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.117+10406A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339037 | |||||||
| chr2:203339095 | G | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG00280.hp1 HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.117+10464G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339095 | |||||||
| chr2:203339126 | A | G | 1 | a0001c0001t0003g0289 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.117+10495A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339126 | |||||||
| chr2:203339233 | G | A | 2 | a0001c0002t0005g0116 a0001c0002t0024g0118 |
2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.117+10602G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339233 | |||||||
| chr2:203339567 | C | G | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.117+10936C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339567 | |||||||
| chr2:203339592 | A | G | 23 | a0001c0001t0005g0081 a0001c0001t0005g0100 a0001c0001t0005g0102 others(20): Show |
23 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+10961A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339592 | |||||||
| chr2:203339593 | A | G | 1 | a0001c0001t0006g0171 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.117+10962A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339593 | |||||||
| chr2:203339912 | C | T | 1 | a0001c0001t0010g0068 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.117+11281C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339912 | |||||||
| chr2:203339986 | A | T | 1 | a0001c0001t0003g0199 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.117+11355A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339986 | |||||||
| chr2:203340235 | G | GTGGGGAG others(3): Show |
1 | a0001c0001t0002g0018 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.117+11613_117+1162 others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203340235 | ||||||
| chr2:203340284 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.117+11653T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340284 | |||||||
| chr2:203340328 | A | G | 1 | a0001c0001t0002g0058 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.117+11697A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340328 | |||||||
| chr2:203340371 | A | AT | 25 | a0001c0001t0001g0239 a0001c0001t0002g0057 a0001c0001t0002g0076 others(22): Show |
25 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.117+11753dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203340371 | ||||||
| chr2:203340393 | G | A | 4 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+11762G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340393 | |||||||
| chr2:203340425 | G | A | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+11794G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340425 | |||||||
| chr2:203340435 | C | T | 1 | a0001c0001t0004g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.117+11804C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340435 | |||||||
| chr2:203340497 | G | T | 1 | a0001c0001t0002g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.117+11866G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340497 | |||||||
| chr2:203340526 | A | G | 1 | a0001c0001t0004g0145 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.117+11895A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340526 | |||||||
| chr2:203340531 | T | C | 10 | a0001c0001t0001g0138 a0001c0001t0004g0136 a0001c0001t0004g0137 others(7): Show |
10 | HG02293.hp1 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.117+11900T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340531 | |||||||
| chr2:203340546 | C | T | 1 | a0001c0001t0005g0081 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.117+11915C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340546 | |||||||
| chr2:203340547 | G | A | 3 | a0001c0001t0003g0184 a0001c0001t0003g0185 a0001c0001t0031g0183 |
3 | HG01891.hp1 HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.117+11916G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340547 | |||||||
| chr2:203340745 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0014g0281 |
2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.117+12114C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340745 | |||||||
| chr2:203340824 | G | GA | 10 | a0001c0001t0001g0243 a0001c0001t0002g0019 a0001c0001t0003g0191 others(7): Show |
10 | HG01192.hp2 HG01257.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.117+12203dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203340824 | ||||||
| chr2:203340860 | T | C | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.117+12229T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340860 | |||||||
| chr2:203341060 | C | T | 1 | a0001c0001t0004g0145 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.117+12429C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203341060 | |||||||
| chr2:203341359 | G | A | 4 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+12728G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203341359 | |||||||
| chr2:203341443 | A | G | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.117+12812A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203341443 | |||||||
| chr2:203341485 | C | A | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+12854C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203341485 | |||||||
| chr2:203341535 | C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.117+12904C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203341535 | |||||||
| chr2:203341718 | A | C | 2 | a0001c0001t0001g0280 a0001c0001t0001g0292 |
2 | NA18978.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.117+13087A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203341718 | |||||||
| chr2:203342255 | A | C | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+13624A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203342255 | |||||||
| chr2:203342552 | T | TTTTA | 59 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0214 others(56): Show |
59 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.117+13961_117+1396 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203342552 | ||||||
| chr2:203342552 | T | TTTTATTT others(1): Show |
85 | a0001c0001t0001g0138 a0001c0001t0001g0202 a0001c0001t0001g0207 others(82): Show |
85 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.117+13957_117+1396 others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203342552 | ||||||
| chr2:203342552 | T | TTTTATTT others(5): Show |
25 | a0001c0001t0001g0182 a0001c0001t0001g0200 a0001c0001t0001g0201 others(22): Show |
25 | HG00423.hp1 HG00642.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.117+13953_117+1396 others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203342552 | ||||||
| chr2:203342552 | TTTTATTT others(1): Show |
T | 6 | a0001c0001t0002g0014 a0001c0001t0002g0056 a0001c0001t0003g0210 others(3): Show |
6 | HG02055.hp2 HG02155.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+13957_117+1396 others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203342552 | ||||||
| chr2:203342552 | TTTTATTT others(5): Show |
T | 2 | a0001c0001t0003g0317 a0001c0001t0037g0320 |
2 | HG02109.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.117+13953_117+1396 others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203342552 | ||||||
| chr2:203342570 | T | TTATTTAT others(5): Show |
1 | a0001c0001t0001g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.117+13950_117+1395 others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203342570 | ||||||
| chr2:203342679 | A | G | 2 | a0001c0001t0003g0203 a0001c0001t0034g0190 |
2 | HG00438.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.117+14048A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203342679 | |||||||
| chr2:203342704 | T | C | 7 | a0001c0001t0001g0201 a0001c0001t0001g0245 a0001c0001t0001g0246 others(4): Show |
7 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+14073T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203342704 | |||||||
| chr2:203342733 | C | T | 1 | a0001c0001t0006g0170 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.117+14102C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203342733 | |||||||
| chr2:203342847 | C | CA | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.117+14217dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203342847 | ||||||
| chr2:203342860 | T | C | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+14229T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203342860 | |||||||
| chr2:203343083 | G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+14452G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203343083 | |||||||
| chr2:203343256 | C | T | 1 | a0001c0001t0003g0189 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.117+14625C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203343256 | |||||||
| chr2:203343278 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.117+14647C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203343278 | |||||||
| chr2:203343310 | G | C | 3 | a0001c0001t0003g0184 a0001c0001t0003g0185 a0001c0001t0031g0183 |
3 | HG01891.hp1 HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.117+14679G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203343310 | |||||||
| chr2:203343381 | A | G | 186 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(183): Show |
186 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.117+14750A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203343381 | |||||||
| chr2:203343959 | C | A | 4 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+15328C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203343959 | |||||||
| chr2:203344043 | G | C | 184 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(181): Show |
184 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.117+15412G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344043 | |||||||
| chr2:203344062 | T | C | 1 | a0001c0002t0005g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.117+15431T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344062 | |||||||
| chr2:203344192 | A | T | 3 | a0001c0001t0003g0252 a0001c0001t0003g0253 a0001c0001t0030g0240 |
3 | HG00642.hp2 HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.117+15561A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344192 | |||||||
| chr2:203344361 | A | AT | 21 | a0001c0001t0005g0081 a0001c0001t0005g0100 a0001c0001t0005g0102 others(18): Show |
21 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.117+15739dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203344361 | ||||||
| chr2:203344512 | A | C | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.117+15881A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344512 | |||||||
| chr2:203344540 | T | TTTG | 8 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0097 others(5): Show |
8 | HG01081.hp1 HG02080.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+15930_117+1593 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203344540 | ||||||
| chr2:203344540 | TTTG | T | 3 | a0001c0001t0022g0319 a0001c0001t0025g0273 a0001c0001t0037g0320 |
3 | HG01884.hp2 HG02109.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.117+15930_117+1593 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203344540 | ||||||
| chr2:203344562 | T | TTG | 91 | a0001c0001t0001g0238 a0001c0001t0002g0002 a0001c0001t0002g0005 others(88): Show |
91 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.117+15932_117+1593 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203344562 | ||||||
| chr2:203344564 | T | G | 10 | a0001c0001t0001g0138 a0001c0001t0004g0136 a0001c0001t0004g0137 others(7): Show |
10 | HG02293.hp1 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.117+15933T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344564 | |||||||
| chr2:203344567 | G | T | 91 | a0001c0001t0001g0238 a0001c0001t0002g0002 a0001c0001t0002g0005 others(88): Show |
91 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.117+15936G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344567 | |||||||
| chr2:203344567 | GT | G | 207 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(204): Show |
207 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.117+15948delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203344567 | ||||||
| chr2:203344568 | T | G | 91 | a0001c0001t0001g0238 a0001c0001t0002g0002 a0001c0001t0002g0005 others(88): Show |
91 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.117+15937T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344568 | |||||||
| chr2:203344568 | T | TTTTTG | 15 | a0001c0001t0001g0138 a0001c0001t0004g0136 a0001c0001t0004g0137 others(12): Show |
15 | HG02080.hp1 HG02293.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.117+15941_117+1594 others(9): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203344568 | ||||||
| chr2:203344574 | T | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+15943T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344574 | |||||||
| chr2:203344637 | G | A | 3 | a0001c0001t0003g0252 a0001c0001t0003g0253 a0001c0001t0030g0240 |
3 | HG00642.hp2 HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.117+16006G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344637 | |||||||
| chr2:203344815 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0308 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.117+16184C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344815 | |||||||
| chr2:203344918 | CGCTCTGT others(17): Show |
C | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+16331_117+1635 others(28): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203344918 | ||||||
| chr2:203344970 | C | G | 2 | a0001c0001t0001g0216 a0001c0001t0001g0241 |
2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.117+16339C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344970 | |||||||
| chr2:203345101 | C | T | 1 | a0001c0001t0004g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.117+16470C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345101 | |||||||
| chr2:203345199 | C | T | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+16568C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345199 | |||||||
| chr2:203345367 | C | G | 21 | a0001c0001t0005g0081 a0001c0001t0005g0100 a0001c0001t0005g0102 others(18): Show |
21 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.117+16736C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345367 | |||||||
| chr2:203345575 | A | G | 1 | a0001c0002t0005g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.117+16944A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345575 | |||||||
| chr2:203345683 | A | T | 1 | a0001c0001t0001g0216 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.117+17052A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345683 | |||||||
| chr2:203345743 | A | G | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.117+17112A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345743 | |||||||
| chr2:203345963 | T | A | 1 | a0001c0001t0002g0020 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.117+17332T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345963 | |||||||
| chr2:203345969 | C | T | 1 | a0001c0001t0001g0305 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.117+17338C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345969 | |||||||
| chr2:203346023 | T | C | 1 | a0001c0001t0004g0145 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.117+17392T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203346023 | |||||||
| chr2:203346438 | A | C | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.117+17807A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203346438 | |||||||
| chr2:203346445 | C | T | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.117+17814C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203346445 | |||||||
| chr2:203346509 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.117+17878G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203346509 | |||||||
| chr2:203346535 | G | C | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+17904G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203346535 | |||||||
| chr2:203346643 | T | C | 2 | a0001c0001t0003g0191 a0001c0001t0003g0192 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.117+18012T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203346643 | |||||||
| chr2:203346754 | T | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.117+18123T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203346754 | |||||||
| chr2:203347033 | A | G | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117+18402A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203347033 | |||||||
| chr2:203347163 | G | T | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117+18532G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203347163 | |||||||
| chr2:203347235 | T | G | 3 | a0001c0001t0011g0153 a0001c0001t0011g0154 a0001c0001t0011g0155 |
3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.117+18604T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203347235 | |||||||
| chr2:203347558 | C | G | 4 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+18927C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203347558 | |||||||
| chr2:203347768 | A | G | 186 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(183): Show |
186 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.118-19109A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203347768 | |||||||
| chr2:203348045 | A | T | 1 | a0001c0001t0003g0194 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.118-18832A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348045 | |||||||
| chr2:203348109 | C | T | 1 | a0001c0001t0004g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.118-18768C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348109 | |||||||
| chr2:203348184 | T | C | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.118-18693T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348184 | |||||||
| chr2:203348257 | A | T | 1 | a0001c0001t0036g0075 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.118-18620A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348257 | |||||||
| chr2:203348496 | A | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-18381A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348496 | |||||||
| chr2:203348510 | G | A | 1 | a0001c0001t0003g0203 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.118-18367G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348510 | |||||||
| chr2:203348584 | A | G | 3 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 |
3 | HG02451.hp2 HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.118-18293A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348584 | |||||||
| chr2:203348591 | T | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0295 a0001c0001t0004g0217 |
3 | HG00597.hp1 NA19057.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.118-18286T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348591 | |||||||
| chr2:203348757 | C | T | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.118-18120C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348757 | |||||||
| chr2:203348780 | T | C | 289 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(286): Show |
289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.118-18097T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348780 | |||||||
| chr2:203348862 | T | A | 1 | a0001c0001t0002g0062 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.118-18015T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348862 | |||||||
| chr2:203348920 | T | G | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.118-17957T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348920 | |||||||
| chr2:203348920 | TTTTG | T | 4 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0080 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-17933_118-1793 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203348920 | ||||||
| chr2:203349045 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.118-17832G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349045 | |||||||
| chr2:203349053 | C | T | 1 | a0001c0001t0015g0119 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.118-17824C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349053 | |||||||
| chr2:203349228 | C | T | 1 | a0001c0001t0014g0278 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.118-17649C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349228 | |||||||
| chr2:203349554 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.118-17323G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349554 | |||||||
| chr2:203349647 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.118-17230C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349647 | |||||||
| chr2:203349669 | T | C | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.118-17208T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349669 | |||||||
| chr2:203349738 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.118-17139A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349738 | |||||||
| chr2:203349955 | C | T | 1 | a0001c0001t0003g0311 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.118-16922C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349955 | |||||||
| chr2:203350003 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.118-16874C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350003 | |||||||
| chr2:203350044 | T | C | 3 | a0001c0001t0001g0279 a0001c0001t0001g0295 a0001c0001t0004g0217 |
3 | HG00597.hp1 NA19057.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.118-16833T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350044 | |||||||
| chr2:203350195 | A | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0246 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.118-16682A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350195 | |||||||
| chr2:203350237 | C | T | 2 | a0001c0001t0002g0017 a0001c0001t0002g0053 |
2 | NA18952.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.118-16640C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350237 | |||||||
| chr2:203350248 | C | T | 7 | a0001c0001t0001g0207 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | NA18940.hp2 NA18946.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-16629C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350248 | |||||||
| chr2:203350303 | T | C | 188 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(185): Show |
188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.118-16574T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350303 | |||||||
| chr2:203350509 | G | C | 188 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(185): Show |
188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.118-16368G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350509 | |||||||
| chr2:203350540 | CT | C | 23 | a0001c0001t0001g0214 a0001c0001t0001g0247 a0001c0001t0001g0270 others(20): Show |
23 | HG01167.hp2 HG01168.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.118-16321delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203350540 | ||||||
| chr2:203350662 | C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-16215C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350662 | |||||||
| chr2:203350688 | C | A | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.118-16189C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350688 | |||||||
| chr2:203350698 | C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-16179C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350698 | |||||||
| chr2:203350759 | C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-16118C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350759 | |||||||
| chr2:203350790 | G | A | 6 | a0001c0001t0001g0229 a0001c0001t0001g0235 a0001c0001t0001g0236 others(3): Show |
6 | HG00438.hp2 HG00609.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-16087G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350790 | |||||||
| chr2:203350862 | T | TTG | 14 | a0001c0001t0001g0138 a0001c0001t0001g0251 a0001c0001t0004g0121 others(11): Show |
14 | HG00738.hp2 HG01943.hp1 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-15986_118-1598 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203350862 | ||||||
| chr2:203350862 | T | TTGTG | 3 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 |
3 | HG02451.hp2 HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.118-15988_118-1598 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203350862 | ||||||
| chr2:203350862 | TTG | T | 107 | a0001c0001t0001g0216 a0001c0001t0001g0255 a0001c0001t0001g0256 others(104): Show |
107 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.118-15986_118-1598 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203350862 | ||||||
| chr2:203350862 | TTGTG | T | 4 | a0001c0001t0003g0184 a0001c0001t0003g0185 a0001c0001t0006g0149 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-15988_118-1598 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203350862 | ||||||
| chr2:203350889 | TGTGC | T | 33 | a0001c0001t0001g0181 a0001c0001t0001g0224 a0001c0001t0002g0187 others(30): Show |
33 | HG00438.hp1 HG00621.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.118-15986_118-1598 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203350889 | ||||||
| chr2:203350891 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.118-15986T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350891 | |||||||
| chr2:203350891 | TGC | T | 108 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(105): Show |
108 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.118-15977_118-1597 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203350891 | ||||||
| chr2:203350893 | C | T | 14 | a0001c0001t0001g0231 a0001c0001t0001g0251 a0001c0001t0001g0274 others(11): Show |
14 | HG01255.hp1 HG01257.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-15984C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350893 | |||||||
| chr2:203350895 | C | T | 7 | a0001c0001t0001g0218 a0001c0001t0001g0243 a0001c0001t0001g0279 others(4): Show |
7 | HG00597.hp1 HG00673.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-15982C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350895 | |||||||
| chr2:203350905 | C | A | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.118-15972C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350905 | |||||||
| chr2:203350959 | T | G | 4 | a0001c0001t0006g0149 a0001c0001t0006g0164 a0001c0001t0006g0173 others(1): Show |
4 | HG02572.hp2 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-15918T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350959 | |||||||
| chr2:203350964 | C | A | 1 | a0001c0001t0001g0248 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.118-15913C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350964 | |||||||
| chr2:203351201 | A | G | 1 | a0001c0001t0002g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.118-15676A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351201 | |||||||
| chr2:203351318 | A | G | 1 | a0001c0001t0002g0198 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.118-15559A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351318 | |||||||
| chr2:203351459 | T | G | 1 | a0001c0001t0008g0022 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.118-15418T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351459 | |||||||
| chr2:203351532 | G | GT | 176 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(173): Show |
176 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.118-15330dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203351532 | ||||||
| chr2:203351532 | G | GTT | 13 | a0001c0001t0001g0216 a0001c0001t0001g0295 a0001c0001t0001g0316 others(10): Show |
13 | HG00597.hp1 HG00733.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.118-15331_118-1533 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203351532 | ||||||
| chr2:203351657 | T | C | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.118-15220T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351657 | |||||||
| chr2:203351755 | C | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0308 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.118-15122C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351755 | |||||||
| chr2:203351798 | A | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.118-15079A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351798 | |||||||
| chr2:203351836 | G | A | 301 | a0001c0001t0001g0138 a0001c0001t0001g0181 a0001c0001t0001g0182 others(298): Show |
301 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.118-15041G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351836 | |||||||
| chr2:203351942 | A | G | 1 | a0001c0001t0003g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.118-14935A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351942 | |||||||
| chr2:203351972 | G | A | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.118-14905G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351972 | |||||||
| chr2:203352067 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.118-14810G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203352067 | |||||||
| chr2:203352256 | T | A | 1 | a0001c0001t0014g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.118-14621T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203352256 | |||||||
| chr2:203352569 | GA | G | 95 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(92): Show |
95 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.118-14298delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203352569 | ||||||
| chr2:203353087 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.118-13790A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353087 | |||||||
| chr2:203353208 | T | G | 1 | a0001c0001t0001g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-13669T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353208 | |||||||
| chr2:203353296 | A | C | 1 | a0001c0001t0002g0052 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.118-13581A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353296 | |||||||
| chr2:203353434 | A | AC | 7 | a0001c0001t0001g0258 a0001c0001t0002g0002 a0001c0001t0002g0070 others(4): Show |
7 | HG02027.hp1 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-13439dupC | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203353434 | ||||||
| chr2:203353698 | A | C | 1 | a0001c0001t0003g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.118-13179A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353698 | |||||||
| chr2:203353699 | T | C | 1 | a0001c0001t0002g0023 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.118-13178T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353699 | |||||||
| chr2:203353737 | G | A | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.118-13140G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353737 | |||||||
| chr2:203353752 | C | T | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.118-13125C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353752 | |||||||
| chr2:203353813 | C | T | 1 | a0001c0001t0003g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.118-13064C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353813 | |||||||
| chr2:203354100 | G | A | 1 | a0001c0001t0015g0119 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.118-12777G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354100 | |||||||
| chr2:203354125 | A | G | 1 | a0001c0001t0002g0093 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.118-12752A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354125 | |||||||
| chr2:203354150 | A | G | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.118-12727A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354150 | |||||||
| chr2:203354345 | A | G | 1 | a0001c0001t0006g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.118-12532A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354345 | |||||||
| chr2:203354509 | G | C | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.118-12368G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354509 | |||||||
| chr2:203354705 | TAAG | T | 39 | a0001c0001t0002g0187 a0001c0001t0002g0195 a0001c0001t0002g0197 others(36): Show |
39 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.118-12167_118-1216 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203354705 | ||||||
| chr2:203354803 | A | C | 1 | a0001c0001t0002g0059 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.118-12074A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354803 | |||||||
| chr2:203354839 | A | T | 1 | a0001c0001t0001g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.118-12038A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354839 | |||||||
| chr2:203354957 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.118-11920T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354957 | |||||||
| chr2:203355181 | C | G | 1 | a0001c0001t0002g0007 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.118-11696C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355181 | |||||||
| chr2:203355205 | A | G | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.118-11672A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355205 | |||||||
| chr2:203355703 | C | T | 289 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(286): Show |
289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.118-11174C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355703 | |||||||
| chr2:203355704 | G | A | 4 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-11173G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355704 | |||||||
| chr2:203355828 | T | G | 1 | a0001c0001t0001g0247 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.118-11049T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355828 | |||||||
| chr2:203355828 | TC | T | 17 | a0001c0001t0005g0100 a0001c0001t0005g0102 a0001c0001t0005g0103 others(14): Show |
17 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.118-11048delC | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355828 | |||||||
| chr2:203355829 | C | A | 2 | a0001c0001t0005g0114 a0001c0001t0005g0115 |
2 | HG03831.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.118-11048C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355829 | |||||||
| chr2:203355829 | C | CA | 26 | a0001c0001t0002g0016 a0001c0001t0002g0027 a0001c0001t0002g0039 others(23): Show |
26 | HG00738.hp2 HG01361.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.118-11026dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203355829 | ||||||
| chr2:203355829 | C | CAA | 7 | a0001c0001t0006g0168 a0001c0001t0006g0171 a0001c0001t0006g0172 others(4): Show |
7 | HG01109.hp1 HG01169.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-11027_118-1102 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203355829 | ||||||
| chr2:203355829 | C | CAAA | 11 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(8): Show |
11 | HG01168.hp2 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.118-11028_118-1102 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203355829 | ||||||
| chr2:203355829 | CA | C | 76 | a0001c0001t0001g0182 a0001c0001t0001g0200 a0001c0001t0001g0201 others(73): Show |
76 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.118-11026delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203355829 | ||||||
| chr2:203355830 | A | AAAACTGT others(3): Show |
1 | a0001c0001t0001g0247 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.118-11044_118-1104 others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203355830 | ||||||
| chr2:203355880 | G | A | 1 | a0001c0001t0004g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.118-10997G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355880 | |||||||
| chr2:203355926 | T | C | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0208 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-10951T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355926 | |||||||
| chr2:203355936 | A | G | 1 | a0001c0001t0002g0055 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.118-10941A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355936 | |||||||
| chr2:203356052 | T | C | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.118-10825T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203356052 | |||||||
| chr2:203356478 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.118-10399C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203356478 | |||||||
| chr2:203356510 | A | G | 1 | a0001c0001t0033g0092 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.118-10367A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203356510 | |||||||
| chr2:203356514 | G | A | 1 | a0001c0001t0002g0010 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.118-10363G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203356514 | |||||||
| chr2:203356515 | C | A | 1 | a0001c0001t0021g0152 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.118-10362C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203356515 | |||||||
| chr2:203356613 | A | T | 16 | a0001c0001t0001g0200 a0001c0001t0001g0228 a0001c0001t0001g0229 others(13): Show |
16 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.118-10264A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203356613 | |||||||
| chr2:203356638 | A | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0292 |
2 | NA18978.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.118-10239A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203356638 | |||||||
| chr2:203356848 | AT | A | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.118-10016delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203356848 | ||||||
| chr2:203357043 | ATTT | A | 94 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(91): Show |
94 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.118-9831_118-9829d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203357043 | ||||||
| chr2:203357100 | T | A | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.118-9777T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203357100 | |||||||
| chr2:203357287 | T | A | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.118-9590T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203357287 | |||||||
| chr2:203357542 | C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-9335C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203357542 | |||||||
| chr2:203357644 | G | T | 1 | a0001c0001t0008g0085 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.118-9233G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203357644 | |||||||
| chr2:203357720 | G | T | 1 | a0001c0001t0003g0287 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.118-9157G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203357720 | |||||||
| chr2:203357757 | T | G | 1 | a0001c0001t0001g0271 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.118-9120T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203357757 | |||||||
| chr2:203357759 | T | TTTTG | 3 | a0001c0001t0002g0063 a0001c0001t0004g0139 a0001c0001t0004g0140 |
3 | HG02723.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.118-9093_118-9090d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203357759 | ||||||
| chr2:203357759 | TTTTGTTT others(1): Show |
T | 186 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(183): Show |
186 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.118-9097_118-9090d others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203357759 | ||||||
| chr2:203358017 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.118-8860C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358017 | |||||||
| chr2:203358071 | T | G | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.118-8806T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358071 | |||||||
| chr2:203358071 | T | TGTGTG | 3 | a0001c0001t0001g0182 a0001c0001t0001g0294 a0001c0001t0011g0154 |
3 | HG02622.hp2 HG03139.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.118-8806_118-8805i others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358071 | |||||||
| chr2:203358071 | T | TTG | 64 | a0001c0001t0001g0224 a0001c0001t0001g0261 a0001c0001t0001g0275 others(61): Show |
64 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.118-8764_118-8763d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | ||||||
| chr2:203358071 | T | TTGTG | 24 | a0001c0001t0002g0010 a0001c0001t0002g0014 a0001c0001t0002g0032 others(21): Show |
24 | HG01074.hp2 HG01175.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.118-8766_118-8763d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | ||||||
| chr2:203358071 | T | TTGTGTG | 22 | a0001c0001t0001g0138 a0001c0001t0002g0002 a0001c0001t0002g0027 others(19): Show |
22 | HG01257.hp1 HG01258.hp1 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.118-8768_118-8763d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | ||||||
| chr2:203358071 | T | TTGTGTGT others(1): Show |
12 | a0001c0001t0002g0024 a0001c0001t0002g0026 a0001c0001t0002g0029 others(9): Show |
12 | HG02040.hp2 HG02155.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.118-8770_118-8763d others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | ||||||
| chr2:203358071 | T | TTGTGTGT others(3): Show |
8 | a0001c0001t0002g0028 a0001c0001t0004g0127 a0001c0001t0004g0148 others(5): Show |
8 | HG03098.hp2 HG03195.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-8772_118-8763d others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | ||||||
| chr2:203358071 | T | TTGTGTGT others(5): Show |
10 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0003g0210 others(7): Show |
10 | HG00621.hp1 HG02083.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.118-8774_118-8763d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | ||||||
| chr2:203358071 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0002g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.118-8776_118-8763d others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | ||||||
| chr2:203358071 | TTG | T | 80 | a0001c0001t0001g0186 a0001c0001t0001g0200 a0001c0001t0001g0201 others(77): Show |
80 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.118-8764_118-8763d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | ||||||
| chr2:203358071 | TTGTG | T | 9 | a0001c0001t0001g0238 a0001c0001t0001g0306 a0001c0001t0002g0005 others(6): Show |
9 | HG00423.hp2 HG01175.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.118-8766_118-8763d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | ||||||
| chr2:203358071 | TTGTGTG | T | 20 | a0001c0001t0001g0254 a0001c0001t0001g0277 a0001c0001t0004g0142 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.118-8768_118-8763d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | ||||||
| chr2:203358107 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0003g0188 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.118-8766_118-8755d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358107 | ||||||
| chr2:203358109 | GTGTGTT | G | 14 | a0001c0001t0003g0199 a0001c0001t0003g0219 a0001c0001t0003g0221 others(11): Show |
14 | HG00642.hp1 HG00642.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-8764_118-8759d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358109 | ||||||
| chr2:203358109 | GTGTGTTT others(3): Show |
G | 8 | a0001c0001t0002g0187 a0001c0001t0002g0195 a0001c0001t0002g0197 others(5): Show |
8 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-8764_118-8755d others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358109 | ||||||
| chr2:203358111 | GTGTT | G | 3 | a0001c0001t0003g0189 a0001c0001t0003g0223 a0001c0001t0003g0311 |
3 | HG01074.hp1 HG03710.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.118-8748_118-8745d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358111 | ||||||
| chr2:203358113 | GTT | G | 3 | a0001c0001t0003g0309 a0001c0001t0005g0176 a0001c0002t0024g0118 |
3 | HG01928.hp1 HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.118-8762_118-8761d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358113 | ||||||
| chr2:203358115 | T | G | 25 | a0001c0001t0001g0294 a0001c0001t0003g0191 a0001c0001t0003g0192 others(22): Show |
25 | HG00738.hp2 HG01884.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.118-8762T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358115 | |||||||
| chr2:203358119 | T | G | 1 | a0001c0001t0003g0226 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.118-8758T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358119 | |||||||
| chr2:203358180 | T | G | 3 | a0001c0001t0002g0057 a0001c0001t0002g0070 a0001c0001t0002g0076 |
3 | NA18970.hp1 NA18991.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.118-8697T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358180 | |||||||
| chr2:203358234 | A | G | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0208 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-8643A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358234 | |||||||
| chr2:203358322 | A | G | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.118-8555A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358322 | |||||||
| chr2:203358466 | A | C | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-8411A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358466 | |||||||
| chr2:203358482 | C | T | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.118-8395C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358482 | |||||||
| chr2:203358789 | C | T | 4 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-8088C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358789 | |||||||
| chr2:203359162 | A | G | 4 | a0001c0001t0006g0165 a0001c0001t0006g0166 a0001c0001t0006g0174 others(1): Show |
4 | HG01884.hp1 HG03130.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-7715A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203359162 | |||||||
| chr2:203359845 | TG | T | 184 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(181): Show |
184 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.118-7023delG | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203359845 | ||||||
| chr2:203359957 | C | T | 2 | a0001c0001t0004g0139 a0001c0001t0004g0140 |
2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.118-6920C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203359957 | |||||||
| chr2:203359981 | T | C | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-6896T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203359981 | |||||||
| chr2:203360013 | C | G | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.118-6864C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360013 | |||||||
| chr2:203360138 | T | C | 3 | a0001c0001t0003g0184 a0001c0001t0003g0185 a0001c0001t0031g0183 |
3 | HG01891.hp1 HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.118-6739T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360138 | |||||||
| chr2:203360184 | C | CA | 8 | a0001c0001t0002g0023 a0001c0001t0002g0060 a0001c0001t0002g0061 others(5): Show |
8 | HG02145.hp1 HG02145.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-6670dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203360184 | ||||||
| chr2:203360184 | CA | C | 182 | a0001c0001t0001g0138 a0001c0001t0001g0181 a0001c0001t0001g0182 others(179): Show |
182 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.118-6670delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203360184 | ||||||
| chr2:203360186 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.118-6691A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360186 | |||||||
| chr2:203360205 | A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-6672A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360205 | |||||||
| chr2:203360377 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.118-6500A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360377 | |||||||
| chr2:203360383 | G | A | 1 | a0001c0001t0005g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.118-6494G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360383 | |||||||
| chr2:203360596 | A | C | 1 | a0001c0001t0004g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.118-6281A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360596 | |||||||
| chr2:203360882 | C | A | 1 | a0001c0001t0002g0097 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.118-5995C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360882 | |||||||
| chr2:203361280 | G | T | 42 | a0001c0001t0002g0187 a0001c0001t0002g0195 a0001c0001t0002g0197 others(39): Show |
42 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.118-5597G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203361280 | |||||||
| chr2:203361339 | C | T | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.118-5538C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203361339 | |||||||
| chr2:203361608 | A | G | 42 | a0001c0001t0002g0187 a0001c0001t0002g0195 a0001c0001t0002g0197 others(39): Show |
42 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.118-5269A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203361608 | |||||||
| chr2:203361827 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.118-5050C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203361827 | |||||||
| chr2:203362154 | T | C | 1 | a0001c0001t0002g0097 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.118-4723T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203362154 | |||||||
| chr2:203362720 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118-4157T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203362720 | |||||||
| chr2:203362721 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118-4156T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203362721 | |||||||
| chr2:203362724 | T | G | 1 | a0001c0001t0001g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118-4153T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203362724 | |||||||
| chr2:203362744 | C | G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0224 a0001c0001t0001g0277 |
3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.118-4133C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203362744 | |||||||
| chr2:203362967 | A | G | 3 | a0001c0001t0002g0021 a0001c0001t0002g0023 a0001c0001t0002g0049 |
3 | HG03491.hp2 HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.118-3910A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203362967 | |||||||
| chr2:203362996 | A | G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0224 a0001c0001t0001g0277 |
3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.118-3881A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203362996 | |||||||
| chr2:203363202 | G | A | 1 | a0001c0001t0006g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.118-3675G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363202 | |||||||
| chr2:203363334 | G | A | 4 | a0001c0001t0004g0136 a0001c0001t0004g0137 a0001c0001t0004g0139 others(1): Show |
4 | HG02630.hp1 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-3543G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363334 | |||||||
| chr2:203363377 | C | G | 1 | a0001c0001t0004g0141 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.118-3500C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363377 | |||||||
| chr2:203363402 | T | C | 1 | a0001c0001t0003g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.118-3475T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363402 | |||||||
| chr2:203363525 | C | T | 3 | a0001c0001t0011g0153 a0001c0001t0011g0154 a0001c0001t0011g0155 |
3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.118-3352C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363525 | |||||||
| chr2:203363578 | T | C | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.118-3299T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363578 | |||||||
| chr2:203363787 | A | G | 1 | a0001c0001t0003g0189 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.118-3090A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363787 | |||||||
| chr2:203363859 | G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-3018G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363859 | |||||||
| chr2:203364043 | C | T | 1 | a0001c0001t0004g0124 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.118-2834C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203364043 | |||||||
| chr2:203364091 | C | CT | 19 | a0001c0001t0001g0272 a0001c0001t0006g0001 a0001c0001t0006g0149 others(16): Show |
19 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.118-2772dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203364091 | ||||||
| chr2:203364091 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0080 |
3 | HG02145.hp1 HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.118-2781_118-2772d others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203364091 | ||||||
| chr2:203364318 | TCCTGACC others(16): Show |
T | 1 | a0001c0001t0035g0064 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.118-2555_118-2533d others(25): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203364318 | ||||||
| chr2:203364474 | A | G | 1 | a0001c0002t0024g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.118-2403A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203364474 | |||||||
| chr2:203364491 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.118-2386G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203364491 | |||||||
| chr2:203364734 | AT | A | 28 | a0001c0001t0001g0259 a0001c0001t0001g0270 a0001c0001t0003g0184 others(25): Show |
28 | HG01074.hp1 HG01255.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.118-2128delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203364734 | ||||||
| chr2:203364749 | T | C | 95 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(92): Show |
95 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.118-2128T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203364749 | |||||||
| chr2:203365089 | A | G | 2 | a0001c0002t0005g0116 a0001c0002t0024g0118 |
2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.118-1788A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203365089 | |||||||
| chr2:203365224 | A | T | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.118-1653A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203365224 | |||||||
| chr2:203365267 | T | C | 1 | a0001c0001t0002g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.118-1610T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203365267 | |||||||
| chr2:203365527 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.118-1350T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203365527 | |||||||
| chr2:203365536 | T | A | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.118-1341T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203365536 | |||||||
| chr2:203365572 | T | C | 3 | a0001c0001t0001g0138 a0001c0001t0004g0141 a0001c0001t0004g0145 |
3 | HG02293.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.118-1305T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203365572 | |||||||
| chr2:203365622 | C | CT | 100 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(97): Show |
100 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.118-1230dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203365622 | ||||||
| chr2:203365622 | C | CTT | 20 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0046 others(17): Show |
20 | HG01109.hp1 HG01168.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.118-1231_118-1230d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203365622 | ||||||
| chr2:203365622 | CT | C | 124 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0200 others(121): Show |
124 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.118-1230delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203365622 | ||||||
| chr2:203365622 | CTT | C | 6 | a0001c0001t0001g0202 a0001c0001t0001g0207 a0001c0001t0001g0299 others(3): Show |
6 | HG01496.hp2 HG01515.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-1231_118-1230d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203365622 | ||||||
| chr2:203365622 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0004g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.118-1240_118-1230d others(13): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203365622 | ||||||
| chr2:203365622 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0011g0153 a0001c0001t0011g0154 a0001c0001t0011g0155 |
3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.118-1241_118-1230d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203365622 | ||||||
| chr2:203365966 | A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-911A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203365966 | |||||||
| chr2:203365974 | CTTTGTTT others(3): Show |
C | 1 | a0001c0001t0003g0193 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.118-895_118-886del others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203365974 | ||||||
| chr2:203366055 | G | A | 1 | a0001c0001t0003g0225 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.118-822G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203366055 | |||||||
| chr2:203366406 | AT | A | 7 | a0001c0001t0001g0207 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | NA18940.hp2 NA18946.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-462delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203366406 | ||||||
| chr2:203366682 | T | C | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.118-195T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203366682 | |||||||
| chr2:203366692 | A | G | 1 | a0001c0001t0003g0253 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.118-185A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203366692 | |||||||
| chr2:203367088 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0308 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.285+44A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203367088 | |||||||
| chr2:203367128 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.285+84T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203367128 | |||||||
| chr2:203367323 | C | CT | 182 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(179): Show |
182 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.285+292dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203367323 | ||||||
| chr2:203367337 | A | T | 2 | a0001c0001t0001g0266 a0001c0001t0037g0320 |
2 | HG02109.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.285+293A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203367337 | |||||||
| chr2:203367551 | T | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+507T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203367551 | |||||||
| chr2:203367819 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.285+775A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203367819 | |||||||
| chr2:203367873 | G | A | 95 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(92): Show |
95 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.285+829G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203367873 | |||||||
| chr2:203367876 | C | T | 3 | a0001c0001t0011g0153 a0001c0001t0011g0154 a0001c0001t0011g0155 |
3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.285+832C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203367876 | |||||||
| chr2:203368222 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.285+1178C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368222 | |||||||
| chr2:203368228 | T | G | 2 | a0001c0001t0003g0191 a0001c0001t0003g0192 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.285+1184T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368228 | |||||||
| chr2:203368585 | T | G | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+1541T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368585 | |||||||
| chr2:203368818 | A | AT | 6 | a0001c0001t0001g0201 a0001c0001t0001g0245 a0001c0001t0002g0093 others(3): Show |
6 | HG01169.hp2 HG01358.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+1788dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203368818 | ||||||
| chr2:203368984 | AT | A | 16 | a0001c0001t0001g0181 a0001c0001t0001g0224 a0001c0001t0001g0234 others(13): Show |
16 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.285+1972delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203368984 | ||||||
| chr2:203368984 | ATT | A | 80 | a0001c0001t0001g0186 a0001c0001t0001g0202 a0001c0001t0001g0213 others(77): Show |
80 | HG00597.hp1 HG00609.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.285+1971_285+1972d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203368984 | ||||||
| chr2:203368984 | ATTT | A | 134 | a0001c0001t0001g0182 a0001c0001t0001g0200 a0001c0001t0001g0201 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.285+1970_285+1972d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203368984 | ||||||
| chr2:203368984 | ATTTT | A | 77 | a0001c0001t0001g0138 a0001c0001t0001g0270 a0001c0001t0002g0005 others(74): Show |
77 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.285+1969_285+1972d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203368984 | ||||||
| chr2:203368985 | T | A | 4 | a0001c0001t0001g0229 a0001c0001t0003g0208 a0001c0001t0006g0172 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+1941T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368985 | |||||||
| chr2:203368986 | T | A | 15 | a0001c0001t0001g0181 a0001c0001t0001g0224 a0001c0001t0001g0234 others(12): Show |
15 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(12): Show |
intron_variant | MODIFIER | c.285+1942T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368986 | |||||||
| chr2:203368987 | T | A | 77 | a0001c0001t0001g0186 a0001c0001t0001g0202 a0001c0001t0001g0213 others(74): Show |
77 | HG00597.hp1 HG00609.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.285+1943T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368987 | |||||||
| chr2:203368988 | T | A | 119 | a0001c0001t0001g0182 a0001c0001t0001g0200 a0001c0001t0001g0201 others(116): Show |
119 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.285+1944T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368988 | |||||||
| chr2:203368989 | T | A | 69 | a0001c0001t0001g0270 a0001c0001t0002g0005 a0001c0001t0002g0006 others(66): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.285+1945T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368989 | |||||||
| chr2:203368990 | T | A | 5 | a0001c0001t0002g0045 a0001c0001t0009g0158 a0001c0001t0009g0159 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+1946T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368990 | |||||||
| chr2:203369054 | C | T | 1 | a0001c0001t0005g0156 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.285+2010C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369054 | |||||||
| chr2:203369150 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.285+2106G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369150 | |||||||
| chr2:203369203 | A | G | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285+2159A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369203 | |||||||
| chr2:203369230 | T | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.285+2186T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369230 | |||||||
| chr2:203369357 | G | A | 1 | a0001c0001t0002g0007 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.285+2313G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369357 | |||||||
| chr2:203369385 | A | G | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.285+2341A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369385 | |||||||
| chr2:203369592 | G | A | 301 | a0001c0001t0001g0138 a0001c0001t0001g0181 a0001c0001t0001g0182 others(298): Show |
301 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.285+2548G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369592 | |||||||
| chr2:203369774 | G | T | 1 | a0001c0001t0004g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.285+2730G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369774 | |||||||
| chr2:203369937 | C | T | 2 | a0001c0002t0005g0116 a0001c0002t0024g0118 |
2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.285+2893C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369937 | |||||||
| chr2:203370122 | TTTG | T | 4 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+3080_285+3082d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370122 | ||||||
| chr2:203370165 | A | G | 7 | a0001c0001t0005g0106 a0001c0001t0005g0107 a0001c0001t0005g0108 others(4): Show |
7 | HG02083.hp1 HG02135.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+3121A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370165 | |||||||
| chr2:203370175 | T | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0277 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.285+3131T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370175 | |||||||
| chr2:203370176 | C | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0277 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.285+3132C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370176 | |||||||
| chr2:203370178 | T | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0277 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.285+3134T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370178 | |||||||
| chr2:203370180 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0277 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.285+3136C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370180 | |||||||
| chr2:203370186 | T | TTC | 23 | a0001c0001t0001g0138 a0001c0001t0001g0224 a0001c0001t0002g0018 others(20): Show |
23 | HG00741.hp1 HG01074.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.285+3182_285+3183d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | T | TTCTC | 4 | a0001c0001t0002g0030 a0001c0001t0004g0135 a0001c0001t0004g0144 others(1): Show |
4 | HG01943.hp2 HG02129.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+3180_285+3183d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | T | TTCTCTC | 7 | a0001c0001t0002g0023 a0001c0001t0002g0026 a0001c0001t0002g0027 others(4): Show |
7 | HG02083.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+3178_285+3183d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | T | TTCTCTCT others(1): Show |
7 | a0001c0001t0004g0141 a0001c0001t0004g0146 a0001c0001t0005g0081 others(4): Show |
7 | HG00621.hp1 HG02293.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+3176_285+3183d others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | T | TTCTCTCT others(3): Show |
7 | a0001c0001t0002g0024 a0001c0001t0005g0100 a0001c0001t0005g0106 others(4): Show |
7 | HG02040.hp2 HG02155.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+3174_285+3183d others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | T | TTCTCTCT others(5): Show |
3 | a0001c0001t0005g0104 a0001c0001t0005g0107 a0001c0001t0005g0115 |
3 | HG02293.hp2 HG03831.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.285+3172_285+3183d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | T | TTCTCTCT others(9): Show |
2 | a0001c0001t0005g0102 a0001c0001t0005g0161 |
2 | HG01257.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.285+3168_285+3183d others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | T | TTCTCTCT others(13): Show |
1 | a0001c0001t0005g0156 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.285+3164_285+3183d others(22): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | TTC | T | 6 | a0001c0001t0001g0244 a0001c0001t0001g0293 a0001c0001t0001g0318 others(3): Show |
6 | HG00673.hp1 HG01255.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.285+3182_285+3183d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | TTCTC | T | 94 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0200 others(91): Show |
94 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.285+3180_285+3183d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | TTCTCTC | T | 31 | a0001c0001t0001g0263 a0001c0001t0001g0307 a0001c0001t0002g0094 others(28): Show |
31 | HG00642.hp2 HG00738.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.285+3178_285+3183d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | TTCTCTCT others(1): Show |
T | 27 | a0001c0001t0001g0202 a0001c0001t0001g0218 a0001c0001t0001g0297 others(24): Show |
27 | HG00733.hp2 HG00735.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.285+3176_285+3183d others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | TTCTCTCT others(3): Show |
T | 17 | a0001c0001t0001g0186 a0001c0001t0001g0214 a0001c0001t0001g0215 others(14): Show |
17 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.285+3174_285+3183d others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | TTCTCTCT others(5): Show |
T | 3 | a0001c0001t0003g0203 a0001c0001t0010g0067 a0001c0001t0034g0190 |
3 | HG00438.hp1 NA18962.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.285+3172_285+3183d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | TTCTCTCT others(9): Show |
T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.285+3168_285+3183d others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370186 | TTCTCTCT others(11): Show |
T | 2 | a0001c0001t0007g0089 a0001c0001t0016g0088 |
2 | NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.285+3166_285+3183d others(20): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | ||||||
| chr2:203370227 | T | TC | 3 | a0001c0001t0002g0038 a0001c0001t0029g0096 a0001c0001t0032g0034 |
3 | HG02040.hp1 HG02080.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.285+3183_285+3184i others(3): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370227 | |||||||
| chr2:203370227 | T | TCTCTC | 3 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0004g0143 |
3 | HG02155.hp2 HG04228.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.285+3183_285+3184i others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370227 | |||||||
| chr2:203370227 | T | TCTCTCTC others(10): Show |
1 | a0001c0001t0005g0103 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.285+3183_285+3184i others(19): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370227 | |||||||
| chr2:203370320 | T | G | 2 | a0001c0001t0006g0149 a0001c0001t0006g0164 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.285+3276T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370320 | |||||||
| chr2:203370375 | AC | A | 10 | a0001c0001t0005g0106 a0001c0001t0005g0107 a0001c0001t0005g0108 others(7): Show |
10 | HG00621.hp1 HG02083.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+3333delC | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370375 | ||||||
| chr2:203370451 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.285+3407G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370451 | |||||||
| chr2:203370654 | A | G | 1 | a0001c0001t0018g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.285+3610A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370654 | |||||||
| chr2:203370753 | G | A | 186 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(183): Show |
186 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.285+3709G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370753 | |||||||
| chr2:203371049 | A | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.285+4005A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371049 | |||||||
| chr2:203371163 | G | A | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285+4119G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371163 | |||||||
| chr2:203371334 | C | A | 17 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.285+4290C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371334 | |||||||
| chr2:203371394 | A | G | 4 | a0001c0001t0003g0199 a0001c0001t0003g0221 a0001c0001t0003g0222 others(1): Show |
4 | HG00642.hp1 HG01358.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+4350A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371394 | |||||||
| chr2:203371537 | A | G | 3 | a0001c0001t0001g0259 a0001c0001t0001g0280 a0001c0001t0001g0292 |
3 | NA18978.hp1 NA18982.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.285+4493A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371537 | |||||||
| chr2:203371596 | C | A | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.285+4552C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371596 | |||||||
| chr2:203371824 | T | G | 1 | a0001c0001t0002g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.285+4780T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371824 | |||||||
| chr2:203371918 | A | C | 2 | a0001c0001t0002g0032 a0001c0001t0002g0039 |
2 | HG01074.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.285+4874A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371918 | |||||||
| chr2:203371941 | A | T | 288 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.285+4897A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371941 | |||||||
| chr2:203371958 | C | T | 2 | a0001c0001t0004g0139 a0001c0001t0004g0140 |
2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.285+4914C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371958 | |||||||
| chr2:203372019 | C | T | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+4975C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372019 | |||||||
| chr2:203372082 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.285+5038G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372082 | |||||||
| chr2:203372128 | C | T | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.285+5084C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372128 | |||||||
| chr2:203372244 | G | A | 1 | a0001c0001t0002g0058 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.285+5200G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372244 | |||||||
| chr2:203372245 | C | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | NA18949.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.285+5201C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372245 | |||||||
| chr2:203372261 | A | T | 91 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(88): Show |
91 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.285+5217A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372261 | |||||||
| chr2:203372291 | G | A | 3 | a0001c0001t0010g0066 a0001c0001t0010g0067 a0001c0001t0010g0078 |
3 | NA18962.hp2 NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.285+5247G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372291 | |||||||
| chr2:203372361 | C | T | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285+5317C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372361 | |||||||
| chr2:203372385 | C | G | 3 | a0001c0001t0001g0279 a0001c0001t0004g0145 a0001c0001t0004g0217 |
3 | HG02886.hp1 NA19057.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.285+5341C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372385 | |||||||
| chr2:203372417 | C | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0277 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.285+5373C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372417 | |||||||
| chr2:203372418 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0277 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.285+5374C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372418 | |||||||
| chr2:203372526 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.285+5482C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372526 | |||||||
| chr2:203372547 | C | T | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+5503C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372547 | |||||||
| chr2:203372552 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.285+5508G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372552 | |||||||
| chr2:203372725 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.285+5681C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372725 | |||||||
| chr2:203372728 | G | A | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.285+5684G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372728 | |||||||
| chr2:203372759 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.285+5715G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372759 | |||||||
| chr2:203372812 | C | T | 184 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(181): Show |
184 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.285+5768C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372812 | |||||||
| chr2:203372842 | T | C | 188 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(185): Show |
188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.285+5798T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372842 | |||||||
| chr2:203372865 | G | A | 3 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0144 |
3 | HG02559.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.285+5821G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372865 | |||||||
| chr2:203373198 | T | C | 290 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(287): Show |
290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.285+6154T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373198 | |||||||
| chr2:203373199 | G | A | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+6155G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373199 | |||||||
| chr2:203373245 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.285+6201G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373245 | |||||||
| chr2:203373246 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.285+6202C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373246 | |||||||
| chr2:203373247 | G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+6203G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373247 | |||||||
| chr2:203373328 | C | T | 1 | a0001c0001t0003g0185 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.285+6284C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373328 | |||||||
| chr2:203373336 | G | A | 1 | a0001c0001t0017g0260 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.285+6292G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373336 | |||||||
| chr2:203373356 | G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+6312G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373356 | |||||||
| chr2:203373496 | AGGGAGAG others(5): Show |
A | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+6464_285+6475d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203373496 | ||||||
| chr2:203373498 | G | A | 9 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0015 others(6): Show |
9 | HG00621.hp2 HG00741.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+6454G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373498 | |||||||
| chr2:203373533 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.285+6489T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373533 | |||||||
| chr2:203373603 | A | G | 1 | a0001c0001t0003g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.285+6559A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373603 | |||||||
| chr2:203373679 | C | A | 24 | a0001c0001t0003g0189 a0001c0001t0003g0191 a0001c0001t0003g0192 others(21): Show |
24 | HG00642.hp1 HG01074.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.286-6529C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373679 | |||||||
| chr2:203373710 | T | C | 3 | a0001c0001t0001g0138 a0001c0001t0004g0141 a0001c0001t0004g0145 |
3 | HG02293.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.286-6498T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373710 | |||||||
| chr2:203373714 | C | G | 3 | a0001c0001t0001g0138 a0001c0001t0004g0141 a0001c0001t0004g0145 |
3 | HG02293.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.286-6494C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373714 | |||||||
| chr2:203373748 | A | G | 1 | a0001c0001t0004g0128 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.286-6460A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373748 | |||||||
| chr2:203373766 | A | T | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.286-6442A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373766 | |||||||
| chr2:203373803 | A | AAGAGCTA others(19): Show |
1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.286-6404_286-6379d others(28): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203373803 | ||||||
| chr2:203373881 | G | A | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.286-6327G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373881 | |||||||
| chr2:203373973 | A | G | 1 | a0001c0001t0004g0128 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.286-6235A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373973 | |||||||
| chr2:203374065 | G | A | 184 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(181): Show |
184 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.286-6143G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203374065 | |||||||
| chr2:203374222 | G | C | 23 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0020 others(20): Show |
23 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.286-5986G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203374222 | |||||||
| chr2:203374227 | C | T | 1 | a0001c0001t0003g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.286-5981C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203374227 | |||||||
| chr2:203374316 | A | G | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.286-5892A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203374316 | |||||||
| chr2:203374405 | TAGG | T | 5 | a0001c0001t0002g0015 a0001c0001t0002g0025 a0001c0001t0002g0030 others(2): Show |
5 | HG00741.hp1 HG01256.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-5800_286-5798d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203374405 | ||||||
| chr2:203374498 | C | CA | 15 | a0001c0001t0001g0250 a0001c0001t0002g0080 a0001c0001t0002g0197 others(12): Show |
15 | HG00735.hp1 HG01975.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.286-5689dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203374498 | ||||||
| chr2:203374498 | C | CAA | 13 | a0001c0001t0004g0121 a0001c0001t0004g0123 a0001c0001t0004g0125 others(10): Show |
13 | HG00738.hp2 HG01943.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.286-5690_286-5689d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203374498 | ||||||
| chr2:203374530 | A | G | 1 | a0001c0001t0003g0193 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.286-5678A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203374530 | |||||||
| chr2:203374567 | G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.286-5641G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203374567 | |||||||
| chr2:203374943 | A | G | 2 | a0001c0001t0002g0037 a0001c0001t0002g0038 |
2 | HG02040.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.286-5265A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203374943 | |||||||
| chr2:203375000 | G | C | 6 | a0001c0001t0002g0024 a0001c0001t0002g0026 a0001c0001t0002g0027 others(3): Show |
6 | HG02486.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-5208G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203375000 | |||||||
| chr2:203375014 | C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.286-5194C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203375014 | |||||||
| chr2:203375280 | T | C | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.286-4928T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203375280 | |||||||
| chr2:203375661 | A | G | 1 | a0001c0001t0002g0008 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.286-4547A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203375661 | |||||||
| chr2:203375911 | C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.286-4297C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203375911 | |||||||
| chr2:203375927 | C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.286-4281C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203375927 | |||||||
| chr2:203375980 | A | G | 4 | a0001c0001t0004g0136 a0001c0001t0004g0137 a0001c0001t0004g0139 others(1): Show |
4 | HG02630.hp1 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-4228A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203375980 | |||||||
| chr2:203376168 | TC | T | 15 | a0001c0001t0003g0189 a0001c0001t0003g0199 a0001c0001t0003g0219 others(12): Show |
15 | HG00642.hp1 HG01074.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.286-4039delC | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203376168 | |||||||
| chr2:203376279 | T | A | 1 | a0001c0001t0001g0302 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.286-3929T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203376279 | |||||||
| chr2:203376561 | C | T | 7 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0045 others(4): Show |
7 | HG02523.hp2 NA18949.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.286-3647C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203376561 | |||||||
| chr2:203376733 | C | CT | 29 | a0001c0001t0001g0285 a0001c0001t0002g0040 a0001c0001t0002g0043 others(26): Show |
29 | HG00609.hp2 HG00621.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.286-3456dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203376733 | ||||||
| chr2:203376733 | C | CTT | 84 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0201 others(81): Show |
84 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.286-3457_286-3456d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203376733 | ||||||
| chr2:203376733 | C | CTTT | 10 | a0001c0001t0001g0200 a0001c0001t0001g0228 a0001c0001t0001g0232 others(7): Show |
10 | HG01175.hp1 HG02083.hp2 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.286-3458_286-3456d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203376733 | ||||||
| chr2:203376733 | CT | C | 9 | a0001c0001t0001g0181 a0001c0001t0001g0224 a0001c0001t0002g0026 others(6): Show |
9 | HG01884.hp2 HG02559.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.286-3456delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203376733 | ||||||
| chr2:203376829 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.286-3379G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203376829 | |||||||
| chr2:203376916 | A | G | 92 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.286-3292A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203376916 | |||||||
| chr2:203377365 | G | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0277 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.286-2843G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377365 | |||||||
| chr2:203377404 | TTTCATTT others(5): Show |
T | 4 | a0001c0001t0003g0206 a0001c0001t0003g0208 a0001c0001t0003g0209 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-2802_286-2791d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203377404 | ||||||
| chr2:203377608 | C | T | 7 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0045 others(4): Show |
7 | HG02523.hp2 NA18949.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.286-2600C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377608 | |||||||
| chr2:203377656 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.286-2552A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377656 | |||||||
| chr2:203377832 | A | G | 1 | a0001c0001t0002g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.286-2376A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377832 | |||||||
| chr2:203377891 | G | A | 6 | a0001c0001t0001g0229 a0001c0001t0001g0235 a0001c0001t0001g0236 others(3): Show |
6 | HG00438.hp2 HG00609.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-2317G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377891 | |||||||
| chr2:203377898 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.286-2310A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377898 | |||||||
| chr2:203377991 | T | C | 1 | a0001c0001t0003g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.286-2217T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377991 | |||||||
| chr2:203378114 | T | A | 1 | a0001c0001t0005g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.286-2094T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378114 | |||||||
| chr2:203378135 | T | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0277 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.286-2073T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378135 | |||||||
| chr2:203378151 | T | C | 1 | a0001c0001t0002g0007 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.286-2057T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378151 | |||||||
| chr2:203378174 | A | T | 39 | a0001c0001t0002g0187 a0001c0001t0002g0195 a0001c0001t0002g0197 others(36): Show |
39 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.286-2034A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378174 | |||||||
| chr2:203378177 | A | G | 95 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(92): Show |
95 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.286-2031A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378177 | |||||||
| chr2:203378207 | G | A | 26 | a0001c0001t0005g0098 a0001c0001t0005g0099 a0001c0001t0005g0100 others(23): Show |
26 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.286-2001G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378207 | |||||||
| chr2:203378236 | C | A | 5 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0057 others(2): Show |
5 | HG01081.hp1 NA18970.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-1972C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378236 | |||||||
| chr2:203378258 | A | G | 84 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(81): Show |
84 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.286-1950A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378258 | |||||||
| chr2:203378313 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.286-1895G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378313 | |||||||
| chr2:203378313 | G | T | 78 | a0001c0001t0001g0181 a0001c0001t0001g0224 a0001c0001t0001g0256 others(75): Show |
78 | HG00438.hp1 HG00621.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.286-1895G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378313 | |||||||
| chr2:203378322 | A | G | 2 | a0001c0001t0001g0271 a0001c0001t0002g0050 |
2 | HG02523.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.286-1886A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378322 | |||||||
| chr2:203378333 | G | C | 2 | a0001c0001t0001g0264 a0001c0001t0019g0147 |
2 | HG01081.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.286-1875G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378333 | |||||||
| chr2:203378358 | A | G | 1 | a0001c0001t0008g0036 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.286-1850A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378358 | |||||||
| chr2:203378362 | T | C | 1 | a0001c0001t0008g0036 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.286-1846T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378362 | |||||||
| chr2:203378386 | T | C | 22 | a0001c0001t0001g0234 a0001c0001t0002g0195 a0001c0001t0006g0001 others(19): Show |
22 | HG00423.hp1 HG00733.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.286-1822T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378386 | |||||||
| chr2:203378401 | A | G | 1 | a0001c0001t0036g0075 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.286-1807A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378401 | |||||||
| chr2:203378447 | A | G | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.286-1761A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378447 | |||||||
| chr2:203378865 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.286-1343C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378865 | |||||||
| chr2:203379036 | A | T | 42 | a0001c0001t0002g0187 a0001c0001t0002g0195 a0001c0001t0002g0197 others(39): Show |
42 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.286-1172A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379036 | |||||||
| chr2:203379128 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.286-1080G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379128 | |||||||
| chr2:203379184 | G | A | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.286-1024G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379184 | |||||||
| chr2:203379514 | C | T | 5 | a0001c0001t0007g0004 a0001c0001t0007g0084 a0001c0001t0007g0090 others(2): Show |
5 | NA18951.hp1 NA18968.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-694C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379514 | |||||||
| chr2:203379519 | C | CT | 5 | a0001c0001t0002g0082 a0001c0001t0002g0097 a0001c0001t0007g0089 others(2): Show |
5 | HG02165.hp2 NA18940.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-688dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203379519 | ||||||
| chr2:203379649 | G | A | 17 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.286-559G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379649 | |||||||
| chr2:203379706 | T | A | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.286-502T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379706 | |||||||
| chr2:203379724 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.286-484G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379724 | |||||||
| chr2:203379894 | A | G | 1 | a0001c0001t0004g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.286-314A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379894 | |||||||
| chr2:203379922 | T | G | 2 | a0001c0001t0010g0066 a0001c0001t0010g0067 |
2 | NA18962.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.286-286T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379922 | |||||||
| chr2:203379931 | T | G | 1 | a0001c0001t0005g0110 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.286-277T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379931 | |||||||
| chr2:203380777 | G | C | 188 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(185): Show |
188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.462+393G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203380777 | |||||||
| chr2:203380921 | C | G | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.462+537C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203380921 | |||||||
| chr2:203381163 | T | G | 1 | a0001c0001t0001g0262 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.462+779T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381163 | |||||||
| chr2:203381260 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.462+876A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381260 | |||||||
| chr2:203381303 | G | A | 1 | a0001c0001t0023g0111 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.463-886G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381303 | |||||||
| chr2:203381303 | G | T | 1 | a0001c0001t0005g0113 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.463-886G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381303 | |||||||
| chr2:203381384 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.463-805T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381384 | |||||||
| chr2:203381649 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.463-540T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381649 | |||||||
| chr2:203381821 | T | A | 28 | a0001c0001t0005g0081 a0001c0001t0005g0098 a0001c0001t0005g0099 others(25): Show |
28 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(25): Show |
intron_variant | MODIFIER | c.463-368T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381821 | |||||||
| chr2:203381999 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.463-190A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381999 | |||||||
| chr2:203382007 | C | T | 1 | a0001c0001t0018g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.463-182C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203382007 | |||||||
| chr2:203382417 | G | T | 24 | a0001c0001t0005g0100 a0001c0001t0005g0102 a0001c0001t0005g0103 others(21): Show |
24 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.480+211G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203382417 | |||||||
| chr2:203382652 | A | G | 1 | a0001c0001t0004g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.480+446A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203382652 | |||||||
| chr2:203382747 | C | T | 1 | a0001c0001t0006g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.480+541C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203382747 | |||||||
| chr2:203382868 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.480+662A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203382868 | |||||||
| chr2:203383522 | A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.480+1316A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203383522 | |||||||
| chr2:203383689 | C | G | 1 | a0001c0002t0024g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.480+1483C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203383689 | |||||||
| chr2:203383836 | T | C | 1 | a0001c0001t0001g0213 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.480+1630T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203383836 | |||||||
| chr2:203383842 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.480+1636C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203383842 | |||||||
| chr2:203383883 | C | A | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.480+1677C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203383883 | |||||||
| chr2:203383949 | C | G | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.480+1743C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203383949 | |||||||
| chr2:203384244 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.480+2038A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384244 | |||||||
| chr2:203384275 | C | CTTGTTTT others(5): Show |
21 | a0001c0001t0001g0138 a0001c0001t0002g0030 a0001c0001t0004g0121 others(18): Show |
21 | HG00738.hp2 HG01884.hp2 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.480+2078_480+2089d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384275 | ||||||
| chr2:203384275 | CTTGTTT | C | 38 | a0001c0001t0002g0187 a0001c0001t0003g0184 a0001c0001t0003g0185 others(35): Show |
38 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.480+2084_480+2089d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384275 | ||||||
| chr2:203384284 | GTTTTTGT others(10): Show |
G | 4 | a0001c0001t0001g0274 a0001c0001t0002g0195 a0001c0001t0002g0197 others(1): Show |
4 | HG00735.hp1 HG01496.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+2084_480+2100d others(19): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384284 | ||||||
| chr2:203384285 | TTTTTG | T | 121 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(118): Show |
121 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.480+2084_480+2088d others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384285 | ||||||
| chr2:203384286 | TTTTG | T | 18 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(15): Show |
18 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.480+2084_480+2087d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384286 | ||||||
| chr2:203384290 | G | GTTTTTGT others(6): Show |
7 | a0001c0001t0004g0123 a0001c0001t0004g0131 a0001c0001t0004g0136 others(4): Show |
7 | HG02132.hp2 HG02523.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.480+2089_480+2090i others(15): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384290 | ||||||
| chr2:203384290 | G | GTTTTTGT others(5): Show |
1 | a0001c0001t0004g0141 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.480+2089_480+2090i others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384290 | ||||||
| chr2:203384290 | G | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0059 |
3 | NA18954.hp2 NA18992.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.480+2084G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384290 | |||||||
| chr2:203384290 | GT | G | 47 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(44): Show |
47 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.480+2118delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384290 | ||||||
| chr2:203384291 | T | TTTTTGTT others(4): Show |
5 | a0001c0001t0004g0148 a0001c0001t0009g0158 a0001c0001t0009g0159 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+2089_480+2090i others(13): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384291 | ||||||
| chr2:203384299 | T | G | 11 | a0001c0001t0004g0123 a0001c0001t0004g0131 a0001c0001t0004g0136 others(8): Show |
11 | HG02109.hp2 HG02132.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.480+2093T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384299 | |||||||
| chr2:203384300 | T | G | 57 | a0001c0001t0001g0138 a0001c0001t0001g0292 a0001c0001t0002g0020 others(54): Show |
57 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.480+2094T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384300 | |||||||
| chr2:203384300 | T | TG | 4 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0003g0074 others(1): Show |
4 | NA18949.hp2 NA19003.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+2094_480+2095i others(3): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384300 | |||||||
| chr2:203384301 | T | G | 239 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(236): Show |
239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.480+2095T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384301 | |||||||
| chr2:203384305 | T | G | 2 | a0001c0001t0019g0147 a0001c0001t0022g0319 |
2 | HG01884.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.480+2099T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384305 | |||||||
| chr2:203384306 | T | G | 6 | a0001c0001t0002g0016 a0001c0001t0004g0148 a0001c0001t0009g0158 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.480+2100T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384306 | |||||||
| chr2:203384310 | T | G | 1 | a0001c0001t0004g0145 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.480+2104T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384310 | |||||||
| chr2:203384312 | T | G | 4 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+2106T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384312 | |||||||
| chr2:203384313 | T | G | 138 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(135): Show |
138 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.480+2107T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384313 | |||||||
| chr2:203384314 | T | G | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.480+2108T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384314 | |||||||
| chr2:203384317 | T | G | 186 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(183): Show |
186 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.480+2111T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384317 | |||||||
| chr2:203384451 | T | C | 1 | a0001c0001t0002g0014 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.480+2245T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384451 | |||||||
| chr2:203384676 | A | G | 92 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.480+2470A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384676 | |||||||
| chr2:203384810 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.480+2604G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384810 | |||||||
| chr2:203384820 | A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.480+2614A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384820 | |||||||
| chr2:203384888 | G | A | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.480+2682G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384888 | |||||||
| chr2:203385080 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.480+2874G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385080 | |||||||
| chr2:203385094 | A | G | 5 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+2888A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385094 | |||||||
| chr2:203385139 | C | CTTTTTT | 36 | a0001c0001t0002g0195 a0001c0001t0002g0197 a0001c0001t0002g0198 others(33): Show |
36 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.480+2941_480+2946d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | ||||||
| chr2:203385139 | C | CTTTTTTT others(1): Show |
20 | a0001c0001t0001g0275 a0001c0001t0006g0001 a0001c0001t0006g0149 others(17): Show |
20 | HG00323.hp2 HG00733.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.480+2939_480+2946d others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | ||||||
| chr2:203385139 | C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0264 others(1): Show |
4 | HG01081.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+2934_480+2946d others(15): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | ||||||
| chr2:203385139 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0005g0100 a0001c0002t0005g0116 |
2 | HG02976.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.480+2946_480+2947i others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | ||||||
| chr2:203385139 | C | CTTTTTTT others(10): Show |
16 | a0001c0001t0005g0081 a0001c0001t0005g0102 a0001c0001t0005g0103 others(13): Show |
16 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.480+2946_480+2947i others(19): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | ||||||
| chr2:203385139 | C | CTTTTTTT others(11): Show |
10 | a0001c0001t0005g0107 a0001c0001t0005g0113 a0001c0001t0005g0114 others(7): Show |
10 | HG02109.hp1 HG02451.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.480+2946_480+2947i others(20): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | ||||||
| chr2:203385139 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0227 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.480+2946_480+2947i others(21): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | ||||||
| chr2:203385139 | C | CTTTTTTT others(13): Show |
29 | a0001c0001t0001g0186 a0001c0001t0001g0202 a0001c0001t0001g0212 others(26): Show |
29 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.480+2946_480+2947i others(22): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | ||||||
| chr2:203385139 | C | CTTTTTTT others(14): Show |
33 | a0001c0001t0001g0182 a0001c0001t0001g0200 a0001c0001t0001g0201 others(30): Show |
33 | HG00438.hp2 HG01109.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.480+2946_480+2947i others(23): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | ||||||
| chr2:203385139 | C | CTTTTTTT others(15): Show |
17 | a0001c0001t0001g0181 a0001c0001t0001g0214 a0001c0001t0001g0218 others(14): Show |
17 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.480+2946_480+2947i others(24): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | ||||||
| chr2:203385139 | C | CTTTTTTT others(16): Show |
8 | a0001c0001t0001g0215 a0001c0001t0001g0228 a0001c0001t0001g0237 others(5): Show |
8 | HG00741.hp2 HG02083.hp2 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.480+2946_480+2947i others(25): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | ||||||
| chr2:203385139 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0018g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.480+2946_480+2947i others(27): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | ||||||
| chr2:203385139 | C | CTTTTTTT others(19): Show |
3 | a0001c0001t0001g0224 a0001c0001t0001g0244 a0001c0001t0001g0277 |
3 | HG03139.hp1 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.480+2946_480+2947i others(28): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | ||||||
| chr2:203385139 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0292 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.480+2946_480+2947i others(29): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | ||||||
| chr2:203385157 | C | CAG | 188 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(185): Show |
188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.480+2952_480+2953d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385157 | ||||||
| chr2:203385352 | C | T | 1 | a0001c0001t0005g0151 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.480+3146C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385352 | |||||||
| chr2:203385460 | A | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.480+3254A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385460 | |||||||
| chr2:203385693 | A | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.480+3487A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385693 | |||||||
| chr2:203385729 | C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.480+3523C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385729 | |||||||
| chr2:203385750 | G | T | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.480+3544G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385750 | |||||||
| chr2:203385919 | T | C | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.480+3713T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385919 | |||||||
| chr2:203385966 | T | G | 20 | a0001c0001t0005g0100 a0001c0001t0005g0102 a0001c0001t0005g0103 others(17): Show |
20 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.480+3760T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385966 | |||||||
| chr2:203386174 | A | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.480+3968A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386174 | |||||||
| chr2:203386261 | C | A | 1 | a0001c0001t0003g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.480+4055C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386261 | |||||||
| chr2:203386321 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.480+4115C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386321 | |||||||
| chr2:203386361 | G | C | 1 | a0001c0001t0004g0141 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.480+4155G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386361 | |||||||
| chr2:203386366 | C | T | 4 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0297 others(1): Show |
4 | HG00735.hp2 HG00741.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+4160C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386366 | |||||||
| chr2:203386393 | G | A | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.480+4187G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386393 | |||||||
| chr2:203386430 | G | GT | 64 | a0001c0001t0001g0182 a0001c0001t0001g0228 a0001c0001t0001g0231 others(61): Show |
64 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.480+4250dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203386430 | ||||||
| chr2:203386430 | G | GTT | 7 | a0001c0001t0001g0224 a0001c0001t0001g0292 a0001c0001t0003g0191 others(4): Show |
7 | HG02135.hp2 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.480+4249_480+4250d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203386430 | ||||||
| chr2:203386430 | G | GTTTTTTT others(2): Show |
7 | a0001c0001t0006g0150 a0001c0001t0006g0162 a0001c0001t0006g0163 others(4): Show |
7 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.480+4242_480+4250d others(11): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203386430 | ||||||
| chr2:203386430 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0006g0164 a0001c0001t0006g0173 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.480+4241_480+4250d others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203386430 | ||||||
| chr2:203386430 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0006g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.480+4239_480+4250d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203386430 | ||||||
| chr2:203386430 | GT | G | 94 | a0001c0001t0001g0138 a0001c0001t0001g0181 a0001c0001t0002g0006 others(91): Show |
94 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.480+4250delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203386430 | ||||||
| chr2:203386542 | T | G | 1 | a0001c0001t0008g0085 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.480+4336T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386542 | |||||||
| chr2:203386640 | C | CT | 52 | a0001c0001t0001g0271 a0001c0001t0001g0294 a0001c0001t0001g0306 others(49): Show |
52 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.481-4389dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203386640 | ||||||
| chr2:203386657 | T | C | 1 | a0001c0001t0005g0110 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.481-4389T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386657 | |||||||
| chr2:203386747 | C | T | 3 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0021g0152 |
3 | HG00621.hp1 NA18992.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.481-4299C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386747 | |||||||
| chr2:203386962 | C | T | 1 | a0001c0001t0018g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.481-4084C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386962 | |||||||
| chr2:203387056 | C | CT | 90 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(87): Show |
90 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.481-3970dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203387056 | ||||||
| chr2:203387056 | CT | C | 126 | a0001c0001t0001g0138 a0001c0001t0002g0002 a0001c0001t0002g0005 others(123): Show |
126 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.481-3970delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203387056 | ||||||
| chr2:203387074 | TTTC | T | 19 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(16): Show |
19 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.481-3971_481-3969d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203387074 | |||||||
| chr2:203387075 | TTC | T | 68 | a0001c0001t0002g0187 a0001c0001t0002g0195 a0001c0001t0002g0197 others(65): Show |
68 | HG00438.hp1 HG00621.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.481-3970_481-3969d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203387075 | |||||||
| chr2:203387076 | TC | T | 5 | a0001c0001t0003g0184 a0001c0001t0003g0185 a0001c0001t0022g0319 others(2): Show |
5 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-3966delC | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203387076 | ||||||
| chr2:203387077 | C | T | 94 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(91): Show |
94 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.481-3969C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203387077 | |||||||
| chr2:203387211 | A | G | 1 | a0001c0001t0006g0170 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.481-3835A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203387211 | |||||||
| chr2:203387602 | A | G | 10 | a0001c0001t0001g0138 a0001c0001t0004g0136 a0001c0001t0004g0137 others(7): Show |
10 | HG02293.hp1 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-3444A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203387602 | |||||||
| chr2:203387854 | G | C | 1 | a0001c0001t0001g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.481-3192G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203387854 | |||||||
| chr2:203387856 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.481-3190C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203387856 | |||||||
| chr2:203388185 | C | T | 16 | a0001c0001t0003g0189 a0001c0001t0003g0199 a0001c0001t0003g0219 others(13): Show |
16 | HG00642.hp1 HG01074.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.481-2861C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388185 | |||||||
| chr2:203388186 | G | A | 26 | a0001c0001t0005g0098 a0001c0001t0005g0099 a0001c0001t0005g0100 others(23): Show |
26 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.481-2860G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388186 | |||||||
| chr2:203388503 | C | T | 1 | a0001c0001t0013g0105 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.481-2543C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388503 | |||||||
| chr2:203388622 | A | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.481-2424A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388622 | |||||||
| chr2:203388667 | C | T | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.481-2379C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388667 | |||||||
| chr2:203388687 | T | A | 5 | a0001c0001t0003g0184 a0001c0001t0003g0185 a0001c0001t0019g0147 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-2359T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388687 | |||||||
| chr2:203388693 | T | A | 2 | a0001c0001t0004g0127 a0001c0001t0004g0132 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.481-2353T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388693 | |||||||
| chr2:203388885 | T | C | 9 | a0001c0001t0002g0024 a0001c0001t0002g0026 a0001c0001t0002g0027 others(6): Show |
9 | HG02145.hp1 HG02486.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.481-2161T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388885 | |||||||
| chr2:203388944 | A | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.481-2102A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388944 | |||||||
| chr2:203388955 | G | A | 5 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0001c0001t0003g0208 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-2091G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388955 | |||||||
| chr2:203389008 | T | C | 9 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(6): Show |
9 | HG02129.hp1 HG02132.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.481-2038T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203389008 | |||||||
| chr2:203389077 | T | C | 2 | a0001c0001t0006g0001 a0001c0001t0028g0167 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.481-1969T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203389077 | |||||||
| chr2:203389189 | T | C | 1 | a0001c0001t0006g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.481-1857T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203389189 | |||||||
| chr2:203389847 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.481-1199G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203389847 | |||||||
| chr2:203389850 | A | C | 1 | a0001c0001t0007g0004 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.481-1196A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203389850 | |||||||
| chr2:203389919 | G | C | 2 | a0001c0001t0003g0208 a0001c0001t0003g0209 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.481-1127G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203389919 | |||||||
| chr2:203390093 | A | C | 2 | a0001c0001t0010g0066 a0001c0001t0010g0067 |
2 | NA18962.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.481-953A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203390093 | |||||||
| chr2:203390257 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.481-789C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203390257 | |||||||
| chr2:203390443 | G | A | 1 | a0001c0002t0024g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.481-603G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203390443 | |||||||
| chr2:203390447 | C | T | 2 | a0001c0002t0005g0116 a0001c0002t0024g0118 |
2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.481-599C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203390447 | |||||||
| chr2:203390633 | G | GA | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.481-402dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203390633 | ||||||
| chr2:203390716 | A | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.481-330A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203390716 | |||||||
| chr2:203391301 | A | G | 1 | a0001c0001t0002g0040 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.578+158A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203391301 | |||||||
| chr2:203391714 | G | A | 25 | a0001c0001t0005g0081 a0001c0001t0005g0100 a0001c0001t0005g0102 others(22): Show |
25 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.578+571G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203391714 | |||||||
| chr2:203391820 | C | CA | 42 | a0001c0001t0001g0265 a0001c0001t0001g0268 a0001c0001t0001g0301 others(39): Show |
42 | HG00733.hp2 HG00738.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.578+695dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203391820 | ||||||
| chr2:203392258 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.578+1115C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392258 | |||||||
| chr2:203392263 | G | GCACCACC others(5): Show |
1 | a0001c0001t0001g0234 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.578+1131_578+1132i others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392263 | ||||||
| chr2:203392275 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.578+1132T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392275 | |||||||
| chr2:203392275 | T | TCAC | 62 | a0001c0001t0001g0181 a0001c0001t0002g0005 a0001c0001t0002g0010 others(59): Show |
62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.578+1171_578+1173d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | ||||||
| chr2:203392275 | T | TCACCAC | 52 | a0001c0001t0001g0224 a0001c0001t0001g0277 a0001c0001t0001g0294 others(49): Show |
52 | HG00438.hp1 HG00597.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.578+1168_578+1173d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | ||||||
| chr2:203392275 | T | TCACCACC others(2): Show |
46 | a0001c0001t0001g0182 a0001c0001t0001g0247 a0001c0001t0001g0258 others(43): Show |
46 | HG00621.hp1 HG00642.hp1 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.578+1165_578+1173d others(11): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | ||||||
| chr2:203392275 | T | TCACCACC others(5): Show |
28 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(25): Show |
28 | HG00323.hp2 HG00735.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.578+1162_578+1173d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | ||||||
| chr2:203392275 | T | TCACCACC others(8): Show |
48 | a0001c0001t0001g0186 a0001c0001t0001g0200 a0001c0001t0001g0201 others(45): Show |
48 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.578+1159_578+1173d others(17): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | ||||||
| chr2:203392275 | T | TCACCACC others(11): Show |
17 | a0001c0001t0001g0207 a0001c0001t0001g0229 a0001c0001t0001g0235 others(14): Show |
17 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.578+1156_578+1173d others(20): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | ||||||
| chr2:203392275 | T | TCACCACC others(14): Show |
4 | a0001c0001t0001g0268 a0001c0001t0001g0272 a0001c0001t0001g0274 others(1): Show |
4 | HG01515.hp1 HG03834.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.578+1153_578+1173d others(23): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | ||||||
| chr2:203392275 | T | TCACCACC others(17): Show |
1 | a0001c0001t0001g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.578+1150_578+1173d others(26): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | ||||||
| chr2:203392275 | TCAC | T | 8 | a0001c0001t0001g0138 a0001c0001t0002g0002 a0001c0001t0002g0009 others(5): Show |
8 | HG01168.hp1 HG02027.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.578+1171_578+1173d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | ||||||
| chr2:203392275 | TCACCAC | T | 9 | a0001c0001t0002g0021 a0001c0001t0002g0195 a0001c0001t0002g0197 others(6): Show |
9 | HG00735.hp1 HG01167.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.578+1168_578+1173d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | ||||||
| chr2:203392275 | TCACCACC others(2): Show |
T | 3 | a0001c0001t0004g0148 a0001c0001t0005g0098 a0001c0001t0005g0099 |
3 | HG02486.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.578+1165_578+1173d others(11): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | ||||||
| chr2:203392314 | C | CCAA | 6 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0015 others(3): Show |
6 | HG00609.hp2 HG01168.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.578+1199_578+1201d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | ||||||
| chr2:203392314 | C | CCAACAA | 3 | a0001c0001t0002g0008 a0001c0001t0002g0021 a0001c0001t0004g0148 |
3 | HG03098.hp2 HG03491.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.578+1196_578+1201d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | ||||||
| chr2:203392314 | CCAA | C | 40 | a0001c0001t0001g0138 a0001c0001t0002g0005 a0001c0001t0002g0011 others(37): Show |
40 | HG00323.hp1 HG01074.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.578+1199_578+1201d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | ||||||
| chr2:203392314 | CCAACAA | C | 20 | a0001c0001t0002g0007 a0001c0001t0002g0019 a0001c0001t0002g0051 others(17): Show |
20 | HG00621.hp1 HG01192.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.578+1196_578+1201d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | ||||||
| chr2:203392314 | CCAACAAC others(2): Show |
C | 39 | a0001c0001t0001g0181 a0001c0001t0002g0093 a0001c0001t0002g0195 others(36): Show |
39 | HG00438.hp1 HG00642.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.578+1193_578+1201d others(11): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | ||||||
| chr2:203392314 | CCAACAAC others(5): Show |
C | 27 | a0001c0001t0001g0218 a0001c0001t0001g0224 a0001c0001t0001g0236 others(24): Show |
27 | HG01433.hp2 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.578+1190_578+1201d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | ||||||
| chr2:203392314 | CCAACAAC others(8): Show |
C | 103 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(100): Show |
103 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.578+1187_578+1201d others(17): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | ||||||
| chr2:203392314 | CCAACAAC others(11): Show |
C | 21 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0245 others(18): Show |
21 | HG00673.hp1 HG01081.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.578+1184_578+1201d others(20): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | ||||||
| chr2:203392317 | A | C | 1 | a0001c0001t0001g0243 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.578+1174A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392317 | |||||||
| chr2:203392318 | C | T | 4 | a0001c0001t0004g0136 a0001c0001t0004g0137 a0001c0001t0004g0139 others(1): Show |
4 | HG02630.hp1 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.578+1175C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392318 | |||||||
| chr2:203392320 | A | C | 5 | a0001c0001t0001g0243 a0001c0001t0004g0136 a0001c0001t0004g0137 others(2): Show |
5 | HG02630.hp1 HG02723.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.578+1177A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392320 | |||||||
| chr2:203392323 | A | C | 1 | a0001c0001t0001g0243 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.578+1180A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392323 | |||||||
| chr2:203392326 | A | C | 1 | a0001c0001t0001g0243 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.578+1183A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392326 | |||||||
| chr2:203392329 | A | C | 1 | a0001c0001t0001g0243 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.578+1186A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392329 | |||||||
| chr2:203392332 | A | C | 1 | a0001c0001t0001g0243 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.578+1189A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392332 | |||||||
| chr2:203392335 | A | C | 1 | a0001c0001t0001g0243 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.578+1192A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392335 | |||||||
| chr2:203392500 | T | G | 21 | a0001c0001t0005g0081 a0001c0001t0005g0100 a0001c0001t0005g0102 others(18): Show |
21 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.578+1357T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392500 | |||||||
| chr2:203392529 | C | G | 1 | a0001c0001t0002g0007 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.578+1386C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392529 | |||||||
| chr2:203392900 | A | G | 1 | a0001c0001t0031g0183 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.578+1757A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392900 | |||||||
| chr2:203392950 | A | G | 1 | a0001c0001t0015g0119 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.579-1750A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392950 | |||||||
| chr2:203392967 | C | CT | 154 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(151): Show |
154 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.579-1723dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392967 | ||||||
| chr2:203392977 | T | A | 29 | a0001c0001t0001g0138 a0001c0001t0004g0121 a0001c0001t0004g0123 others(26): Show |
29 | HG00738.hp2 HG01943.hp1 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.579-1723T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392977 | |||||||
| chr2:203392978 | A | T | 2 | a0001c0001t0002g0018 a0001c0001t0027g0117 |
2 | HG02055.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.579-1722A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392978 | |||||||
| chr2:203393108 | T | G | 1 | a0001c0001t0002g0083 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.579-1592T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203393108 | |||||||
| chr2:203393110 | A | G | 3 | a0001c0001t0006g0162 a0001c0001t0006g0168 a0001c0001t0006g0169 |
3 | HG00733.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.579-1590A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203393110 | |||||||
| chr2:203393197 | G | A | 1 | a0001c0002t0024g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.579-1503G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203393197 | |||||||
| chr2:203393203 | C | T | 92 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.579-1497C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203393203 | |||||||
| chr2:203393422 | C | G | 1 | a0001c0001t0003g0194 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.579-1278C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203393422 | |||||||
| chr2:203393970 | T | C | 1 | a0001c0001t0018g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.579-730T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203393970 | |||||||
| chr2:203394018 | T | A | 10 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0250 others(7): Show |
10 | HG00323.hp2 HG01257.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.579-682T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203394018 | |||||||
| chr2:203394163 | G | A | 1 | a0001c0001t0002g0033 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.579-537G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203394163 | |||||||
| chr2:203394400 | G | GA | 222 | a0001c0001t0001g0138 a0001c0001t0001g0181 a0001c0001t0001g0182 others(219): Show |
222 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.579-300_579-299ins others(1): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203394400 | |||||||
| chr2:203395306 | C | T | 1 | a0001c0001t0003g0189 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.726-350C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395306 | |||||||
| chr2:203395432 | A | AAT | 20 | a0001c0001t0001g0224 a0001c0001t0004g0145 a0001c0001t0004g0146 others(17): Show |
20 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.726-208_726-207dup others(2): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395432 | ||||||
| chr2:203395432 | A | AATATAT | 4 | a0001c0001t0005g0099 a0001c0001t0009g0158 a0001c0001t0009g0159 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-212_726-207dup others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395432 | ||||||
| chr2:203395432 | A | AATATATA others(1): Show |
5 | a0001c0001t0001g0201 a0001c0001t0001g0245 a0001c0001t0001g0246 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.726-214_726-207dup others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395432 | ||||||
| chr2:203395432 | A | AATATATA others(3): Show |
5 | a0001c0001t0001g0251 a0001c0001t0001g0285 a0001c0001t0001g0295 others(2): Show |
5 | HG00597.hp1 HG03688.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.726-216_726-207dup others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395432 | ||||||
| chr2:203395432 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.726-220_726-207dup others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395432 | ||||||
| chr2:203395432 | A | AATATATA others(15): Show |
1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.726-207_726-206ins others(22): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395432 | ||||||
| chr2:203395446 | T | TAC | 5 | a0001c0001t0002g0009 a0001c0001t0002g0037 a0001c0001t0002g0062 others(2): Show |
5 | HG01168.hp1 HG01175.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.726-209_726-208ins others(2): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395446 | ||||||
| chr2:203395446 | T | TACAC | 3 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0053 |
3 | HG00323.hp1 HG03490.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.726-209_726-208ins others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395446 | ||||||
| chr2:203395448 | T | C | 12 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(9): Show |
12 | HG00323.hp1 HG01168.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.726-208T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395448 | |||||||
| chr2:203395448 | T | TAC | 63 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(60): Show |
63 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.726-172_726-171dup others(2): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TACAC | 9 | a0001c0001t0001g0258 a0001c0001t0002g0016 a0001c0001t0002g0017 others(6): Show |
9 | HG00621.hp1 HG00621.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.726-174_726-171dup others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TACACACA others(3): Show |
2 | a0001c0001t0003g0206 a0001c0001t0003g0210 |
2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.726-180_726-171dup others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TACACACA others(5): Show |
2 | a0001c0001t0003g0191 a0001c0001t0003g0192 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.726-182_726-171dup others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATACACA others(5): Show |
4 | a0001c0001t0003g0205 a0001c0001t0003g0208 a0001c0001t0003g0209 others(1): Show |
4 | HG01192.hp1 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATACACA others(7): Show |
3 | a0001c0001t0003g0225 a0001c0001t0003g0317 a0001c0001t0027g0117 |
3 | HG01255.hp2 HG02055.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.726-207_726-206ins others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATACACA others(9): Show |
1 | a0001c0001t0003g0288 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.726-207_726-206ins others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATACA others(3): Show |
2 | a0001c0001t0001g0299 a0001c0001t0003g0289 |
2 | HG01515.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.726-207_726-206ins others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATACA others(5): Show |
9 | a0001c0001t0002g0195 a0001c0001t0002g0197 a0001c0001t0002g0198 others(6): Show |
9 | HG00438.hp1 HG00735.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATACA others(7): Show |
10 | a0001c0001t0003g0189 a0001c0001t0003g0199 a0001c0001t0003g0219 others(7): Show |
10 | HG00642.hp1 HG01074.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATACA others(9): Show |
5 | a0001c0001t0002g0187 a0001c0001t0003g0188 a0001c0001t0003g0223 others(2): Show |
5 | HG00642.hp2 HG01433.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATACA others(13): Show |
1 | a0001c0001t0034g0190 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.726-207_726-206ins others(20): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATATA others(3): Show |
3 | a0001c0001t0001g0243 a0001c0001t0001g0304 a0001c0001t0001g0316 |
3 | NA18945.hp1 NA18980.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.726-207_726-206ins others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATATA others(5): Show |
3 | a0001c0001t0001g0275 a0001c0001t0001g0302 a0001c0001t0003g0196 |
3 | HG00323.hp2 HG00738.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.726-207_726-206ins others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATATA others(7): Show |
3 | a0001c0001t0003g0184 a0001c0001t0003g0185 a0001c0001t0031g0183 |
3 | HG01891.hp1 HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.726-207_726-206ins others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATATA others(3): Show |
10 | a0001c0001t0001g0216 a0001c0001t0001g0234 a0001c0001t0001g0241 others(7): Show |
10 | HG00423.hp1 HG00733.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATATA others(5): Show |
8 | a0001c0001t0001g0207 a0001c0001t0001g0259 a0001c0001t0001g0265 others(5): Show |
8 | HG01255.hp1 HG01981.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0186 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.726-207_726-206ins others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATATA others(9): Show |
1 | a0001c0001t0001g0274 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.726-207_726-206ins others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATATA others(5): Show |
33 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0218 others(30): Show |
33 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATATA others(7): Show |
10 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0228 others(7): Show |
10 | HG01496.hp2 HG02083.hp2 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATATA others(9): Show |
1 | a0001c0001t0001g0293 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.726-207_726-206ins others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATATA others(7): Show |
5 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0239 others(2): Show |
5 | HG00438.hp2 HG00735.hp2 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATATA others(9): Show |
1 | a0001c0001t0001g0308 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.726-207_726-206ins others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | T | TATATATA others(11): Show |
1 | a0001c0001t0001g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.726-207_726-206ins others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395448 | TAC | T | 25 | a0001c0001t0002g0041 a0001c0001t0002g0055 a0001c0001t0002g0069 others(22): Show |
25 | HG00738.hp2 HG00741.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.726-172_726-171del others(2): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | ||||||
| chr2:203395450 | C | T | 55 | a0001c0001t0001g0138 a0001c0001t0001g0280 a0001c0001t0004g0133 others(52): Show |
55 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.726-206C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395450 | |||||||
| chr2:203395452 | C | T | 56 | a0001c0001t0001g0138 a0001c0001t0001g0280 a0001c0001t0004g0121 others(53): Show |
56 | HG00738.hp2 HG01257.hp1 HG01258.hp1 others(53): Show |
intron_variant | MODIFIER | c.726-204C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395452 | |||||||
| chr2:203395454 | C | T | 5 | a0001c0001t0006g0001 a0001c0001t0011g0153 a0001c0001t0011g0154 others(2): Show |
5 | HG02109.hp1 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.726-202C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395454 | |||||||
| chr2:203395456 | C | T | 4 | a0001c0001t0011g0153 a0001c0001t0011g0154 a0001c0001t0011g0155 others(1): Show |
4 | HG02109.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-200C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395456 | |||||||
| chr2:203395458 | C | T | 4 | a0001c0001t0011g0153 a0001c0001t0011g0154 a0001c0001t0011g0155 others(1): Show |
4 | HG02109.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-198C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395458 | |||||||
| chr2:203395460 | C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.726-196C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395460 | |||||||
| chr2:203395462 | C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.726-194C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395462 | |||||||
| chr2:203395486 | T | A | 1 | a0001c0001t0002g0076 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.726-170T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395486 | |||||||
| chr2:203395543 | C | T | 2 | a0001c0001t0002g0187 a0001c0001t0003g0188 |
2 | NA18952.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.726-113C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395543 | |||||||
| chr2:203395885 | T | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0277 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.850+105T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 7/11 | chr2 | 203395885 | |||||||
| chr2:203396118 | G | A | 1 | a0001c0001t0005g0151 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.850+338G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 7/11 | chr2 | 203396118 | |||||||
| chr2:203396367 | T | A | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.851-418T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 7/11 | chr2 | 203396367 | |||||||
| chr2:203396463 | A | C | 1 | a0001c0002t0005g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.851-322A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 7/11 | chr2 | 203396463 | |||||||
| chr2:203396712 | T | C | 29 | a0001c0001t0005g0081 a0001c0001t0005g0098 a0001c0001t0005g0099 others(26): Show |
29 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.851-73T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 7/11 | chr2 | 203396712 | |||||||
| chr2:203397000 | G | C | 188 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(185): Show |
188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1033+33G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397000 | |||||||
| chr2:203397067 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1033+100G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397067 | |||||||
| chr2:203397218 | A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1033+251A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397218 | |||||||
| chr2:203397220 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1033+253A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397220 | |||||||
| chr2:203397264 | G | C | 1 | a0001c0001t0001g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1033+297G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397264 | |||||||
| chr2:203397540 | C | T | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1033+573C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397540 | |||||||
| chr2:203397773 | C | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0049 |
2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1033+806C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397773 | |||||||
| chr2:203397903 | G | C | 73 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0207 others(70): Show |
73 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1033+936G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397903 | |||||||
| chr2:203398313 | A | G | 4 | a0001c0001t0002g0195 a0001c0001t0002g0197 a0001c0001t0002g0198 others(1): Show |
4 | HG00735.hp1 HG01496.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1033+1346A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398313 | |||||||
| chr2:203398482 | T | C | 1 | a0001c0001t0003g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1033+1515T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398482 | |||||||
| chr2:203398507 | G | A | 1 | a0001c0001t0012g0130 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1033+1540G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398507 | |||||||
| chr2:203398632 | G | A | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1033+1665G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398632 | |||||||
| chr2:203398645 | C | T | 1 | a0001c0001t0023g0111 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1033+1678C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398645 | |||||||
| chr2:203398693 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1033+1726C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398693 | |||||||
| chr2:203398757 | T | C | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1033+1790T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398757 | |||||||
| chr2:203398799 | A | G | 1 | a0001c0001t0002g0011 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1033+1832A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398799 | |||||||
| chr2:203398854 | A | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1033+1887A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398854 | |||||||
| chr2:203398906 | G | A | 1 | a0001c0001t0005g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1033+1939G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398906 | |||||||
| chr2:203399533 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1033+2566C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203399533 | |||||||
| chr2:203399598 | C | G | 1 | a0001c0001t0004g0127 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1033+2631C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203399598 | |||||||
| chr2:203399738 | CTCCTGAC others(10): Show |
C | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1033+2772_1033+278 others(21): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203399738 | |||||||
| chr2:203399890 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1034-2686T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203399890 | |||||||
| chr2:203399999 | C | T | 1 | a0001c0001t0018g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1034-2577C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203399999 | |||||||
| chr2:203400079 | C | CT | 23 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0020 others(20): Show |
23 | HG00423.hp2 HG00621.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1034-2469dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 203400079 | ||||||
| chr2:203400079 | CT | C | 38 | a0001c0001t0001g0271 a0001c0001t0001g0290 a0001c0001t0001g0291 others(35): Show |
38 | HG00738.hp2 HG01192.hp2 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.1034-2469delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 203400079 | ||||||
| chr2:203400079 | CTT | C | 17 | a0001c0001t0001g0207 a0001c0001t0001g0232 a0001c0001t0001g0244 others(14): Show |
17 | HG00735.hp2 HG00741.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1034-2470_1034-246 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 203400079 | ||||||
| chr2:203400079 | CTTT | C | 110 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(107): Show |
110 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1034-2471_1034-246 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 203400079 | ||||||
| chr2:203400079 | CTTTT | C | 59 | a0001c0001t0001g0181 a0001c0001t0001g0214 a0001c0001t0001g0230 others(56): Show |
59 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1034-2472_1034-246 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 203400079 | ||||||
| chr2:203400115 | A | T | 1 | a0001c0001t0001g0229 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1034-2461A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203400115 | |||||||
| chr2:203400173 | C | T | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1034-2403C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203400173 | |||||||
| chr2:203400679 | G | C | 1 | a0001c0001t0001g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1034-1897G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203400679 | |||||||
| chr2:203401150 | G | A | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1034-1426G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203401150 | |||||||
| chr2:203401207 | C | T | 188 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(185): Show |
188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1034-1369C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203401207 | |||||||
| chr2:203401335 | C | T | 1 | a0001c0001t0003g0225 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1034-1241C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203401335 | |||||||
| chr2:203401362 | C | T | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1034-1214C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203401362 | |||||||
| chr2:203401620 | T | C | 73 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0207 others(70): Show |
73 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1034-956T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203401620 | |||||||
| chr2:203401770 | G | A | 3 | a0001c0001t0008g0036 a0001c0001t0008g0042 a0001c0001t0032g0034 |
3 | NA18999.hp1 NA19057.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1034-806G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203401770 | |||||||
| chr2:203402159 | C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1034-417C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203402159 | |||||||
| chr2:203402171 | A | G | 15 | a0001c0001t0003g0189 a0001c0001t0003g0199 a0001c0001t0003g0219 others(12): Show |
15 | HG00642.hp1 HG01074.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1034-405A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203402171 | |||||||
| chr2:203402179 | C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1034-397C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203402179 | |||||||
| chr2:203402310 | C | T | 3 | a0001c0001t0001g0181 a0001c0001t0001g0224 a0001c0001t0001g0277 |
3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1034-266C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203402310 | |||||||
| chr2:203402330 | C | T | 5 | a0001c0001t0010g0066 a0001c0001t0010g0067 a0001c0001t0010g0068 others(2): Show |
5 | HG02080.hp1 NA18962.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.1034-246C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203402330 | |||||||
| chr2:203402349 | A | G | 1 | a0001c0001t0008g0085 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1034-227A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203402349 | |||||||
| chr2:203402367 | A | G | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1034-209A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203402367 | |||||||
| chr2:203402769 | G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1192+35G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203402769 | |||||||
| chr2:203402831 | G | T | 29 | a0001c0001t0001g0138 a0001c0001t0004g0121 a0001c0001t0004g0123 others(26): Show |
29 | HG00738.hp2 HG01943.hp1 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.1192+97G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203402831 | |||||||
| chr2:203403179 | C | T | 2 | a0001c0001t0006g0172 a0001c0001t0006g0178 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1192+445C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403179 | |||||||
| chr2:203403244 | A | G | 1 | a0001c0001t0003g0074 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1192+510A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403244 | |||||||
| chr2:203403359 | A | G | 1 | a0001c0001t0003g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1192+625A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403359 | |||||||
| chr2:203403475 | T | C | 4 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192+741T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403475 | |||||||
| chr2:203403510 | A | G | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1192+776A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403510 | |||||||
| chr2:203403645 | T | TTA | 189 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(186): Show |
189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1192+915_1192+916d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203403645 | ||||||
| chr2:203403733 | T | G | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1192+999T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403733 | |||||||
| chr2:203403742 | G | GT | 24 | a0001c0001t0001g0227 a0001c0001t0001g0230 a0001c0001t0001g0246 others(21): Show |
24 | HG00673.hp2 HG01074.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1192+1030dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203403742 | ||||||
| chr2:203403742 | G | GTT | 121 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(118): Show |
121 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1192+1029_1192+103 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203403742 | ||||||
| chr2:203403742 | G | GTTT | 50 | a0001c0001t0001g0231 a0001c0001t0001g0272 a0001c0001t0001g0291 others(47): Show |
50 | HG00597.hp1 HG00621.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1192+1028_1192+103 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203403742 | ||||||
| chr2:203403742 | GT | G | 11 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0015 others(8): Show |
11 | HG00323.hp1 HG00741.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.1192+1030delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203403742 | ||||||
| chr2:203403782 | C | T | 92 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1192+1048C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403782 | |||||||
| chr2:203403903 | G | A | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1192+1169G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403903 | |||||||
| chr2:203404031 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1192+1297G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404031 | |||||||
| chr2:203404032 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1192+1298C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404032 | |||||||
| chr2:203404033 | G | A | 1 | a0001c0001t0005g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1192+1299G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404033 | |||||||
| chr2:203404102 | T | G | 1 | a0001c0001t0001g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1192+1368T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404102 | |||||||
| chr2:203404109 | T | C | 2 | a0001c0001t0003g0191 a0001c0001t0003g0192 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1192+1375T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404109 | |||||||
| chr2:203404273 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1192+1539A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404273 | |||||||
| chr2:203404369 | G | A | 4 | a0001c0001t0010g0066 a0001c0001t0010g0067 a0001c0001t0010g0068 others(1): Show |
4 | NA18962.hp2 NA18986.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192+1635G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404369 | |||||||
| chr2:203404442 | A | G | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG00735.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1192+1708A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404442 | |||||||
| chr2:203404546 | C | T | 21 | a0001c0001t0005g0098 a0001c0001t0006g0001 a0001c0001t0006g0149 others(18): Show |
21 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.1192+1812C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404546 | |||||||
| chr2:203404547 | G | C | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG00735.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1192+1813G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404547 | |||||||
| chr2:203404700 | A | G | 3 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0003g0079 |
3 | HG00323.hp1 HG01168.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1192+1966A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404700 | |||||||
| chr2:203404763 | C | T | 189 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(186): Show |
189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1192+2029C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404763 | |||||||
| chr2:203404764 | G | A | 10 | a0001c0001t0001g0138 a0001c0001t0004g0136 a0001c0001t0004g0137 others(7): Show |
10 | HG02293.hp1 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1192+2030G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404764 | |||||||
| chr2:203404773 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1192+2039G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404773 | |||||||
| chr2:203404774 | G | C | 1 | a0001c0001t0001g0227 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1192+2040G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404774 | |||||||
| chr2:203404886 | G | A | 2 | a0001c0001t0004g0127 a0001c0001t0004g0132 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1192+2152G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404886 | |||||||
| chr2:203405045 | C | T | 27 | a0001c0001t0005g0081 a0001c0001t0005g0098 a0001c0001t0005g0099 others(24): Show |
27 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.1192+2311C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203405045 | |||||||
| chr2:203405197 | C | A | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1192+2463C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203405197 | |||||||
| chr2:203405460 | C | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1192+2726C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203405460 | |||||||
| chr2:203405597 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1192+2863G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203405597 | |||||||
| chr2:203405769 | A | G | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1192+3035A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203405769 | |||||||
| chr2:203405801 | T | C | 1 | a0001c0001t0005g0100 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1192+3067T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203405801 | |||||||
| chr2:203406119 | G | A | 2 | a0001c0001t0003g0191 a0001c0001t0003g0192 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1192+3385G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406119 | |||||||
| chr2:203406141 | A | C | 3 | a0001c0001t0001g0259 a0001c0001t0001g0280 a0001c0001t0001g0292 |
3 | NA18978.hp1 NA18982.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1192+3407A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406141 | |||||||
| chr2:203406231 | G | A | 189 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(186): Show |
189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1192+3497G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406231 | |||||||
| chr2:203406379 | G | C | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1192+3645G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406379 | |||||||
| chr2:203406409 | A | G | 1 | a0001c0001t0001g0293 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1192+3675A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406409 | |||||||
| chr2:203406448 | A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1192+3714A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406448 | |||||||
| chr2:203406494 | G | C | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1192+3760G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406494 | |||||||
| chr2:203406573 | G | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0308 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1192+3839G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406573 | |||||||
| chr2:203406688 | A | G | 1 | a0001c0001t0038g0048 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1192+3954A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406688 | |||||||
| chr2:203406767 | G | A | 1 | a0001c0001t0009g0177 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1192+4033G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406767 | |||||||
| chr2:203406788 | C | T | 42 | a0001c0001t0002g0187 a0001c0001t0002g0195 a0001c0001t0002g0197 others(39): Show |
42 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1192+4054C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406788 | |||||||
| chr2:203406820 | C | T | 6 | a0001c0001t0007g0004 a0001c0001t0007g0084 a0001c0001t0007g0089 others(3): Show |
6 | NA18951.hp1 NA18968.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192+4086C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406820 | |||||||
| chr2:203406903 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1192+4169T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406903 | |||||||
| chr2:203407338 | G | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1193-3947G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407338 | |||||||
| chr2:203407367 | C | T | 92 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1193-3918C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407367 | |||||||
| chr2:203407630 | C | G | 1 | a0001c0001t0003g0199 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1193-3655C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407630 | |||||||
| chr2:203407717 | A | G | 17 | a0001c0001t0004g0121 a0001c0001t0004g0123 a0001c0001t0004g0124 others(14): Show |
17 | HG00738.hp2 HG01943.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.1193-3568A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407717 | |||||||
| chr2:203407732 | A | G | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1193-3553A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407732 | |||||||
| chr2:203407733 | T | C | 8 | a0001c0001t0004g0123 a0001c0001t0004g0125 a0001c0001t0004g0128 others(5): Show |
8 | HG02129.hp1 HG02132.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1193-3552T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407733 | |||||||
| chr2:203407857 | A | G | 5 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(2): Show |
5 | HG00323.hp1 HG01168.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193-3428A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407857 | |||||||
| chr2:203407963 | T | G | 2 | a0001c0001t0004g0127 a0001c0001t0004g0132 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1193-3322T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407963 | |||||||
| chr2:203408021 | T | C | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1193-3264T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408021 | |||||||
| chr2:203408095 | A | C | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1193-3190A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408095 | |||||||
| chr2:203408109 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1193-3176C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408109 | |||||||
| chr2:203408165 | CT | C | 190 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(187): Show |
190 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1193-3106delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408165 | ||||||
| chr2:203408251 | C | T | 3 | a0001c0001t0001g0181 a0001c0001t0001g0224 a0001c0001t0001g0277 |
3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1193-3034C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408251 | |||||||
| chr2:203408265 | C | T | 7 | a0001c0001t0002g0018 a0001c0001t0002g0033 a0001c0001t0002g0045 others(4): Show |
7 | HG02523.hp2 NA18949.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.1193-3020C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408265 | |||||||
| chr2:203408288 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1193-2997G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408288 | |||||||
| chr2:203408343 | A | G | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1193-2942A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408343 | |||||||
| chr2:203408635 | T | C | 4 | a0001c0001t0001g0201 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1193-2650T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408635 | |||||||
| chr2:203408788 | C | G | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1193-2497C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408788 | |||||||
| chr2:203408828 | C | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1193-2457C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408828 | |||||||
| chr2:203408829 | C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1193-2456C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408829 | |||||||
| chr2:203408833 | C | CTTTCTTT others(4): Show |
2 | a0001c0001t0005g0113 a0001c0001t0005g0114 |
2 | NA18992.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1193-2449_1193-244 others(15): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | ||||||
| chr2:203408833 | C | CTTTCTTT others(5): Show |
16 | a0001c0001t0005g0081 a0001c0001t0005g0102 a0001c0001t0005g0103 others(13): Show |
16 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1193-2449_1193-244 others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | ||||||
| chr2:203408833 | C | CTTTCTTT others(6): Show |
6 | a0001c0001t0005g0100 a0001c0001t0005g0115 a0001c0001t0005g0156 others(3): Show |
6 | HG02109.hp1 HG02809.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1193-2449_1193-244 others(17): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | ||||||
| chr2:203408833 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0214 a0001c0001t0001g0233 a0001c0001t0006g0168 |
3 | HG01169.hp1 HG03491.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1193-2445_1193-243 others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | ||||||
| chr2:203408833 | C | CTTTTTTT others(4): Show |
106 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(103): Show |
106 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1193-2446_1193-243 others(15): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | ||||||
| chr2:203408833 | C | CTTTTTTT others(5): Show |
45 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0224 others(42): Show |
45 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1193-2447_1193-243 others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | ||||||
| chr2:203408833 | C | CTTTTTTT others(6): Show |
4 | a0001c0001t0003g0208 a0001c0001t0027g0117 a0001c0002t0005g0116 others(1): Show |
4 | HG02055.hp2 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1193-2448_1193-243 others(17): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | ||||||
| chr2:203408833 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0031g0183 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1193-2449_1193-243 others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | ||||||
| chr2:203408833 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1193-2450_1193-243 others(19): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | ||||||
| chr2:203408878 | T | C | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1193-2407T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408878 | |||||||
| chr2:203408900 | G | A | 1 | a0001c0001t0036g0075 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1193-2385G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408900 | |||||||
| chr2:203408924 | C | T | 28 | a0001c0001t0001g0138 a0001c0001t0004g0121 a0001c0001t0004g0123 others(25): Show |
28 | HG00738.hp2 HG01943.hp1 HG01975.hp1 others(25): Show |
intron_variant | MODIFIER | c.1193-2361C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408924 | |||||||
| chr2:203408995 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1193-2290C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408995 | |||||||
| chr2:203408996 | G | C | 1 | a0001c0001t0001g0316 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1193-2289G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408996 | |||||||
| chr2:203409086 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1193-2199C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409086 | |||||||
| chr2:203409133 | C | T | 1 | a0001c0001t0002g0040 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1193-2152C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409133 | |||||||
| chr2:203409226 | A | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1193-2059A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409226 | |||||||
| chr2:203409589 | C | T | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1193-1696C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409589 | |||||||
| chr2:203409595 | C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1193-1690C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409595 | |||||||
| chr2:203409674 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1193-1611T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409674 | |||||||
| chr2:203409857 | T | C | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1193-1428T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409857 | |||||||
| chr2:203409973 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1193-1312G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409973 | |||||||
| chr2:203410194 | A | T | 1 | a0001c0001t0015g0120 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1193-1091A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203410194 | |||||||
| chr2:203410306 | T | C | 22 | a0001c0001t0005g0081 a0001c0001t0005g0100 a0001c0001t0005g0102 others(19): Show |
22 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1193-979T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203410306 | |||||||
| chr2:203410338 | T | C | 1 | a0001c0001t0016g0088 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1193-947T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203410338 | |||||||
| chr2:203410963 | A | G | 1 | a0001c0001t0003g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1193-322A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203410963 | |||||||
| chr2:203410999 | TTA | T | 29 | a0001c0001t0001g0138 a0001c0001t0004g0121 a0001c0001t0004g0123 others(26): Show |
29 | HG00738.hp2 HG01943.hp1 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.1193-284_1193-283d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203410999 | ||||||
| chr2:203411604 | T | C | 92 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1279+233T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203411604 | |||||||
| chr2:203411973 | G | T | 1 | a0001c0001t0001g0266 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1279+602G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203411973 | |||||||
| chr2:203412370 | T | C | 2 | a0001c0001t0003g0219 a0001c0001t0003g0288 |
2 | HG01978.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1279+999T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412370 | |||||||
| chr2:203412516 | T | C | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1279+1145T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412516 | |||||||
| chr2:203412567 | C | A | 1 | a0001c0001t0025g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1279+1196C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412567 | |||||||
| chr2:203412579 | T | C | 1 | a0001c0001t0003g0225 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1279+1208T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412579 | |||||||
| chr2:203412617 | GT | G | 137 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(134): Show |
137 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1279+1248delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203412617 | ||||||
| chr2:203412755 | A | G | 188 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(185): Show |
188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1279+1384A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412755 | |||||||
| chr2:203412766 | C | T | 3 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0021g0152 |
3 | HG00621.hp1 NA18992.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1279+1395C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412766 | |||||||
| chr2:203412885 | G | C | 189 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(186): Show |
189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1279+1514G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412885 | |||||||
| chr2:203412926 | C | T | 22 | a0001c0001t0005g0081 a0001c0001t0005g0100 a0001c0001t0005g0102 others(19): Show |
22 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1279+1555C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412926 | |||||||
| chr2:203413068 | G | A | 27 | a0001c0001t0005g0081 a0001c0001t0005g0098 a0001c0001t0005g0099 others(24): Show |
27 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.1279+1697G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413068 | |||||||
| chr2:203413119 | T | A | 1 | a0001c0001t0004g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1279+1748T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413119 | |||||||
| chr2:203413466 | T | G | 1 | a0001c0001t0001g0275 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1279+2095T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413466 | |||||||
| chr2:203413473 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1279+2102A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413473 | |||||||
| chr2:203413518 | C | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1279+2147C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413518 | |||||||
| chr2:203413527 | A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1279+2156A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413527 | |||||||
| chr2:203413596 | C | T | 189 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(186): Show |
189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1279+2225C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413596 | |||||||
| chr2:203413651 | G | A | 4 | a0001c0001t0002g0082 a0001c0001t0002g0097 a0001c0001t0016g0086 others(1): Show |
4 | HG02165.hp2 NA18940.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+2280G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413651 | |||||||
| chr2:203413897 | C | CCAG | 92 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1279+2527_1279+252 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203413897 | ||||||
| chr2:203413985 | T | A | 92 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1279+2614T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413985 | |||||||
| chr2:203414005 | T | C | 1 | a0001c0001t0018g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1279+2634T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203414005 | |||||||
| chr2:203414101 | C | CT | 10 | a0001c0001t0002g0019 a0001c0001t0002g0071 a0001c0001t0002g0080 others(7): Show |
10 | HG00621.hp2 HG01192.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.1279+2749dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203414101 | ||||||
| chr2:203414101 | CT | C | 28 | a0001c0001t0001g0181 a0001c0001t0001g0224 a0001c0001t0001g0277 others(25): Show |
28 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.1279+2749delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203414101 | ||||||
| chr2:203414101 | CTT | C | 92 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1279+2748_1279+274 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203414101 | ||||||
| chr2:203414345 | T | C | 16 | a0001c0001t0001g0200 a0001c0001t0001g0228 a0001c0001t0001g0229 others(13): Show |
16 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.1280-2563T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203414345 | |||||||
| chr2:203414393 | C | T | 1 | a0001c0001t0018g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1280-2515C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203414393 | |||||||
| chr2:203414442 | C | A | 189 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(186): Show |
189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1280-2466C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203414442 | |||||||
| chr2:203414455 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1280-2453C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203414455 | |||||||
| chr2:203414460 | C | G | 1 | a0001c0001t0002g0030 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1280-2448C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203414460 | |||||||
| chr2:203414850 | A | G | 1 | a0001c0001t0001g0276 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1280-2058A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203414850 | |||||||
| chr2:203415148 | A | G | 3 | a0001c0001t0002g0021 a0001c0001t0002g0023 a0001c0001t0002g0049 |
3 | HG03491.hp2 HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1280-1760A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415148 | |||||||
| chr2:203415191 | T | G | 29 | a0001c0001t0005g0081 a0001c0001t0005g0098 a0001c0001t0005g0099 others(26): Show |
29 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.1280-1717T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415191 | |||||||
| chr2:203415339 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1280-1569C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415339 | |||||||
| chr2:203415345 | C | T | 3 | a0001c0001t0003g0073 a0001c0001t0003g0219 a0001c0001t0003g0288 |
3 | HG01978.hp1 HG02148.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1280-1563C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415345 | |||||||
| chr2:203415366 | C | G | 1 | a0001c0001t0003g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1280-1542C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415366 | |||||||
| chr2:203415486 | G | A | 2 | a0001c0001t0004g0127 a0001c0001t0004g0132 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1280-1422G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415486 | |||||||
| chr2:203415542 | G | A | 3 | a0001c0001t0001g0181 a0001c0001t0001g0224 a0001c0001t0001g0277 |
3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1280-1366G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415542 | |||||||
| chr2:203415611 | C | T | 2 | a0001c0001t0002g0038 a0001c0001t0022g0319 |
2 | HG01884.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.1280-1297C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415611 | |||||||
| chr2:203415616 | C | CA | 63 | a0001c0001t0001g0182 a0001c0001t0001g0212 a0001c0001t0001g0227 others(60): Show |
63 | HG00423.hp2 HG00609.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1280-1265dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203415616 | ||||||
| chr2:203415616 | C | CAA | 8 | a0001c0001t0002g0002 a0001c0001t0003g0189 a0001c0001t0003g0222 others(5): Show |
8 | HG01074.hp1 HG01358.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1280-1266_1280-126 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203415616 | ||||||
| chr2:203415616 | C | CAAA | 12 | a0001c0001t0005g0081 a0001c0001t0005g0100 a0001c0001t0005g0102 others(9): Show |
12 | HG01257.hp1 HG01258.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1280-1267_1280-126 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203415616 | ||||||
| chr2:203415616 | C | CAAAA | 14 | a0001c0001t0005g0098 a0001c0001t0005g0106 a0001c0001t0005g0107 others(11): Show |
14 | HG00621.hp1 HG02040.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1280-1268_1280-126 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203415616 | ||||||
| chr2:203415616 | CA | C | 14 | a0001c0001t0001g0224 a0001c0001t0001g0235 a0001c0001t0001g0269 others(11): Show |
14 | HG00609.hp1 HG01496.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.1280-1265delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203415616 | ||||||
| chr2:203415616 | CAAAAAAA others(2): Show |
C | 24 | a0001c0001t0001g0138 a0001c0001t0004g0121 a0001c0001t0004g0123 others(21): Show |
24 | HG00738.hp2 HG01943.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.1280-1273_1280-126 others(13): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203415616 | ||||||
| chr2:203415689 | A | C | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1280-1219A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415689 | |||||||
| chr2:203415817 | G | A | 2 | a0001c0001t0003g0191 a0001c0001t0003g0192 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1280-1091G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415817 | |||||||
| chr2:203415879 | A | G | 187 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(184): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1280-1029A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415879 | |||||||
| chr2:203415929 | T | A | 137 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(134): Show |
137 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1280-979T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415929 | |||||||
| chr2:203416040 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1280-868C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416040 | |||||||
| chr2:203416186 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1280-722A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416186 | |||||||
| chr2:203416219 | C | T | 189 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(186): Show |
189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1280-689C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416219 | |||||||
| chr2:203416239 | C | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0318 |
2 | HG01255.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1280-669C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416239 | |||||||
| chr2:203416357 | G | A | 1 | a0001c0001t0025g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1280-551G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416357 | |||||||
| chr2:203416397 | G | A | 42 | a0001c0001t0002g0187 a0001c0001t0002g0195 a0001c0001t0002g0197 others(39): Show |
42 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1280-511G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416397 | |||||||
| chr2:203416440 | C | T | 2 | a0001c0001t0007g0089 a0001c0001t0007g0091 |
2 | NA18968.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1280-468C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416440 | |||||||
| chr2:203416538 | C | T | 2 | a0001c0001t0002g0031 a0001c0001t0002g0093 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1280-370C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416538 | |||||||
| chr2:203416724 | G | A | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1280-184G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416724 | |||||||
| chr2:203416746 | G | A | 1 | a0001c0001t0003g0203 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1280-162G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416746 | |||||||
| chr2:203416788 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1280-120G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416788 | |||||||
| chr2:203416835 | C | T | 1 | a0001c0001t0004g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1280-73C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416835 | |||||||
| chr2:203417272 | T | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1453+191T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203417272 | |||||||
| chr2:203417307 | G | A | 3 | a0001c0001t0011g0153 a0001c0001t0011g0154 a0001c0001t0011g0155 |
3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1453+226G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203417307 | |||||||
| chr2:203417393 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1453+312A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203417393 | |||||||
| chr2:203417564 | G | A | 3 | a0001c0001t0005g0110 a0001c0001t0005g0112 a0001c0001t0005g0151 |
3 | HG02083.hp1 HG02135.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1453+483G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203417564 | |||||||
| chr2:203417815 | C | T | 1 | a0001c0002t0024g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1453+734C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203417815 | |||||||
| chr2:203417944 | C | T | 1 | a0001c0001t0006g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1453+863C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203417944 | |||||||
| chr2:203418193 | A | C | 4 | a0001c0001t0005g0106 a0001c0001t0005g0107 a0001c0001t0005g0108 others(1): Show |
4 | HG02155.hp1 NA18747.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1453+1112A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203418193 | |||||||
| chr2:203418596 | A | G | 1 | a0001c0001t0018g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1453+1515A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203418596 | |||||||
| chr2:203418651 | T | G | 1 | a0001c0001t0025g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1453+1570T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203418651 | |||||||
| chr2:203418951 | A | T | 2 | a0001c0001t0002g0026 a0001c0001t0002g0029 |
2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1453+1870A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203418951 | |||||||
| chr2:203419106 | C | CT | 49 | a0001c0001t0001g0200 a0001c0001t0001g0297 a0001c0001t0002g0031 others(46): Show |
49 | HG00621.hp1 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1453+2045dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203419106 | ||||||
| chr2:203419106 | CT | C | 15 | a0001c0001t0001g0275 a0001c0001t0001g0280 a0001c0001t0001g0284 others(12): Show |
15 | HG00323.hp2 HG01256.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.1453+2045delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203419106 | ||||||
| chr2:203419171 | G | A | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1453+2090G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419171 | |||||||
| chr2:203419230 | C | T | 8 | a0001c0001t0001g0200 a0001c0001t0001g0228 a0001c0001t0001g0230 others(5): Show |
8 | HG02083.hp2 NA18939.hp2 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.1453+2149C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419230 | |||||||
| chr2:203419358 | A | G | 6 | a0001c0001t0007g0004 a0001c0001t0007g0084 a0001c0001t0007g0089 others(3): Show |
6 | NA18951.hp1 NA18968.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1453+2277A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419358 | |||||||
| chr2:203419461 | C | T | 1 | a0001c0001t0002g0058 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1453+2380C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419461 | |||||||
| chr2:203419568 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1453+2487G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419568 | |||||||
| chr2:203419672 | C | T | 1 | a0001c0001t0002g0047 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1453+2591C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419672 | |||||||
| chr2:203419801 | C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1453+2720C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419801 | |||||||
| chr2:203419870 | C | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1453+2789C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419870 | |||||||
| chr2:203419913 | C | A | 22 | a0001c0001t0005g0081 a0001c0001t0005g0100 a0001c0001t0005g0102 others(19): Show |
22 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1453+2832C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419913 | |||||||
| chr2:203419968 | A | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1453+2887A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419968 | |||||||
| chr2:203419973 | A | G | 2 | a0001c0001t0008g0022 a0001c0001t0008g0035 |
2 | HG00673.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1453+2892A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419973 | |||||||
| chr2:203420107 | T | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0308 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1453+3026T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420107 | |||||||
| chr2:203420217 | A | G | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1453+3136A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420217 | |||||||
| chr2:203420304 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1453+3223C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420304 | |||||||
| chr2:203420316 | T | TA | 3 | a0001c0001t0002g0020 a0001c0001t0002g0043 a0001c0001t0002g0058 |
3 | HG00423.hp2 HG00609.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1453+3236dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203420316 | ||||||
| chr2:203420396 | CT | C | 8 | a0001c0001t0001g0266 a0001c0001t0001g0276 a0001c0001t0002g0021 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.1453+3330delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203420396 | ||||||
| chr2:203420396 | CTT | C | 185 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(182): Show |
185 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1453+3329_1453+333 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203420396 | ||||||
| chr2:203420600 | A | G | 1 | a0001c0001t0002g0083 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1453+3519A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420600 | |||||||
| chr2:203420684 | C | T | 1 | a0001c0001t0003g0208 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1453+3603C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420684 | |||||||
| chr2:203420718 | C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1453+3637C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420718 | |||||||
| chr2:203420719 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1453+3638G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420719 | |||||||
| chr2:203420810 | T | G | 1 | a0001c0001t0003g0196 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1453+3729T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420810 | |||||||
| chr2:203420926 | G | A | 3 | a0001c0001t0002g0057 a0001c0001t0002g0070 a0001c0001t0002g0076 |
3 | NA18970.hp1 NA18991.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1453+3845G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420926 | |||||||
| chr2:203421051 | G | A | 39 | a0001c0001t0002g0187 a0001c0001t0002g0195 a0001c0001t0002g0197 others(36): Show |
39 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1453+3970G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203421051 | |||||||
| chr2:203421096 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1453+4015T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203421096 | |||||||
| chr2:203421603 | T | G | 3 | a0001c0001t0011g0153 a0001c0001t0011g0154 a0001c0001t0011g0155 |
3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1453+4522T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203421603 | |||||||
| chr2:203421929 | G | A | 2 | a0001c0002t0005g0116 a0001c0002t0024g0118 |
2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1453+4848G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203421929 | |||||||
| chr2:203421964 | C | CA | 39 | a0001c0001t0001g0138 a0001c0001t0001g0251 a0001c0001t0002g0024 others(36): Show |
39 | HG00673.hp2 HG00738.hp2 HG01433.hp1 others(36): Show |
intron_variant | MODIFIER | c.1453+4903dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203421964 | ||||||
| chr2:203421964 | C | CAAAA | 13 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(10): Show |
13 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1453+4900_1453+490 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203421964 | ||||||
| chr2:203421964 | C | CAAAAA | 6 | a0001c0001t0006g0171 a0001c0001t0006g0172 a0001c0001t0006g0173 others(3): Show |
6 | HG01109.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1453+4899_1453+490 others(9): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203421964 | ||||||
| chr2:203421964 | CA | C | 85 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0200 others(82): Show |
85 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1453+4903delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203421964 | ||||||
| chr2:203422126 | G | A | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1453+5045G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422126 | |||||||
| chr2:203422165 | G | T | 1 | a0001c0001t0004g0136 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1454-5012G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422165 | |||||||
| chr2:203422268 | G | GC | 221 | a0001c0001t0001g0138 a0001c0001t0001g0181 a0001c0001t0001g0182 others(218): Show |
221 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.1454-4909_1454-490 others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422268 | |||||||
| chr2:203422285 | C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1454-4892C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422285 | |||||||
| chr2:203422410 | G | A | 64 | a0001c0001t0001g0138 a0001c0001t0001g0224 a0001c0001t0001g0251 others(61): Show |
64 | HG00280.hp2 HG00621.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1454-4767G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422410 | |||||||
| chr2:203422411 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1454-4766C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422411 | |||||||
| chr2:203422492 | C | T | 1 | a0001c0001t0004g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1454-4685C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422492 | |||||||
| chr2:203422554 | A | G | 2 | a0001c0001t0001g0258 a0001c0001t0001g0282 |
2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1454-4623A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422554 | |||||||
| chr2:203422828 | T | C | 1 | a0001c0001t0006g0178 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1454-4349T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422828 | |||||||
| chr2:203423476 | A | C | 2 | a0001c0001t0005g0107 a0001c0001t0005g0108 |
2 | NA18965.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1454-3701A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423476 | |||||||
| chr2:203423477 | G | T | 2 | a0001c0001t0005g0107 a0001c0001t0005g0108 |
2 | NA18965.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1454-3700G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423477 | |||||||
| chr2:203423512 | G | A | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1454-3665G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423512 | |||||||
| chr2:203423530 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0308 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1454-3647A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423530 | |||||||
| chr2:203423710 | C | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0244 a0001c0001t0001g0308 |
3 | HG02622.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1454-3467C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423710 | |||||||
| chr2:203423711 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0277 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1454-3466G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423711 | |||||||
| chr2:203423714 | C | A | 6 | a0001c0001t0007g0004 a0001c0001t0007g0084 a0001c0001t0007g0089 others(3): Show |
6 | NA18951.hp1 NA18968.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1454-3463C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423714 | |||||||
| chr2:203423753 | A | G | 6 | a0001c0001t0006g0001 a0001c0001t0006g0162 a0001c0001t0006g0168 others(3): Show |
6 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1454-3424A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423753 | |||||||
| chr2:203423825 | T | A | 317 | a0001c0001t0001g0138 a0001c0001t0001g0181 a0001c0001t0001g0182 others(314): Show |
317 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.1454-3352T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423825 | |||||||
| chr2:203423979 | C | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1454-3198C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423979 | |||||||
| chr2:203423999 | C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1454-3178C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423999 | |||||||
| chr2:203424079 | T | G | 4 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0160 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1454-3098T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203424079 | |||||||
| chr2:203424091 | A | G | 17 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(14): Show |
17 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1454-3086A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203424091 | |||||||
| chr2:203424635 | G | C | 1 | a0001c0001t0001g0138 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1454-2542G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203424635 | |||||||
| chr2:203425008 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1454-2169C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425008 | |||||||
| chr2:203425012 | A | G | 1 | a0001c0001t0004g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1454-2165A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425012 | |||||||
| chr2:203425026 | A | AT | 13 | a0001c0001t0001g0216 a0001c0001t0001g0224 a0001c0001t0001g0254 others(10): Show |
13 | HG00621.hp1 HG00733.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1454-2134dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203425026 | ||||||
| chr2:203425026 | A | ATT | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1454-2135_1454-213 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203425026 | ||||||
| chr2:203425044 | G | T | 4 | a0001c0001t0004g0136 a0001c0001t0004g0137 a0001c0001t0004g0139 others(1): Show |
4 | HG02630.hp1 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-2133G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425044 | |||||||
| chr2:203425314 | T | C | 12 | a0001c0001t0002g0187 a0001c0001t0003g0188 a0001c0001t0003g0193 others(9): Show |
12 | HG00438.hp1 HG00642.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1454-1863T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425314 | |||||||
| chr2:203425322 | C | A | 1 | a0001c0001t0002g0055 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1454-1855C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425322 | |||||||
| chr2:203425798 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1454-1379G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425798 | |||||||
| chr2:203425806 | G | C | 15 | a0001c0001t0003g0189 a0001c0001t0003g0199 a0001c0001t0003g0219 others(12): Show |
15 | HG00642.hp1 HG01074.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1454-1371G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425806 | |||||||
| chr2:203425935 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1454-1242C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425935 | |||||||
| chr2:203426019 | C | CA | 51 | a0001c0001t0001g0138 a0001c0001t0001g0236 a0001c0001t0001g0300 others(48): Show |
51 | HG00733.hp2 HG00738.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1454-1140dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203426019 | ||||||
| chr2:203426040 | C | A | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1454-1137C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426040 | |||||||
| chr2:203426329 | T | C | 7 | a0001c0001t0008g0003 a0001c0001t0008g0022 a0001c0001t0008g0035 others(4): Show |
7 | HG00673.hp2 NA18946.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1454-848T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426329 | |||||||
| chr2:203426516 | T | C | 2 | a0001c0001t0005g0098 a0001c0001t0005g0099 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1454-661T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426516 | |||||||
| chr2:203426618 | A | T | 1 | a0001c0001t0002g0041 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1454-559A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426618 | |||||||
| chr2:203426677 | A | T | 1 | a0001c0001t0009g0160 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1454-500A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426677 | |||||||
| chr2:203426785 | TA | T | 255 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 others(252): Show |
255 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.1454-373delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203426785 | ||||||
| chr2:203426785 | TAA | T | 41 | a0001c0001t0001g0138 a0001c0001t0001g0224 a0001c0001t0001g0233 others(38): Show |
41 | HG00673.hp1 HG00738.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.1454-374_1454-373d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203426785 | ||||||
| chr2:203426798 | A | C | 1 | a0001c0001t0001g0234 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1454-379A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426798 | |||||||
| chr2:203426804 | AC | A | 3 | a0001c0001t0003g0203 a0001c0001t0003g0317 a0001c0001t0034g0190 |
3 | HG00438.hp1 HG03688.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1454-371delC | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203426804 | ||||||
| chr2:203426883 | A | G | 20 | a0001c0001t0006g0001 a0001c0001t0006g0149 a0001c0001t0006g0150 others(17): Show |
20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1454-294A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426883 | |||||||
| chr2:203426890 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1454-287A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426890 | |||||||
| chr2:203427147 | C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1454-30C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203427147 |