Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 85465 |
| ensemblid | ENSG00000138018.19 |
| hgncid | 29361 |
| symbol | SELENOI |
| name | selenoprotein I |
| refseq_nuc | NM_033505.4 |
| refseq_prot | NP_277040.1 |
| ensembl_nuc | ENST00000260585.12 |
| ensembl_prot | ENSP00000260585.7 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 26346143 |
| end | 26395885 |
| strand | + |
| ver | v1.2 |
| region | chr2:26346143-26395885 |
| region5000 | chr2:26341143-26400885 |
| regionname0 | SELENOI_chr2_26346143_26395885 |
| regionname5000 | SELENOI_chr2_26341143_26400885 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1191 | 211 | 62 | 53 | 77 | 7 | 12 | SELENOI_chr2_26341143_26400885 | SELENOI | ATGGC others(1186): Show |
chr2 | 26341143 | 26400885 | ||
| a0001c0002 | 0/1 | 1191 | 77 | 8 | 19 | 36 | 5 | 8 | SELENOI_chr2_26341143_26400885 | SELENOI | ATGGC others(1186): Show |
chr2 | 26341143 | 26400885 | ||
| a0001c0003 | 1/0 | 1191 | 32 | 11 | 4 | 16 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | ATGGC others(1186): Show |
chr2 | 26341143 | 26400885 | ||
| a0001c0004 | 0/0 | 1191 | 6 | 1 | 0 | 5 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | ATGGC others(1186): Show |
chr2 | 26341143 | 26400885 | ||
| a0001c0005 | 0/0 | 1191 | 6 | 6 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | ATGGC others(1186): Show |
chr2 | 26341143 | 26400885 | ||
| a0001c0006 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | ATGGC others(1186): Show |
chr2 | 26341143 | 26400885 | ||
| a0001c0007 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | ATGGC others(1186): Show |
chr2 | 26341143 | 26400885 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 8065 | 70 | 2 | 17 | 51 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0003 | 0/0 | 8065 | 54 | 16 | 22 | 2 | 7 | 7 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0005 | 0/0 | 8065 | 23 | 19 | 3 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0006 | 0/0 | 8065 | 10 | 10 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0007 | 0/0 | 8065 | 14 | 0 | 0 | 13 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0008 | 0/0 | 8061 | 9 | 7 | 2 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8056): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0009 | 0/0 | 8065 | 6 | 0 | 0 | 6 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0010 | 0/0 | 8065 | 6 | 3 | 3 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0013 | 0/0 | 8059 | 4 | 2 | 2 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8054): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0015 | 0/0 | 8059 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8054): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0016 | 0/0 | 8065 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0017 | 0/0 | 8065 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0018 | 0/0 | 8065 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0021 | 0/0 | 8065 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0022 | 0/0 | 8065 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0023 | 0/0 | 8065 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0024 | 0/0 | 8065 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0025 | 0/0 | 8065 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0027 | 0/0 | 8065 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0028 | 0/0 | 8065 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0029 | 0/0 | 8065 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0033 | 0/0 | 8065 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0034 | 0/0 | 8065 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0001t0035 | 0/0 | 8065 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0002t0001 | 0/1 | 8065 | 73 | 7 | 19 | 33 | 5 | 8 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0002t0005 | 0/0 | 8065 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0002t0030 | 0/0 | 8065 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0002t0031 | 0/0 | 8065 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0002t0032 | 0/0 | 8065 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0003t0004 | 0/0 | 8064 | 21 | 4 | 3 | 14 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8059): Show |
chr2 | 26341143 | 26400885 |
| a0001c0003t0011 | 0/0 | 8066 | 5 | 4 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8061): Show |
chr2 | 26341143 | 26400885 |
| a0001c0003t0012 | 1/0 | 8066 | 4 | 3 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8061): Show |
chr2 | 26341143 | 26400885 |
| a0001c0003t0019 | 0/0 | 8064 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8059): Show |
chr2 | 26341143 | 26400885 |
| a0001c0003t0020 | 0/0 | 8064 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8059): Show |
chr2 | 26341143 | 26400885 |
| a0001c0004t0004 | 0/0 | 8064 | 5 | 1 | 0 | 4 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8059): Show |
chr2 | 26341143 | 26400885 |
| a0001c0004t0014 | 0/0 | 8064 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8059): Show |
chr2 | 26341143 | 26400885 |
| a0001c0005t0006 | 0/0 | 8065 | 6 | 6 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0006t0006 | 0/0 | 8065 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| a0001c0007t0026 | 0/0 | 8065 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | GCCAT others(8060): Show |
chr2 | 26341143 | 26400885 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0006g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0007g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0007g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0007g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0008g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0008g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0008g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0008g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0009g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0009g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0009g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0009g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0009g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0010g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0010g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0010g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0010g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0010g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0013g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0013g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0013g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0013g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0015g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0016g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0017g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0018g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0021g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0022g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0023g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0024g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0025g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0027g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0028g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0029g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0033g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0034g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0001t0035g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0001 | 0/0 | 10 | 1 | 3 | 5 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0002 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0030g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0031g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0002t0032g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0011g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0012g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0012g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0012g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0012g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0019g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0003t0020g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0004t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0004t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0004t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0004t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0004t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0004t0014g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0005t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0005t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0005t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0005t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0005t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0005t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0006t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| a0001c0007t0026g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0070 | EUR | GBR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0016 | EUR | GBR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0014 | EUR | FIN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0073 | EUR | FIN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00408 | hp1 | a0001 | c0001 | t0007 | g0183 | EAS | CHS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | CHS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | CHS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | CHS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | CHS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | CHS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00558 | hp2 | a0001 | c0004 | t0004 | g0119 | EAS | CHS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00609 | hp1 | a0001 | c0001 | t0007 | g0047 | EAS | CHS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00642 | hp1 | a0001 | c0001 | t0029 | g0282 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | CHS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00733 | hp1 | a0001 | c0001 | t0013 | g0272 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0158 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00738 | hp2 | a0001 | c0003 | t0011 | g0010 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0238 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01069 | hp1 | a0001 | c0001 | t0010 | g0023 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01071 | hp2 | a0001 | c0001 | t0010 | g0023 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0108 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0022 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01106 | hp2 | a0001 | c0001 | t0010 | g0279 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01109 | hp2 | a0001 | c0001 | t0028 | g0283 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01167 | hp1 | a0001 | c0001 | t0013 | g0274 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01168 | hp1 | a0001 | c0003 | t0004 | g0169 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01169 | hp1 | a0001 | c0003 | t0004 | g0170 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01243 | hp1 | a0001 | c0003 | t0004 | g0153 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0072 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0268 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0285 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01433 | hp1 | a0001 | c0001 | t0027 | g0286 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0029 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0074 | EUR | IBS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0012 | EUR | IBS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0100 | EUR | IBS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | IBS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0258 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0255 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01928 | hp2 | a0001 | c0001 | t0035 | g0022 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0145 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0251 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0241 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02056 | hp2 | a0001 | c0003 | t0004 | g0234 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02071 | hp2 | a0001 | c0001 | t0033 | g0046 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02080 | hp1 | a0001 | c0001 | t0007 | g0050 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02135 | hp2 | a0001 | c0001 | t0007 | g0048 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02145 | hp2 | a0001 | c0003 | t0011 | g0010 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02155 | hp2 | a0001 | c0001 | t0025 | g0019 | EAS | CDX | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CDX | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0284 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02258 | hp2 | a0001 | c0003 | t0004 | g0161 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0253 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | KHV | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0028 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02602 | hp1 | a0001 | c0001 | t0016 | g0079 | SAS | PJL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0280 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0287 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02622 | hp2 | a0001 | c0001 | t0021 | g0264 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0242 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0275 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0259 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0256 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0104 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0266 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02818 | hp1 | a0001 | c0003 | t0012 | g0036 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02886 | hp1 | a0001 | c0003 | t0011 | g0039 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02886 | hp2 | a0001 | c0006 | t0006 | g0027 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0278 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0263 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0035 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02922 | hp2 | a0001 | c0001 | t0010 | g0281 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02965 | hp1 | a0001 | c0003 | t0011 | g0010 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0270 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0265 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0269 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0252 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02976 | hp2 | a0001 | c0002 | t0005 | g0159 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03041 | hp1 | a0001 | c0005 | t0006 | g0166 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03041 | hp2 | a0001 | c0004 | t0004 | g0147 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03098 | hp1 | a0001 | c0005 | t0006 | g0165 | AFR | MSL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | MSL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0271 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03130 | hp2 | a0001 | c0005 | t0006 | g0167 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03139 | hp1 | a0001 | c0003 | t0012 | g0038 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03195 | hp1 | a0001 | c0003 | t0011 | g0247 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | MSL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | MSL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03225 | hp1 | a0001 | c0007 | t0026 | g0109 | AFR | MSL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0250 | AFR | MSL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03239 | hp1 | a0001 | c0001 | t0018 | g0004 | SAS | PJL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0262 | SAS | PJL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0138 | AFR | MSL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03453 | hp2 | a0001 | c0005 | t0006 | g0026 | AFR | MSL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0276 | AFR | MSL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03486 | hp2 | a0001 | c0005 | t0006 | g0032 | AFR | MSL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | PJL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | PJL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03516 | hp1 | a0001 | c0001 | t0015 | g0254 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | ESN | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0260 | AFR | GWD | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03579 | hp1 | a0001 | c0001 | t0017 | g0098 | AFR | MSL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0155 | AFR | MSL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | PJL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0114 | SAS | PJL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG04199 | hp1 | a0001 | c0001 | t0007 | g0049 | SAS | STU | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | STU | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG04204 | hp1 | a0001 | c0001 | t0034 | g0174 | SAS | STU | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | STU | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | YRI | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0239 | AFR | YRI | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | CHB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18612 | hp2 | a0001 | c0001 | t0007 | g0044 | EAS | CHB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18940 | hp1 | a0001 | c0001 | t0007 | g0041 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18942 | hp1 | a0001 | c0004 | t0004 | g0107 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18944 | hp1 | a0001 | c0001 | t0009 | g0081 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18944 | hp2 | a0001 | c0003 | t0004 | g0043 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18956 | hp2 | a0001 | c0003 | t0004 | g0045 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18957 | hp2 | a0001 | c0001 | t0009 | g0080 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18963 | hp1 | a0001 | c0003 | t0004 | g0212 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18966 | hp1 | a0001 | c0004 | t0014 | g0120 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18966 | hp2 | a0001 | c0001 | t0007 | g0179 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18968 | hp2 | a0001 | c0003 | t0004 | g0008 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18971 | hp1 | a0001 | c0001 | t0009 | g0067 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18974 | hp1 | a0001 | c0001 | t0022 | g0189 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18974 | hp2 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18979 | hp2 | a0001 | c0004 | t0004 | g0144 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18981 | hp1 | a0001 | c0003 | t0004 | g0033 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18983 | hp1 | a0001 | c0003 | t0004 | g0008 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18984 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18991 | hp1 | a0001 | c0003 | t0004 | g0180 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18991 | hp2 | a0001 | c0002 | t0031 | g0140 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18993 | hp1 | a0001 | c0003 | t0004 | g0164 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18998 | hp1 | a0001 | c0003 | t0004 | g0192 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19004 | hp2 | a0001 | c0002 | t0030 | g0133 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19005 | hp1 | a0001 | c0003 | t0004 | g0199 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19007 | hp1 | a0001 | c0001 | t0007 | g0042 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19010 | hp2 | a0001 | c0001 | t0024 | g0213 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0094 | AFR | LWK | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19043 | hp2 | a0001 | c0003 | t0004 | g0171 | AFR | LWK | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19060 | hp1 | a0001 | c0004 | t0004 | g0139 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19062 | hp2 | a0001 | c0003 | t0004 | g0008 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19065 | hp1 | a0001 | c0001 | t0023 | g0184 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19065 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19068 | hp2 | a0001 | c0001 | t0009 | g0069 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19070 | hp1 | a0001 | c0003 | t0019 | g0168 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19076 | hp1 | a0001 | c0003 | t0004 | g0210 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19077 | hp2 | a0001 | c0001 | t0009 | g0095 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19081 | hp1 | a0001 | c0001 | t0009 | g0068 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19081 | hp2 | a0001 | c0003 | t0004 | g0223 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19085 | hp1 | a0001 | c0002 | t0032 | g0001 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19088 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA19090 | hp2 | a0001 | c0003 | t0020 | g0162 | EAS | JPT | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | ASW | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0240 | AFR | ASW | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0137 | EUR | TSI | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0101 | EUR | TSI | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | GIH | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0105 | SAS | GIH | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | CLM | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0267 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02109 | hp2 | a0001 | c0001 | t0013 | g0273 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02486 | hp2 | a0001 | c0003 | t0012 | g0056 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG02559 | hp2 | a0001 | c0003 | t0004 | g0152 | AFR | ACB | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | MSL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG03471 | hp2 | a0001 | c0001 | t0013 | g0277 | AFR | MSL | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | USA | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | USA | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA20300 | hp1 | a0001 | c0005 | t0006 | g0160 | AFR | USA | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0034 | AFR | USA | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0261 | AFR | LWK | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| NA21309 | hp2 | a0001 | c0003 | t0004 | g0172 | AFR | LWK | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0106 | REF | REF | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0012 | g0037 | REF | REF | SELENOI_chr2_26341143_26400885 | SELENOI | chr2 | 26341143 | 26400885 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26367216 | T | G | 2 | a0001c0002 a0001c0004 |
82 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
synonymous_variant | LOW | c.306T>G | p.Thr102Thr | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/10 | 396/8066 | 306/1194 | 102/397 | chr2 | 26367216 | |||
| chr2:26373377 | C | T | 1 | a0001c0007 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.321C>T | p.Asp107Asp | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/10 | 411/8066 | 321/1194 | 107/397 | chr2 | 26373377 | |||
| chr2:26373581 | T | C | 1 | a0001c0006 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.525T>C | p.Tyr175Tyr | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/10 | 615/8066 | 525/1194 | 175/397 | chr2 | 26373581 | |||
| chr2:26385124 | T | C | 5 | a0001c0001 a0001c0002 a0001c0005 others(2): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
synonymous_variant | LOW | c.897T>C | p.Ala299Ala | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 8/10 | 987/8066 | 897/1194 | 299/397 | chr2 | 26385124 | |||
| chr2:26389049 | G | A | 2 | a0001c0005 a0001c0006 |
7 | HG02886.hp2 HG03041.hp1 HG03098.hp1 others(4): Show |
synonymous_variant | LOW | c.1140G>A | p.Leu380Leu | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 1230/8066 | 1140/1194 | 380/397 | chr2 | 26389049 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26346198 | T | C | 1 | a0001c0004t0014 | 1 | NA18966.hp1 | 5_prime_UTR_variant | MODIFIER | c.-35T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/10 | 35 | chr2 | 26346198 | ||||||
| chr2:26389343 | A | G | 1 | a0001c0001t0035 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*240A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 240 | chr2 | 26389343 | ||||||
| chr2:26389410 | T | C | 1 | a0001c0001t0015 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*307T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 307 | chr2 | 26389410 | ||||||
| chr2:26389531 | T | C | 1 | a0001c0001t0008 | 9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*428T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 428 | chr2 | 26389531 | ||||||
| chr2:26389536 | G | A | 1 | a0001c0001t0009 | 6 | NA18944.hp1 NA18957.hp2 NA18971.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*433G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 433 | chr2 | 26389536 | ||||||
| chr2:26389566 | A | G | 3 | a0001c0001t0007 a0001c0001t0033 a0001c0001t0034 |
16 | HG00408.hp1 HG00609.hp1 HG02071.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*463A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 463 | chr2 | 26389566 | ||||||
| chr2:26389597 | G | A | 5 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0016 others(2): Show |
63 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*494G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 494 | chr2 | 26389597 | ||||||
| chr2:26389976 | C | T | 1 | a0001c0001t0034 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*873C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 873 | chr2 | 26389976 | ||||||
| chr2:26390021 | G | T | 1 | a0001c0001t0010 | 6 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*918G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 918 | chr2 | 26390021 | ||||||
| chr2:26390080 | G | A | 1 | a0001c0001t0016 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*977G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 977 | chr2 | 26390080 | ||||||
| chr2:26390188 | C | T | 38 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(35): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*1085C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 1085 | chr2 | 26390188 | ||||||
| chr2:26390461 | A | G | 3 | a0001c0002t0001 a0001c0002t0031 a0001c0002t0032 |
74 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1358A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 1358 | chr2 | 26390461 | ||||||
| chr2:26390474 | CTATT | C | 1 | a0001c0001t0008 | 9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1375_*1378delTTAT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 1375 | INFO_REALIGN_3_PRIME | chr2 | 26390474 | |||||
| chr2:26390867 | G | C | 1 | a0001c0001t0008 | 9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1764G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 1764 | chr2 | 26390867 | ||||||
| chr2:26391075 | ATT | A | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(34): Show |
324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*1975_*1976delTT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 1975 | INFO_REALIGN_3_PRIME | chr2 | 26391075 | |||||
| chr2:26391087 | C | T | 1 | a0001c0002t0030 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1984C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 1984 | chr2 | 26391087 | ||||||
| chr2:26391106 | C | T | 32 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(29): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*2003C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 2003 | chr2 | 26391106 | ||||||
| chr2:26391222 | A | C | 3 | a0001c0001t0007 a0001c0001t0033 a0001c0001t0034 |
16 | HG00408.hp1 HG00609.hp1 HG02071.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2119A>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 2119 | chr2 | 26391222 | ||||||
| chr2:26391322 | A | G | 3 | a0001c0001t0027 a0001c0001t0028 a0001c0001t0029 |
3 | HG00642.hp1 HG01109.hp2 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2219A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 2219 | chr2 | 26391322 | ||||||
| chr2:26391499 | C | T | 1 | a0001c0001t0029 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2396C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 2396 | chr2 | 26391499 | ||||||
| chr2:26391715 | T | TA | 32 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(29): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*2618dupA | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 2619 | INFO_REALIGN_3_PRIME | chr2 | 26391715 | |||||
| chr2:26391876 | A | G | 1 | a0001c0002t0032 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2773A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 2773 | chr2 | 26391876 | ||||||
| chr2:26392013 | T | C | 1 | a0001c0001t0021 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2910T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 2910 | chr2 | 26392013 | ||||||
| chr2:26392052 | A | C | 1 | a0001c0001t0008 | 9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2949A>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 2949 | chr2 | 26392052 | ||||||
| chr2:26392081 | A | G | 1 | a0001c0003t0020 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2978A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 2978 | chr2 | 26392081 | ||||||
| chr2:26392248 | T | C | 1 | a0001c0001t0008 | 9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3145T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 3145 | chr2 | 26392248 | ||||||
| chr2:26392583 | A | G | 1 | a0001c0003t0019 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3480A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 3480 | chr2 | 26392583 | ||||||
| chr2:26393034 | G | A | 6 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0016 others(3): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3931G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 3931 | chr2 | 26393034 | ||||||
| chr2:26393227 | T | C | 1 | a0001c0002t0031 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4124T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 4124 | chr2 | 26393227 | ||||||
| chr2:26393391 | T | A | 1 | a0001c0001t0023 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4288T>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 4288 | chr2 | 26393391 | ||||||
| chr2:26393488 | A | G | 6 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0016 others(3): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*4385A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 4385 | chr2 | 26393488 | ||||||
| chr2:26393533 | A | T | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(27): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*4430A>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 4430 | chr2 | 26393533 | ||||||
| chr2:26393756 | G | C | 5 | a0001c0001t0002 a0001c0001t0022 a0001c0001t0023 others(2): Show |
74 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*4653G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 4653 | chr2 | 26393756 | ||||||
| chr2:26393951 | C | T | 1 | a0001c0001t0033 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4848C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 4848 | chr2 | 26393951 | ||||||
| chr2:26394191 | C | T | 1 | a0001c0001t0018 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5088C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 5088 | chr2 | 26394191 | ||||||
| chr2:26394270 | G | A | 1 | a0001c0007t0026 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5167G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 5167 | chr2 | 26394270 | ||||||
| chr2:26394341 | A | G | 6 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0009 others(3): Show |
72 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*5238A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 5238 | chr2 | 26394341 | ||||||
| chr2:26394402 | TAATAAA | T | 2 | a0001c0001t0013 a0001c0001t0015 |
5 | HG00733.hp1 HG01167.hp1 HG02109.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5306_*5311delAATA others(2): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 5306 | INFO_REALIGN_3_PRIME | chr2 | 26394402 | |||||
| chr2:26394408 | A | T | 1 | a0001c0001t0005 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5305A>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 5305 | chr2 | 26394408 | ||||||
| chr2:26394964 | G | C | 2 | a0001c0001t0027 a0001c0001t0029 |
2 | HG00642.hp1 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5861G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 5861 | chr2 | 26394964 | ||||||
| chr2:26395329 | T | G | 1 | a0001c0001t0017 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6226T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 6226 | chr2 | 26395329 | ||||||
| chr2:26395371 | C | T | 1 | a0001c0001t0034 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6268C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 6268 | chr2 | 26395371 | ||||||
| chr2:26395521 | C | T | 7 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0013 others(4): Show |
37 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*6418C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 6418 | chr2 | 26395521 | ||||||
| chr2:26395675 | G | A | 5 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0016 others(2): Show |
63 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*6572G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 6572 | chr2 | 26395675 | ||||||
| chr2:26395692 | C | T | 3 | a0001c0001t0027 a0001c0001t0028 a0001c0001t0029 |
3 | HG00642.hp1 HG01109.hp2 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6589C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 10/10 | 6589 | chr2 | 26395692 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26346715 | G | C | 2 | a0001c0002t0001g0024 a0001c0002t0001g0025 |
2 | HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.57+426G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26346715 | |||||||
| chr2:26347104 | C | G | 41 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(38): Show |
42 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.57+815C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26347104 | |||||||
| chr2:26347350 | C | T | 2 | a0001c0002t0001g0248 a0001c0002t0001g0249 |
2 | NA18954.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.57+1061C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26347350 | |||||||
| chr2:26347435 | T | TA | 6 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(3): Show |
6 | HG01496.hp1 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+1159dupA | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26347435 | ||||||
| chr2:26347589 | A | G | 2 | a0001c0003t0011g0010 a0001c0003t0011g0247 |
4 | HG00738.hp2 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+1300A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26347589 | |||||||
| chr2:26347619 | G | T | 4 | a0001c0001t0002g0243 a0001c0001t0002g0244 a0001c0001t0002g0245 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+1330G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26347619 | |||||||
| chr2:26347645 | C | T | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+1356C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26347645 | |||||||
| chr2:26347719 | A | G | 75 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(72): Show |
86 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.57+1430A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26347719 | |||||||
| chr2:26347780 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.57+1491G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26347780 | |||||||
| chr2:26347879 | G | A | 3 | a0001c0005t0006g0026 a0001c0005t0006g0032 a0001c0006t0006g0027 |
3 | HG02886.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.57+1590G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26347879 | |||||||
| chr2:26347957 | C | A | 1 | a0001c0003t0004g0033 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.57+1668C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26347957 | |||||||
| chr2:26348020 | G | A | 1 | a0001c0001t0008g0238 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.57+1731G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26348020 | |||||||
| chr2:26348091 | T | A | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.57+1802T>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26348091 | |||||||
| chr2:26348101 | A | T | 1 | a0001c0001t0003g0175 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.57+1812A>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26348101 | |||||||
| chr2:26348206 | G | T | 1 | a0001c0001t0034g0174 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.57+1917G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26348206 | |||||||
| chr2:26348416 | C | G | 1 | a0001c0002t0001g0173 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.57+2127C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26348416 | |||||||
| chr2:26348440 | A | G | 284 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(281): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.57+2151A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26348440 | |||||||
| chr2:26348476 | C | T | 1 | a0001c0001t0034g0174 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.57+2187C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26348476 | |||||||
| chr2:26348496 | T | A | 13 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(10): Show |
16 | HG00609.hp1 HG02071.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.57+2207T>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26348496 | |||||||
| chr2:26348543 | G | A | 112 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(109): Show |
121 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.57+2254G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26348543 | |||||||
| chr2:26348578 | A | C | 3 | a0001c0001t0002g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 |
3 | HG00438.hp2 HG00673.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.57+2289A>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26348578 | |||||||
| chr2:26348581 | C | T | 2 | a0001c0003t0004g0171 a0001c0003t0004g0172 |
2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.57+2292C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26348581 | |||||||
| chr2:26348691 | CT | C | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.57+2416delT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26348691 | ||||||
| chr2:26348702 | T | C | 2 | a0001c0001t0002g0235 a0001c0001t0002g0236 |
2 | HG00673.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.57+2413T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26348702 | |||||||
| chr2:26348885 | G | A | 2 | a0001c0001t0005g0022 a0001c0001t0035g0022 |
2 | HG01106.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.57+2596G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26348885 | |||||||
| chr2:26348988 | T | C | 2 | a0001c0003t0004g0171 a0001c0003t0004g0172 |
2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.57+2699T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26348988 | |||||||
| chr2:26348996 | C | CTT | 6 | a0001c0003t0004g0169 a0001c0003t0004g0170 a0001c0003t0019g0168 others(3): Show |
6 | HG01168.hp1 HG01169.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+2741_57+2742dup others(2): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26348996 | ||||||
| chr2:26348996 | CTTT | C | 8 | a0001c0001t0008g0030 a0001c0001t0008g0239 a0001c0001t0008g0240 others(5): Show |
8 | HG00733.hp2 HG02976.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+2740_57+2742del others(3): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26348996 | ||||||
| chr2:26348996 | CTTTT | C | 25 | a0001c0001t0002g0233 a0001c0002t0001g0002 a0001c0002t0001g0014 others(22): Show |
31 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.57+2739_57+2742del others(4): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26348996 | ||||||
| chr2:26348996 | CTTTTT | C | 65 | a0001c0001t0002g0021 a0001c0001t0002g0211 a0001c0001t0002g0214 others(62): Show |
77 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.57+2738_57+2742del others(5): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26348996 | ||||||
| chr2:26348996 | CTTTTTT | C | 52 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(49): Show |
62 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.57+2737_57+2742del others(6): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26348996 | ||||||
| chr2:26348996 | CTTTTTTT | C | 27 | a0001c0001t0002g0177 a0001c0001t0002g0243 a0001c0001t0003g0086 others(24): Show |
30 | HG00735.hp2 HG01123.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.57+2736_57+2742del others(7): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26348996 | ||||||
| chr2:26348996 | CTTTTTTT others(1): Show |
C | 36 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(33): Show |
41 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.57+2735_57+2742del others(8): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26348996 | ||||||
| chr2:26348996 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0005g0287 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.57+2725_57+2742del others(18): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26348996 | ||||||
| chr2:26348996 | CTTTTTTT others(12): Show |
C | 42 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(39): Show |
43 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.57+2724_57+2742del others(19): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26348996 | ||||||
| chr2:26348996 | CTTTTTTT others(13): Show |
C | 5 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0053 others(2): Show |
5 | HG03490.hp2 HG03492.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+2723_57+2742del others(20): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26348996 | ||||||
| chr2:26349070 | C | T | 1 | a0001c0001t0027g0286 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.57+2781C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26349070 | |||||||
| chr2:26349134 | G | C | 13 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(10): Show |
16 | HG00609.hp1 HG02071.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.57+2845G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26349134 | |||||||
| chr2:26349200 | C | A | 113 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(110): Show |
122 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(119): Show |
intron_variant | MODIFIER | c.57+2911C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26349200 | |||||||
| chr2:26349308 | C | CT | 24 | a0001c0001t0003g0086 a0001c0001t0003g0102 a0001c0001t0007g0003 others(21): Show |
27 | HG00609.hp1 HG00741.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.57+3034dupT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26349308 | ||||||
| chr2:26349308 | C | CTT | 101 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(98): Show |
110 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.57+3033_57+3034dup others(2): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26349308 | ||||||
| chr2:26349369 | C | T | 2 | a0001c0001t0006g0005 a0001c0001t0006g0104 |
5 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+3080C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26349369 | |||||||
| chr2:26349452 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.57+3163G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26349452 | |||||||
| chr2:26349499 | G | A | 13 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(10): Show |
16 | HG00609.hp1 HG02071.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.57+3210G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26349499 | |||||||
| chr2:26349557 | C | T | 1 | a0001c0002t0001g0138 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.57+3268C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26349557 | |||||||
| chr2:26349670 | G | GT | 212 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(209): Show |
247 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.57+3400dupT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26349670 | ||||||
| chr2:26349670 | G | GTT | 63 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0001t0002g0232 others(60): Show |
68 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.57+3399_57+3400dup others(2): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26349670 | ||||||
| chr2:26349734 | A | G | 1 | a0001c0001t0002g0176 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.57+3445A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26349734 | |||||||
| chr2:26349735 | G | A | 1 | a0001c0002t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.57+3446G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26349735 | |||||||
| chr2:26349758 | T | C | 1 | a0001c0001t0006g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.57+3469T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26349758 | |||||||
| chr2:26349932 | C | CA | 42 | a0001c0001t0002g0178 a0001c0001t0002g0181 a0001c0001t0002g0182 others(39): Show |
44 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.57+3670dupA | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26349932 | ||||||
| chr2:26349932 | CA | C | 49 | a0001c0001t0002g0209 a0001c0001t0003g0004 a0001c0001t0003g0007 others(46): Show |
54 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.57+3670delA | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26349932 | ||||||
| chr2:26350039 | T | C | 1 | a0001c0001t0033g0046 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.57+3750T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26350039 | |||||||
| chr2:26350106 | CA | C | 38 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(35): Show |
39 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.57+3828delA | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26350106 | ||||||
| chr2:26350194 | T | TCAA | 190 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(187): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.57+3911_57+3913dup others(3): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26350194 | ||||||
| chr2:26350385 | G | A | 1 | a0001c0001t0003g0092 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.57+4096G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26350385 | |||||||
| chr2:26350397 | C | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.57+4108C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26350397 | |||||||
| chr2:26350478 | C | A | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.57+4189C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26350478 | |||||||
| chr2:26350584 | G | A | 64 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(61): Show |
82 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.57+4295G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26350584 | |||||||
| chr2:26350609 | A | C | 1 | a0001c0001t0002g0020 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.57+4320A>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26350609 | |||||||
| chr2:26350654 | A | G | 5 | a0001c0001t0010g0023 a0001c0001t0010g0255 a0001c0001t0010g0279 others(2): Show |
6 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+4365A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26350654 | |||||||
| chr2:26350733 | G | A | 5 | a0001c0004t0004g0107 a0001c0004t0004g0119 a0001c0004t0004g0139 others(2): Show |
5 | HG00558.hp2 NA18942.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+4444G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26350733 | |||||||
| chr2:26350869 | A | G | 2 | a0001c0001t0005g0022 a0001c0001t0035g0022 |
2 | HG01106.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.57+4580A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26350869 | |||||||
| chr2:26351051 | G | GT | 3 | a0001c0001t0006g0035 a0001c0001t0028g0283 a0001c0001t0029g0282 |
3 | HG00642.hp1 HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.57+4765dupT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26351051 | ||||||
| chr2:26351053 | T | TG | 4 | a0001c0001t0005g0275 a0001c0001t0005g0276 a0001c0001t0013g0277 others(1): Show |
4 | HG02647.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+4764_57+4765ins others(1): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26351053 | |||||||
| chr2:26351054 | T | G | 33 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(30): Show |
34 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.57+4765T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26351054 | |||||||
| chr2:26351055 | G | GT | 19 | a0001c0001t0003g0060 a0001c0001t0003g0085 a0001c0001t0003g0091 others(16): Show |
22 | HG01109.hp1 HG01168.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.57+4787dupT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26351055 | ||||||
| chr2:26351055 | G | T | 42 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(39): Show |
43 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.57+4766G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26351055 | |||||||
| chr2:26351055 | GT | G | 69 | a0001c0001t0003g0066 a0001c0002t0001g0001 a0001c0002t0001g0002 others(66): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.57+4787delT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26351055 | ||||||
| chr2:26351062 | T | TG | 70 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(67): Show |
81 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.57+4773_57+4774ins others(1): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26351062 | |||||||
| chr2:26351063 | T | G | 1 | a0001c0001t0002g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.57+4774T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26351063 | |||||||
| chr2:26351279 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.57+4990A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26351279 | |||||||
| chr2:26351284 | C | T | 1 | a0001c0001t0006g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.57+4995C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26351284 | |||||||
| chr2:26351452 | C | T | 1 | a0001c0001t0002g0208 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.57+5163C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26351452 | |||||||
| chr2:26351526 | T | C | 1 | a0001c0001t0006g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.57+5237T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26351526 | |||||||
| chr2:26351526 | T | G | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.57+5237T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26351526 | |||||||
| chr2:26351746 | C | A | 1 | a0001c0001t0005g0287 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.57+5457C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26351746 | |||||||
| chr2:26351761 | T | A | 1 | a0001c0001t0005g0287 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.57+5472T>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26351761 | |||||||
| chr2:26351831 | C | T | 4 | a0001c0005t0006g0160 a0001c0005t0006g0165 a0001c0005t0006g0166 others(1): Show |
4 | HG03041.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+5542C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26351831 | |||||||
| chr2:26351997 | C | T | 2 | a0001c0002t0001g0108 a0001c0002t0001g0135 |
2 | HG01081.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.57+5708C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26351997 | |||||||
| chr2:26352006 | T | C | 1 | a0001c0007t0026g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.57+5717T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26352006 | |||||||
| chr2:26352009 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.57+5720C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26352009 | |||||||
| chr2:26352044 | G | A | 3 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0256 |
3 | HG02055.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.57+5755G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26352044 | |||||||
| chr2:26352265 | C | G | 1 | a0001c0001t0002g0228 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.57+5976C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26352265 | |||||||
| chr2:26352337 | C | T | 2 | a0001c0003t0004g0171 a0001c0003t0004g0172 |
2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.57+6048C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26352337 | |||||||
| chr2:26352507 | G | A | 4 | a0001c0005t0006g0160 a0001c0005t0006g0165 a0001c0005t0006g0166 others(1): Show |
4 | HG03041.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+6218G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26352507 | |||||||
| chr2:26352568 | G | A | 75 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(72): Show |
86 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.57+6279G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26352568 | |||||||
| chr2:26352611 | C | G | 2 | a0001c0001t0003g0083 a0001c0001t0003g0084 |
2 | HG00741.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.57+6322C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26352611 | |||||||
| chr2:26352699 | G | A | 107 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(104): Show |
126 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.57+6410G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26352699 | |||||||
| chr2:26352770 | C | T | 3 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 |
3 | HG01496.hp1 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.57+6481C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26352770 | |||||||
| chr2:26352843 | G | GA | 97 | a0001c0001t0002g0178 a0001c0001t0002g0231 a0001c0001t0002g0235 others(94): Show |
118 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.57+6570dupA | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26352843 | ||||||
| chr2:26352843 | G | GAA | 7 | a0001c0001t0003g0089 a0001c0001t0007g0041 a0001c0001t0034g0174 others(4): Show |
7 | HG01175.hp2 HG01433.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+6569_57+6570dup others(2): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26352843 | ||||||
| chr2:26352843 | GA | G | 5 | a0001c0001t0002g0227 a0001c0001t0006g0005 a0001c0001t0006g0104 others(2): Show |
8 | HG02040.hp2 HG02486.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+6570delA | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26352843 | ||||||
| chr2:26353118 | A | G | 68 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(65): Show |
73 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.57+6829A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26353118 | |||||||
| chr2:26353220 | A | T | 1 | a0001c0001t0003g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.57+6931A>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26353220 | |||||||
| chr2:26353414 | G | T | 38 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(35): Show |
39 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.57+7125G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26353414 | |||||||
| chr2:26353693 | G | A | 68 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(65): Show |
73 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.57+7404G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26353693 | |||||||
| chr2:26353954 | C | A | 2 | a0001c0003t0004g0171 a0001c0003t0004g0172 |
2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.57+7665C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26353954 | |||||||
| chr2:26354200 | C | G | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.57+7911C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26354200 | |||||||
| chr2:26354313 | G | A | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.57+8024G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26354313 | |||||||
| chr2:26354435 | G | T | 3 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0097 |
3 | HG01934.hp1 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.57+8146G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26354435 | |||||||
| chr2:26354451 | A | G | 2 | a0001c0001t0006g0005 a0001c0001t0006g0104 |
5 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+8162A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26354451 | |||||||
| chr2:26354469 | C | T | 53 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(50): Show |
58 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.57+8180C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26354469 | |||||||
| chr2:26354560 | GT | G | 19 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(16): Show |
22 | HG00408.hp1 HG00609.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.57+8283delT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26354560 | ||||||
| chr2:26354601 | T | C | 18 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(15): Show |
23 | HG00609.hp1 HG00642.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.57+8312T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26354601 | |||||||
| chr2:26354612 | T | C | 1 | a0001c0001t0003g0051 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.57+8323T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26354612 | |||||||
| chr2:26354629 | G | T | 1 | a0001c0001t0003g0105 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.57+8340G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26354629 | |||||||
| chr2:26354662 | A | T | 3 | a0001c0001t0010g0255 a0001c0001t0010g0280 a0001c0001t0010g0281 |
3 | HG01891.hp2 HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.57+8373A>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26354662 | |||||||
| chr2:26354829 | G | A | 1 | a0001c0001t0003g0051 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.57+8540G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26354829 | |||||||
| chr2:26354910 | G | C | 1 | a0001c0001t0002g0185 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.57+8621G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26354910 | |||||||
| chr2:26354990 | A | T | 7 | a0001c0005t0006g0026 a0001c0005t0006g0032 a0001c0005t0006g0160 others(4): Show |
7 | HG02886.hp2 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+8701A>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26354990 | |||||||
| chr2:26354997 | G | C | 1 | a0001c0007t0026g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.57+8708G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26354997 | |||||||
| chr2:26355004 | A | G | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.57+8715A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26355004 | |||||||
| chr2:26355089 | A | G | 3 | a0001c0001t0027g0286 a0001c0001t0028g0283 a0001c0001t0029g0282 |
3 | HG00642.hp1 HG01109.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.57+8800A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26355089 | |||||||
| chr2:26355170 | C | G | 5 | a0001c0001t0013g0272 a0001c0001t0013g0273 a0001c0001t0013g0274 others(2): Show |
5 | HG00733.hp1 HG01167.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+8881C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26355170 | |||||||
| chr2:26355385 | C | CA | 68 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(65): Show |
73 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.58-8916dupA | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26355385 | ||||||
| chr2:26355536 | A | G | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.58-8766A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26355536 | |||||||
| chr2:26355658 | C | T | 1 | a0001c0002t0001g0154 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.58-8644C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26355658 | |||||||
| chr2:26355727 | GTC | G | 81 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(78): Show |
89 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.58-8560_58-8559del others(2): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26355727 | ||||||
| chr2:26355746 | T | C | 2 | a0001c0002t0001g0115 a0001c0002t0001g0116 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.58-8556T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26355746 | |||||||
| chr2:26355772 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.58-8530G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26355772 | |||||||
| chr2:26355915 | A | G | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-8387A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26355915 | |||||||
| chr2:26356159 | G | A | 4 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(1): Show |
4 | HG01496.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-8143G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26356159 | |||||||
| chr2:26356253 | G | A | 7 | a0001c0001t0003g0066 a0001c0001t0003g0070 a0001c0001t0003g0071 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-8049G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26356253 | |||||||
| chr2:26356718 | T | A | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-7584T>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26356718 | |||||||
| chr2:26356829 | T | C | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.58-7473T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26356829 | |||||||
| chr2:26356956 | C | CCA | 13 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(10): Show |
16 | HG00609.hp1 HG02071.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.58-7332_58-7331dup others(2): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26356956 | ||||||
| chr2:26356972 | G | A | 1 | a0001c0001t0008g0241 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.58-7330G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26356972 | |||||||
| chr2:26357037 | T | C | 1 | a0001c0002t0001g0122 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.58-7265T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26357037 | |||||||
| chr2:26357078 | T | TA | 42 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(39): Show |
43 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.58-7224_58-7223ins others(1): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26357078 | |||||||
| chr2:26357232 | A | G | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.58-7070A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26357232 | |||||||
| chr2:26357269 | C | T | 42 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(39): Show |
43 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.58-7033C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26357269 | |||||||
| chr2:26357573 | C | T | 3 | a0001c0001t0027g0286 a0001c0001t0028g0283 a0001c0001t0029g0282 |
3 | HG00642.hp1 HG01109.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.58-6729C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26357573 | |||||||
| chr2:26357669 | T | C | 1 | a0001c0001t0002g0186 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.58-6633T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26357669 | |||||||
| chr2:26357713 | G | A | 7 | a0001c0005t0006g0026 a0001c0005t0006g0032 a0001c0005t0006g0160 others(4): Show |
7 | HG02886.hp2 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-6589G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26357713 | |||||||
| chr2:26357715 | A | G | 1 | a0001c0002t0001g0149 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.58-6587A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26357715 | |||||||
| chr2:26357864 | C | T | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.58-6438C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26357864 | |||||||
| chr2:26357865 | G | A | 5 | a0001c0001t0013g0272 a0001c0001t0013g0273 a0001c0001t0013g0274 others(2): Show |
5 | HG00733.hp1 HG01167.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-6437G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26357865 | |||||||
| chr2:26357875 | AG | A | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.58-6424delG | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26357875 | ||||||
| chr2:26357883 | A | G | 275 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(272): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.58-6419A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26357883 | |||||||
| chr2:26357889 | A | G | 5 | a0001c0001t0010g0023 a0001c0001t0010g0255 a0001c0001t0010g0279 others(2): Show |
6 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-6413A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26357889 | |||||||
| chr2:26358150 | C | T | 64 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(61): Show |
82 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.58-6152C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26358150 | |||||||
| chr2:26358177 | A | G | 5 | a0001c0001t0002g0178 a0001c0001t0002g0204 a0001c0001t0002g0205 others(2): Show |
5 | HG00558.hp1 NA18993.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-6125A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26358177 | |||||||
| chr2:26358236 | C | G | 1 | a0001c0003t0012g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.58-6066C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26358236 | |||||||
| chr2:26358335 | C | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.58-5967C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26358335 | |||||||
| chr2:26358338 | G | C | 1 | a0001c0002t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.58-5964G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26358338 | |||||||
| chr2:26358462 | C | T | 2 | a0001c0001t0002g0203 a0001c0001t0002g0232 |
2 | NA18980.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.58-5840C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26358462 | |||||||
| chr2:26358486 | A | G | 1 | a0001c0001t0003g0060 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.58-5816A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26358486 | |||||||
| chr2:26358802 | G | C | 1 | a0001c0001t0002g0187 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.58-5500G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26358802 | |||||||
| chr2:26358884 | C | A | 7 | a0001c0005t0006g0026 a0001c0005t0006g0032 a0001c0005t0006g0160 others(4): Show |
7 | HG02886.hp2 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-5418C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26358884 | |||||||
| chr2:26358953 | G | T | 6 | a0001c0001t0005g0268 a0001c0001t0005g0269 a0001c0001t0005g0270 others(3): Show |
6 | HG01346.hp1 HG01358.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-5349G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26358953 | |||||||
| chr2:26358970 | C | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.58-5332C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26358970 | |||||||
| chr2:26359185 | A | C | 12 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(9): Show |
12 | HG00642.hp1 HG00741.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.58-5117A>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26359185 | |||||||
| chr2:26359469 | C | T | 2 | a0001c0001t0002g0225 a0001c0001t0002g0226 |
2 | HG02523.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.58-4833C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26359469 | |||||||
| chr2:26359568 | G | A | 64 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(61): Show |
82 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.58-4734G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26359568 | |||||||
| chr2:26359575 | A | G | 1 | a0001c0001t0003g0175 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.58-4727A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26359575 | |||||||
| chr2:26359610 | T | A | 1 | a0001c0002t0001g0156 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.58-4692T>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26359610 | |||||||
| chr2:26359719 | G | C | 1 | a0001c0001t0005g0257 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.58-4583G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26359719 | |||||||
| chr2:26359768 | TC | T | 6 | a0001c0001t0003g0057 a0001c0001t0003g0088 a0001c0001t0003g0096 others(3): Show |
6 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-4533delC | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26359768 | |||||||
| chr2:26359826 | G | T | 1 | a0001c0001t0007g0044 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.58-4476G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26359826 | |||||||
| chr2:26359830 | G | T | 198 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(195): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.58-4472G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26359830 | |||||||
| chr2:26360050 | A | G | 1 | a0001c0002t0001g0111 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.58-4252A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360050 | |||||||
| chr2:26360345 | C | T | 5 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0001t0002g0209 others(2): Show |
5 | NA18747.hp2 NA18981.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-3957C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360345 | |||||||
| chr2:26360400 | G | T | 5 | a0001c0002t0001g0012 a0001c0002t0001g0117 a0001c0002t0001g0118 others(2): Show |
6 | HG00639.hp1 HG00642.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-3902G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360400 | |||||||
| chr2:26360462 | G | A | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-3840G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360462 | |||||||
| chr2:26360488 | C | G | 7 | a0001c0001t0005g0252 a0001c0001t0005g0257 a0001c0001t0005g0258 others(4): Show |
7 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-3814C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360488 | |||||||
| chr2:26360504 | T | C | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.58-3798T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360504 | |||||||
| chr2:26360619 | C | T | 13 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(10): Show |
16 | HG00609.hp1 HG02071.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.58-3683C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360619 | |||||||
| chr2:26360638 | A | C | 64 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(61): Show |
82 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.58-3664A>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360638 | |||||||
| chr2:26360750 | A | G | 1 | a0001c0001t0002g0200 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.58-3552A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360750 | |||||||
| chr2:26360765 | C | T | 44 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(41): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.58-3537C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360765 | |||||||
| chr2:26360809 | C | T | 1 | a0001c0001t0034g0174 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.58-3493C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360809 | |||||||
| chr2:26360885 | A | G | 1 | a0001c0001t0003g0082 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.58-3417A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360885 | |||||||
| chr2:26360937 | C | T | 29 | a0001c0001t0005g0252 a0001c0001t0005g0253 a0001c0001t0005g0257 others(26): Show |
30 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.58-3365C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360937 | |||||||
| chr2:26360943 | G | A | 7 | a0001c0005t0006g0026 a0001c0005t0006g0032 a0001c0005t0006g0160 others(4): Show |
7 | HG02886.hp2 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-3359G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360943 | |||||||
| chr2:26360950 | T | C | 273 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(270): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.58-3352T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26360950 | |||||||
| chr2:26361072 | G | C | 75 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(72): Show |
86 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.58-3230G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361072 | |||||||
| chr2:26361076 | T | C | 71 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(68): Show |
82 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.58-3226T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361076 | |||||||
| chr2:26361086 | C | T | 44 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(41): Show |
45 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.58-3216C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361086 | |||||||
| chr2:26361102 | T | C | 1 | a0001c0001t0002g0225 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.58-3200T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361102 | |||||||
| chr2:26361166 | A | G | 2 | a0001c0003t0004g0171 a0001c0003t0004g0172 |
2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.58-3136A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361166 | |||||||
| chr2:26361168 | C | A | 1 | a0001c0002t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.58-3134C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361168 | |||||||
| chr2:26361203 | G | T | 1 | a0001c0001t0005g0271 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.58-3099G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361203 | |||||||
| chr2:26361322 | C | T | 38 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(35): Show |
39 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.58-2980C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361322 | |||||||
| chr2:26361329 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.58-2973C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361329 | |||||||
| chr2:26361439 | T | A | 114 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(111): Show |
123 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.58-2863T>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361439 | |||||||
| chr2:26361442 | T | A | 114 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(111): Show |
123 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.58-2860T>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361442 | |||||||
| chr2:26361444 | C | A | 114 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(111): Show |
123 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.58-2858C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361444 | |||||||
| chr2:26361446 | T | G | 114 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(111): Show |
123 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.58-2856T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361446 | |||||||
| chr2:26361462 | C | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.58-2840C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361462 | |||||||
| chr2:26361507 | C | T | 1 | a0001c0002t0001g0118 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.58-2795C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361507 | |||||||
| chr2:26361657 | CT | C | 8 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(5): Show |
8 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.58-2631delT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26361657 | ||||||
| chr2:26361727 | C | T | 1 | a0001c0001t0006g0104 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.58-2575C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361727 | |||||||
| chr2:26361858 | G | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.58-2444G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361858 | |||||||
| chr2:26361925 | T | C | 13 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(10): Show |
16 | HG00609.hp1 HG02071.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.58-2377T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26361925 | |||||||
| chr2:26362182 | A | G | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.58-2120A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26362182 | |||||||
| chr2:26362468 | T | C | 1 | a0001c0001t0005g0265 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.58-1834T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26362468 | |||||||
| chr2:26362481 | C | A | 1 | a0001c0001t0002g0225 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.58-1821C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26362481 | |||||||
| chr2:26362535 | TG | T | 20 | a0001c0001t0005g0252 a0001c0001t0005g0253 a0001c0001t0005g0257 others(17): Show |
21 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.58-1764delG | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26362535 | ||||||
| chr2:26362547 | G | T | 2 | a0001c0001t0006g0005 a0001c0001t0006g0104 |
5 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-1755G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26362547 | |||||||
| chr2:26362548 | A | G | 2 | a0001c0001t0006g0005 a0001c0001t0006g0104 |
5 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-1754A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26362548 | |||||||
| chr2:26362549 | T | C | 2 | a0001c0001t0006g0005 a0001c0001t0006g0104 |
5 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-1753T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26362549 | |||||||
| chr2:26362606 | C | G | 1 | a0001c0007t0026g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.58-1696C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26362606 | |||||||
| chr2:26362616 | C | T | 3 | a0001c0003t0004g0161 a0001c0003t0004g0169 a0001c0003t0004g0170 |
3 | HG01168.hp1 HG01169.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.58-1686C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26362616 | |||||||
| chr2:26362823 | A | C | 3 | a0001c0001t0027g0286 a0001c0001t0028g0283 a0001c0001t0029g0282 |
3 | HG00642.hp1 HG01109.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.58-1479A>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26362823 | |||||||
| chr2:26362916 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.58-1386G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26362916 | |||||||
| chr2:26363041 | T | C | 12 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(9): Show |
12 | HG00642.hp1 HG00741.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.58-1261T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26363041 | |||||||
| chr2:26363078 | G | A | 3 | a0001c0001t0027g0286 a0001c0001t0028g0283 a0001c0001t0029g0282 |
3 | HG00642.hp1 HG01109.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.58-1224G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26363078 | |||||||
| chr2:26363199 | G | A | 198 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(195): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.58-1103G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26363199 | |||||||
| chr2:26363341 | G | C | 71 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(68): Show |
76 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.58-961G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26363341 | |||||||
| chr2:26363344 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.58-958G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26363344 | |||||||
| chr2:26363460 | G | C | 1 | a0001c0001t0008g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.58-842G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26363460 | |||||||
| chr2:26363516 | C | T | 13 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(10): Show |
16 | HG00609.hp1 HG02071.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.58-786C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26363516 | |||||||
| chr2:26363624 | G | A | 1 | a0001c0005t0006g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.58-678G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26363624 | |||||||
| chr2:26363702 | C | G | 2 | a0001c0001t0006g0005 a0001c0001t0006g0104 |
5 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-600C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26363702 | |||||||
| chr2:26363806 | G | T | 2 | a0001c0001t0002g0225 a0001c0001t0002g0226 |
2 | HG02523.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.58-496G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26363806 | |||||||
| chr2:26363861 | C | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.58-441C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26363861 | |||||||
| chr2:26363955 | T | C | 1 | a0001c0001t0008g0241 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.58-347T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26363955 | |||||||
| chr2:26364010 | T | A | 2 | a0001c0001t0003g0053 a0001c0001t0003g0054 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.58-292T>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26364010 | |||||||
| chr2:26364036 | C | G | 3 | a0001c0001t0002g0227 a0001c0003t0004g0223 a0001c0003t0004g0234 |
3 | HG02040.hp2 HG02056.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.58-266C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26364036 | |||||||
| chr2:26364038 | T | G | 5 | a0001c0001t0008g0238 a0001c0001t0008g0239 a0001c0001t0008g0240 others(2): Show |
5 | HG00741.hp2 HG02055.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-264T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26364038 | |||||||
| chr2:26364078 | C | CT | 11 | a0001c0001t0002g0202 a0001c0001t0002g0222 a0001c0001t0002g0226 others(8): Show |
14 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.58-203dupT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26364078 | ||||||
| chr2:26364078 | CT | C | 53 | a0001c0001t0003g0063 a0001c0001t0005g0022 a0001c0001t0005g0261 others(50): Show |
53 | HG00642.hp1 HG00733.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.58-203delT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26364078 | ||||||
| chr2:26364078 | CTT | C | 71 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(68): Show |
77 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.58-204_58-203delTT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26364078 | ||||||
| chr2:26364078 | CTTTTTTT others(5): Show |
C | 1 | a0001c0005t0006g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.58-214_58-203delTT others(10): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 26364078 | ||||||
| chr2:26364079 | T | C | 11 | a0001c0001t0002g0243 a0001c0001t0002g0244 a0001c0001t0002g0245 others(8): Show |
11 | HG01167.hp2 HG01169.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-223T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26364079 | |||||||
| chr2:26364091 | T | C | 1 | a0001c0005t0006g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.58-211T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26364091 | |||||||
| chr2:26364108 | G | A | 13 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(10): Show |
16 | HG00609.hp1 HG02071.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.58-194G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26364108 | |||||||
| chr2:26364116 | T | C | 12 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(9): Show |
12 | HG00642.hp1 HG00741.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.58-186T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26364116 | |||||||
| chr2:26364208 | G | A | 63 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(60): Show |
81 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.58-94G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 1/9 | chr2 | 26364208 | |||||||
| chr2:26365333 | C | G | 1 | a0001c0001t0034g0174 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.235+393C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26365333 | |||||||
| chr2:26365492 | C | T | 75 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(72): Show |
86 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.235+552C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26365492 | |||||||
| chr2:26365669 | G | A | 3 | a0001c0002t0001g0014 a0001c0002t0001g0110 a0001c0002t0001g0111 |
4 | HG00280.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+729G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26365669 | |||||||
| chr2:26365743 | C | T | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.235+803C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26365743 | |||||||
| chr2:26365769 | A | G | 2 | a0001c0001t0007g0179 a0001c0001t0007g0183 |
2 | HG00408.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.235+829A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26365769 | |||||||
| chr2:26365795 | C | CT | 8 | a0001c0001t0002g0182 a0001c0001t0002g0197 a0001c0001t0002g0198 others(5): Show |
8 | HG01978.hp1 HG02074.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+879dupT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 26365795 | ||||||
| chr2:26365795 | CT | C | 22 | a0001c0001t0002g0176 a0001c0001t0002g0187 a0001c0001t0002g0188 others(19): Show |
25 | HG01081.hp2 HG01168.hp1 HG02080.hp1 others(22): Show |
intron_variant | MODIFIER | c.235+879delT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 26365795 | ||||||
| chr2:26365795 | CTT | C | 10 | a0001c0001t0003g0062 a0001c0001t0006g0034 a0001c0001t0008g0238 others(7): Show |
10 | HG00642.hp1 HG00741.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+878_235+879del others(2): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 26365795 | ||||||
| chr2:26365795 | CTTT | C | 100 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(97): Show |
109 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(106): Show |
intron_variant | MODIFIER | c.235+877_235+879del others(3): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 26365795 | ||||||
| chr2:26365795 | CTTTT | C | 6 | a0001c0001t0003g0075 a0001c0001t0003g0083 a0001c0001t0008g0028 others(3): Show |
6 | HG01074.hp2 HG01496.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+876_235+879del others(4): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 26365795 | ||||||
| chr2:26365795 | CTTTTTTT others(4): Show |
C | 64 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(61): Show |
82 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.235+869_235+879del others(11): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 26365795 | ||||||
| chr2:26365947 | G | A | 2 | a0001c0001t0002g0222 a0001c0001t0002g0229 |
2 | HG00673.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.235+1007G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26365947 | |||||||
| chr2:26366018 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.235+1078C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26366018 | |||||||
| chr2:26366027 | C | G | 4 | a0001c0001t0003g0051 a0001c0001t0003g0061 a0001c0001t0003g0090 others(1): Show |
4 | HG02615.hp1 HG02630.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+1087C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26366027 | |||||||
| chr2:26366114 | C | G | 16 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(13): Show |
16 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.236-1032C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26366114 | |||||||
| chr2:26366218 | G | A | 39 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(36): Show |
44 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.236-928G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26366218 | |||||||
| chr2:26366607 | T | C | 68 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(65): Show |
73 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.236-539T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26366607 | |||||||
| chr2:26366661 | A | G | 13 | a0001c0001t0005g0022 a0001c0001t0005g0261 a0001c0001t0005g0262 others(10): Show |
13 | HG01106.hp1 HG01346.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.236-485A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26366661 | |||||||
| chr2:26366696 | T | C | 2 | a0001c0003t0011g0010 a0001c0003t0011g0247 |
4 | HG00738.hp2 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-450T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26366696 | |||||||
| chr2:26366708 | T | C | 1 | a0001c0001t0034g0174 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.236-438T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26366708 | |||||||
| chr2:26366711 | A | G | 6 | a0001c0001t0005g0268 a0001c0001t0005g0269 a0001c0001t0005g0270 others(3): Show |
6 | HG01346.hp1 HG01358.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.236-435A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26366711 | |||||||
| chr2:26366846 | T | C | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.236-300T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26366846 | |||||||
| chr2:26367006 | G | A | 1 | a0001c0001t0003g0061 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.236-140G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 3/9 | chr2 | 26367006 | |||||||
| chr2:26367250 | C | T | 64 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(61): Show |
82 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.310+30C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26367250 | |||||||
| chr2:26367659 | C | A | 54 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(51): Show |
72 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.310+439C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26367659 | |||||||
| chr2:26367761 | C | T | 81 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(78): Show |
92 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.310+541C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26367761 | |||||||
| chr2:26368033 | A | G | 2 | a0001c0002t0001g0115 a0001c0002t0001g0116 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.310+813A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26368033 | |||||||
| chr2:26368039 | G | A | 1 | a0001c0001t0003g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.310+819G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26368039 | |||||||
| chr2:26368147 | A | G | 1 | a0001c0001t0002g0219 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.310+927A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26368147 | |||||||
| chr2:26368420 | T | C | 4 | a0001c0002t0001g0113 a0001c0002t0001g0124 a0001c0002t0001g0125 others(1): Show |
4 | HG01981.hp2 HG02004.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.310+1200T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26368420 | |||||||
| chr2:26368506 | G | A | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.310+1286G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26368506 | |||||||
| chr2:26368723 | G | A | 4 | a0001c0001t0003g0051 a0001c0001t0003g0061 a0001c0001t0003g0090 others(1): Show |
4 | HG02615.hp1 HG02630.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.310+1503G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26368723 | |||||||
| chr2:26368835 | G | T | 13 | a0001c0001t0005g0022 a0001c0001t0005g0261 a0001c0001t0005g0262 others(10): Show |
13 | HG01106.hp1 HG01346.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.310+1615G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26368835 | |||||||
| chr2:26368975 | C | G | 1 | a0001c0001t0003g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.310+1755C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26368975 | |||||||
| chr2:26369159 | C | G | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.310+1939C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26369159 | |||||||
| chr2:26369182 | G | T | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.310+1962G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26369182 | |||||||
| chr2:26369377 | A | G | 7 | a0001c0005t0006g0026 a0001c0005t0006g0032 a0001c0005t0006g0160 others(4): Show |
7 | HG02886.hp2 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.310+2157A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26369377 | |||||||
| chr2:26369485 | T | G | 2 | a0001c0003t0011g0010 a0001c0003t0011g0247 |
4 | HG00738.hp2 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+2265T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26369485 | |||||||
| chr2:26369561 | T | C | 114 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(111): Show |
123 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.310+2341T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26369561 | |||||||
| chr2:26369582 | C | A | 1 | a0001c0001t0003g0074 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.310+2362C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26369582 | |||||||
| chr2:26369637 | G | T | 1 | a0001c0002t0001g0016 | 2 | HG00099.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.310+2417G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26369637 | |||||||
| chr2:26369653 | A | G | 284 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(281): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.310+2433A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26369653 | |||||||
| chr2:26369666 | T | G | 57 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(54): Show |
75 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.310+2446T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26369666 | |||||||
| chr2:26369818 | A | G | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.310+2598A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26369818 | |||||||
| chr2:26369929 | A | G | 287 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(284): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.310+2709A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26369929 | |||||||
| chr2:26370003 | T | C | 114 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(111): Show |
123 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.310+2783T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370003 | |||||||
| chr2:26370022 | T | G | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.310+2802T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370022 | |||||||
| chr2:26370213 | T | C | 1 | a0001c0001t0003g0076 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.310+2993T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370213 | |||||||
| chr2:26370256 | C | T | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.310+3036C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370256 | |||||||
| chr2:26370315 | C | G | 19 | a0001c0001t0002g0178 a0001c0001t0002g0182 a0001c0001t0002g0186 others(16): Show |
19 | HG00558.hp1 HG00673.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.311-3052C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370315 | |||||||
| chr2:26370344 | A | T | 1 | a0001c0007t0026g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.311-3023A>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370344 | |||||||
| chr2:26370447 | ACCCCTCA others(610): Show |
A | 1 | a0001c0001t0003g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.311-2890_311-2274d others(2): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26370447 | ||||||
| chr2:26370464 | C | T | 13 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(10): Show |
16 | HG00609.hp1 HG02071.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.311-2903C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370464 | |||||||
| chr2:26370469 | C | T | 1 | a0001c0007t0026g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.311-2898C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370469 | |||||||
| chr2:26370470 | G | A | 57 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(54): Show |
75 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.311-2897G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370470 | |||||||
| chr2:26370477 | T | C | 1 | a0001c0001t0027g0286 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.311-2890T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370477 | |||||||
| chr2:26370482 | GGGGGGCT others(119): Show |
G | 66 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(63): Show |
69 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.311-2763_311-2638d others(2): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26370482 | ||||||
| chr2:26370514 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.311-2853G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370514 | |||||||
| chr2:26370526 | C | T | 75 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(72): Show |
86 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.311-2841C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370526 | |||||||
| chr2:26370576 | CCCTCACC others(209): Show |
C | 2 | a0001c0001t0003g0007 a0001c0001t0016g0079 |
3 | HG01255.hp2 HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.311-2763_311-2548d others(2): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26370576 | ||||||
| chr2:26370604 | T | C | 3 | a0001c0001t0027g0286 a0001c0001t0028g0283 a0001c0001t0029g0282 |
3 | HG00642.hp1 HG01109.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.311-2763T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370604 | |||||||
| chr2:26370608 | C | A | 2 | a0001c0001t0010g0023 a0001c0001t0010g0279 |
3 | HG01069.hp1 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.311-2759C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370608 | |||||||
| chr2:26370608 | C | CG | 212 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(209): Show |
247 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.311-2754dupG | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26370608 | ||||||
| chr2:26370645 | G | A | 1 | a0001c0002t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.311-2722G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370645 | |||||||
| chr2:26370646 | G | A | 2 | a0001c0003t0004g0152 a0001c0003t0004g0153 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.311-2721G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370646 | |||||||
| chr2:26370652 | C | T | 57 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(54): Show |
75 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.311-2715C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370652 | |||||||
| chr2:26370653 | G | T | 2 | a0001c0001t0007g0179 a0001c0001t0007g0183 |
2 | HG00408.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.311-2714G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370653 | |||||||
| chr2:26370685 | C | T | 7 | a0001c0005t0006g0026 a0001c0005t0006g0032 a0001c0005t0006g0160 others(4): Show |
7 | HG02886.hp2 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.311-2682C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370685 | |||||||
| chr2:26370689 | C | T | 1 | a0001c0001t0007g0049 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.311-2678C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370689 | |||||||
| chr2:26370699 | C | A | 1 | a0001c0001t0002g0221 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.311-2668C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370699 | |||||||
| chr2:26370699 | C | T | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.311-2668C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370699 | |||||||
| chr2:26370702 | CCCTCACC others(83): Show |
C | 1 | a0001c0007t0026g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.311-2621_311-2532d others(92): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26370702 | ||||||
| chr2:26370753 | C | T | 1 | a0001c0001t0005g0275 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.311-2614C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370753 | |||||||
| chr2:26370756 | CCCTCCCG others(34): Show |
C | 1 | a0001c0001t0002g0198 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.311-2583_311-2543d others(43): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26370756 | ||||||
| chr2:26370779 | C | T | 4 | a0001c0001t0002g0243 a0001c0001t0002g0244 a0001c0001t0002g0245 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-2588C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370779 | |||||||
| chr2:26370793 | C | G | 1 | a0001c0001t0016g0079 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.311-2574C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370793 | |||||||
| chr2:26370797 | A | ACCTCCCG others(42): Show |
2 | a0001c0005t0006g0026 a0001c0006t0006g0027 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.311-2546_311-2498d others(51): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26370797 | ||||||
| chr2:26370813 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.311-2554G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370813 | |||||||
| chr2:26370816 | T | C | 1 | a0001c0001t0003g0105 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.311-2551T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370816 | |||||||
| chr2:26370820 | C | T | 1 | a0001c0007t0026g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.311-2547C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370820 | |||||||
| chr2:26370821 | GGGCGGGG others(42): Show |
G | 1 | a0001c0004t0004g0147 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.311-2497_311-2449d others(51): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26370821 | ||||||
| chr2:26370836 | A | C | 2 | a0001c0001t0003g0007 a0001c0001t0016g0079 |
3 | HG01255.hp2 HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.311-2531A>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370836 | |||||||
| chr2:26370852 | C | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0181 |
5 | NA18964.hp2 NA18971.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.311-2515C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370852 | |||||||
| chr2:26370868 | CCAGGCGG others(267): Show |
C | 1 | a0001c0001t0002g0221 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.311-2497_311-2224d others(2): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26370868 | ||||||
| chr2:26370870 | A | G | 13 | a0001c0002t0005g0159 a0001c0003t0004g0033 a0001c0003t0004g0161 others(10): Show |
13 | HG00558.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.311-2497A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370870 | |||||||
| chr2:26370870 | AGGCGGGG others(91): Show |
A | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.311-2482_311-2385d others(100): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26370870 | ||||||
| chr2:26370874 | G | A | 14 | a0001c0002t0005g0159 a0001c0003t0004g0033 a0001c0003t0004g0161 others(11): Show |
14 | HG00558.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.311-2493G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370874 | |||||||
| chr2:26370895 | CCCTCCCG others(41): Show |
C | 1 | a0001c0002t0001g0131 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.311-2469_311-2422d others(50): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26370895 | ||||||
| chr2:26370905 | CGGGGCGG others(42): Show |
C | 55 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(52): Show |
73 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.311-2413_311-2365d others(51): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26370905 | ||||||
| chr2:26370922 | C | T | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.311-2445C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370922 | |||||||
| chr2:26370923 | GGGGGGCT others(41): Show |
G | 1 | a0001c0002t0001g0141 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.311-2438_311-2391d others(50): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26370923 | ||||||
| chr2:26370954 | T | C | 1 | a0001c0002t0001g0131 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.311-2413T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370954 | |||||||
| chr2:26370971 | C | T | 2 | a0001c0001t0006g0005 a0001c0001t0006g0104 |
5 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.311-2396C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26370971 | |||||||
| chr2:26371084 | G | C | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.311-2283G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371084 | |||||||
| chr2:26371113 | C | A | 2 | a0001c0003t0011g0010 a0001c0003t0011g0247 |
4 | HG00738.hp2 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-2254C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371113 | |||||||
| chr2:26371142 | G | C | 288 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(285): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.311-2225G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371142 | |||||||
| chr2:26371159 | C | T | 41 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(38): Show |
42 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.311-2208C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371159 | |||||||
| chr2:26371192 | C | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.311-2175C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371192 | |||||||
| chr2:26371193 | G | A | 42 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(39): Show |
43 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.311-2174G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371193 | |||||||
| chr2:26371251 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.311-2116C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371251 | |||||||
| chr2:26371270 | G | A | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.311-2097G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371270 | |||||||
| chr2:26371281 | C | T | 4 | a0001c0005t0006g0160 a0001c0005t0006g0165 a0001c0005t0006g0166 others(1): Show |
4 | HG03041.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.311-2086C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371281 | |||||||
| chr2:26371297 | C | CG | 16 | a0001c0001t0002g0214 a0001c0001t0002g0220 a0001c0001t0002g0225 others(13): Show |
16 | HG00438.hp2 HG01071.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.311-2066dupG | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26371297 | ||||||
| chr2:26371309 | C | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.311-2058C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371309 | |||||||
| chr2:26371331 | C | A | 1 | a0001c0001t0003g0074 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.311-2036C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371331 | |||||||
| chr2:26371395 | C | G | 3 | a0001c0001t0005g0263 a0001c0001t0005g0278 a0001c0001t0021g0264 |
3 | HG02622.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.311-1972C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371395 | |||||||
| chr2:26371642 | C | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.311-1725C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371642 | |||||||
| chr2:26371667 | C | T | 3 | a0001c0001t0003g0051 a0001c0001t0003g0061 a0001c0001t0003g0090 |
3 | HG02615.hp1 HG02630.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.311-1700C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371667 | |||||||
| chr2:26371726 | C | T | 1 | a0001c0007t0026g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.311-1641C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371726 | |||||||
| chr2:26371786 | A | G | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.311-1581A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371786 | |||||||
| chr2:26371844 | GACCATGG others(10): Show |
G | 1 | a0001c0002t0001g0146 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.311-1506_311-1490d others(19): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26371844 | ||||||
| chr2:26371861 | AACCATGG others(10): Show |
A | 2 | a0001c0001t0006g0005 a0001c0001t0006g0104 |
5 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.311-1487_311-1471d others(19): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26371861 | ||||||
| chr2:26371884 | G | GGGGAGAG others(5): Show |
1 | a0001c0002t0001g0173 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.311-1465_311-1454d others(14): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 26371884 | ||||||
| chr2:26371915 | G | A | 5 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0001c0001t0005g0259 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.311-1452G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26371915 | |||||||
| chr2:26372141 | T | G | 3 | a0001c0003t0004g0161 a0001c0003t0004g0169 a0001c0003t0004g0170 |
3 | HG01168.hp1 HG01169.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.311-1226T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26372141 | |||||||
| chr2:26372203 | C | T | 1 | a0001c0001t0021g0264 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.311-1164C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26372203 | |||||||
| chr2:26372265 | A | G | 38 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(35): Show |
43 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.311-1102A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26372265 | |||||||
| chr2:26372369 | C | G | 2 | a0001c0001t0003g0086 a0001c0001t0003g0101 |
2 | HG02145.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.311-998C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26372369 | |||||||
| chr2:26372370 | G | A | 1 | a0001c0002t0001g0131 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.311-997G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26372370 | |||||||
| chr2:26372520 | A | G | 15 | a0001c0001t0002g0009 a0001c0001t0002g0017 a0001c0001t0002g0018 others(12): Show |
19 | HG00609.hp2 HG01081.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.311-847A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26372520 | |||||||
| chr2:26372629 | G | A | 13 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(10): Show |
16 | HG00609.hp1 HG02071.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.311-738G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26372629 | |||||||
| chr2:26372898 | T | A | 1 | a0001c0002t0001g0126 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.311-469T>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26372898 | |||||||
| chr2:26372935 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.311-432C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26372935 | |||||||
| chr2:26373182 | C | T | 14 | a0001c0002t0005g0159 a0001c0003t0004g0033 a0001c0003t0004g0161 others(11): Show |
14 | HG00558.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.311-185C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26373182 | |||||||
| chr2:26373226 | T | C | 2 | a0001c0001t0006g0005 a0001c0001t0006g0104 |
5 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.311-141T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26373226 | |||||||
| chr2:26373307 | A | G | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.311-60A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 4/9 | chr2 | 26373307 | |||||||
| chr2:26373708 | T | C | 1 | a0001c0001t0003g0057 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.573+79T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | chr2 | 26373708 | |||||||
| chr2:26373859 | C | G | 2 | a0001c0001t0006g0005 a0001c0001t0006g0104 |
5 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+230C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | chr2 | 26373859 | |||||||
| chr2:26374012 | G | A | 1 | a0001c0002t0001g0012 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.573+383G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | chr2 | 26374012 | |||||||
| chr2:26374047 | C | T | 57 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(54): Show |
75 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.573+418C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | chr2 | 26374047 | |||||||
| chr2:26374048 | G | A | 11 | a0001c0001t0002g0185 a0001c0001t0002g0187 a0001c0001t0002g0190 others(8): Show |
11 | HG00438.hp2 HG00544.hp1 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.573+419G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | chr2 | 26374048 | |||||||
| chr2:26374191 | A | G | 5 | a0001c0001t0003g0066 a0001c0001t0003g0071 a0001c0001t0003g0072 others(2): Show |
5 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+562A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | chr2 | 26374191 | |||||||
| chr2:26374525 | A | G | 7 | a0001c0005t0006g0026 a0001c0005t0006g0032 a0001c0005t0006g0160 others(4): Show |
7 | HG02886.hp2 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-515A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | chr2 | 26374525 | |||||||
| chr2:26374566 | A | AT | 82 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(79): Show |
96 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.574-455dupT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 26374566 | ||||||
| chr2:26374566 | A | ATT | 10 | a0001c0001t0002g0198 a0001c0001t0002g0232 a0001c0001t0002g0237 others(7): Show |
10 | HG00438.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.574-456_574-455dup others(2): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 26374566 | ||||||
| chr2:26374566 | A | T | 4 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(1): Show |
4 | HG01496.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-474A>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | chr2 | 26374566 | |||||||
| chr2:26374566 | AT | A | 63 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(60): Show |
68 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.574-455delT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 26374566 | ||||||
| chr2:26374709 | C | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.574-331C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | chr2 | 26374709 | |||||||
| chr2:26374725 | C | T | 13 | a0001c0001t0005g0022 a0001c0001t0005g0261 a0001c0001t0005g0262 others(10): Show |
13 | HG01106.hp1 HG01346.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.574-315C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | chr2 | 26374725 | |||||||
| chr2:26374749 | G | A | 59 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(56): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.574-291G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | chr2 | 26374749 | |||||||
| chr2:26374968 | A | G | 5 | a0001c0001t0013g0272 a0001c0001t0013g0273 a0001c0001t0013g0274 others(2): Show |
5 | HG00733.hp1 HG01167.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.574-72A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | chr2 | 26374968 | |||||||
| chr2:26375012 | T | A | 2 | a0001c0001t0002g0225 a0001c0001t0002g0226 |
2 | HG02523.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.574-28T>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 5/9 | chr2 | 26375012 | |||||||
| chr2:26375696 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.682+548G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26375696 | |||||||
| chr2:26375781 | T | C | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.682+633T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26375781 | |||||||
| chr2:26375949 | A | G | 2 | a0001c0001t0008g0239 a0001c0001t0008g0240 |
2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.682+801A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26375949 | |||||||
| chr2:26376034 | G | A | 1 | a0001c0001t0005g0261 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.682+886G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26376034 | |||||||
| chr2:26376091 | C | CA | 80 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(77): Show |
91 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.682+961dupA | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26376091 | ||||||
| chr2:26376091 | CA | C | 28 | a0001c0001t0003g0054 a0001c0001t0003g0059 a0001c0001t0005g0270 others(25): Show |
28 | HG00741.hp2 HG01074.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.682+961delA | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26376091 | ||||||
| chr2:26376115 | A | T | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.682+967A>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26376115 | |||||||
| chr2:26376157 | G | A | 3 | a0001c0001t0002g0177 a0001c0001t0002g0197 a0001c0001t0002g0198 |
3 | NA18956.hp1 NA18984.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.682+1009G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26376157 | |||||||
| chr2:26376614 | AG | A | 3 | a0001c0001t0006g0005 a0001c0001t0006g0104 a0001c0001t0008g0030 |
6 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.682+1467delG | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26376614 | |||||||
| chr2:26376632 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.682+1484C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26376632 | |||||||
| chr2:26376724 | G | A | 1 | a0001c0001t0003g0085 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.682+1576G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26376724 | |||||||
| chr2:26376970 | G | A | 63 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(60): Show |
68 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.682+1822G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26376970 | |||||||
| chr2:26377358 | G | A | 56 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(53): Show |
74 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.682+2210G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26377358 | |||||||
| chr2:26377827 | G | C | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.682+2679G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26377827 | |||||||
| chr2:26377874 | T | G | 6 | a0001c0001t0006g0005 a0001c0001t0006g0104 a0001c0001t0007g0041 others(3): Show |
9 | HG00609.hp1 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.682+2726T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26377874 | |||||||
| chr2:26377878 | T | C | 1 | a0001c0003t0012g0036 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.682+2730T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26377878 | |||||||
| chr2:26378031 | G | C | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.682+2883G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26378031 | |||||||
| chr2:26378166 | C | T | 1 | a0001c0002t0001g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.682+3018C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26378166 | |||||||
| chr2:26378289 | G | A | 42 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(39): Show |
43 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.682+3141G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26378289 | |||||||
| chr2:26378359 | C | T | 42 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(39): Show |
43 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.682+3211C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26378359 | |||||||
| chr2:26378388 | T | C | 2 | a0001c0003t0011g0010 a0001c0003t0011g0247 |
4 | HG00738.hp2 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+3240T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26378388 | |||||||
| chr2:26378446 | C | T | 7 | a0001c0005t0006g0026 a0001c0005t0006g0032 a0001c0005t0006g0160 others(4): Show |
7 | HG02886.hp2 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+3298C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26378446 | |||||||
| chr2:26378513 | A | G | 1 | a0001c0002t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.682+3365A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26378513 | |||||||
| chr2:26378533 | T | C | 1 | a0001c0007t0026g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.682+3385T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26378533 | |||||||
| chr2:26378581 | A | G | 11 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(8): Show |
14 | HG00609.hp1 HG02071.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.682+3433A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26378581 | |||||||
| chr2:26378616 | CA | C | 11 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(8): Show |
14 | HG00609.hp1 HG02071.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.682+3469delA | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26378616 | |||||||
| chr2:26378619 | G | A | 38 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(35): Show |
43 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.682+3471G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26378619 | |||||||
| chr2:26378734 | AT | A | 56 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(53): Show |
74 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.682+3591delT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26378734 | ||||||
| chr2:26379120 | C | T | 1 | a0001c0001t0009g0081 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.682+3972C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26379120 | |||||||
| chr2:26379174 | G | T | 2 | a0001c0001t0003g0059 a0001c0001t0003g0091 |
2 | HG01074.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.682+4026G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26379174 | |||||||
| chr2:26379306 | T | G | 1 | a0001c0002t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.683-3993T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26379306 | |||||||
| chr2:26379362 | T | C | 1 | a0001c0001t0006g0251 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.683-3937T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26379362 | |||||||
| chr2:26379394 | C | T | 56 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(53): Show |
74 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.683-3905C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26379394 | |||||||
| chr2:26379429 | A | T | 2 | a0001c0001t0003g0011 a0001c0001t0003g0093 |
3 | HG01069.hp2 HG01123.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.683-3870A>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26379429 | |||||||
| chr2:26379494 | G | A | 39 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(36): Show |
40 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.683-3805G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26379494 | |||||||
| chr2:26379564 | C | T | 72 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(69): Show |
81 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.683-3735C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26379564 | |||||||
| chr2:26379602 | G | GTA | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.683-3681_683-3680d others(4): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26379602 | ||||||
| chr2:26379747 | A | G | 1 | a0001c0002t0001g0158 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.683-3552A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26379747 | |||||||
| chr2:26379758 | A | G | 1 | a0001c0002t0030g0133 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.683-3541A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26379758 | |||||||
| chr2:26379999 | G | A | 1 | a0001c0001t0002g0190 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.683-3300G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26379999 | |||||||
| chr2:26380014 | G | A | 1 | a0001c0007t0026g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.683-3285G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26380014 | |||||||
| chr2:26380121 | C | T | 65 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(62): Show |
74 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.683-3178C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26380121 | |||||||
| chr2:26380300 | TACTATA | T | 4 | a0001c0001t0002g0243 a0001c0001t0002g0244 a0001c0001t0002g0245 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-2997_683-2992d others(8): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26380300 | ||||||
| chr2:26380302 | C | A | 1 | a0001c0001t0005g0261 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.683-2997C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26380302 | |||||||
| chr2:26380384 | T | G | 13 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(10): Show |
16 | HG00408.hp1 HG00609.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.683-2915T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26380384 | |||||||
| chr2:26380480 | C | T | 1 | a0001c0007t0026g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.683-2819C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26380480 | |||||||
| chr2:26380616 | T | C | 1 | a0001c0002t0001g0134 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.683-2683T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26380616 | |||||||
| chr2:26380787 | G | A | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.683-2512G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26380787 | |||||||
| chr2:26380800 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.683-2499C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26380800 | |||||||
| chr2:26380893 | T | A | 2 | a0001c0001t0003g0060 a0001c0001t0003g0089 |
2 | HG01168.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.683-2406T>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26380893 | |||||||
| chr2:26380957 | A | G | 1 | a0001c0001t0002g0211 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.683-2342A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26380957 | |||||||
| chr2:26381020 | TTGA | T | 10 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0176 others(7): Show |
12 | HG01081.hp2 HG01192.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.683-2277_683-2275d others(5): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381020 | ||||||
| chr2:26381198 | C | CTT | 10 | a0001c0001t0002g0243 a0001c0001t0002g0244 a0001c0001t0002g0245 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-2071_683-2070d others(4): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTT | 6 | a0001c0001t0008g0028 a0001c0001t0008g0030 a0001c0001t0008g0031 others(3): Show |
6 | HG02055.hp2 HG02572.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-2072_683-2070d others(5): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTT | 28 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0021 others(25): Show |
34 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.683-2073_683-2070d others(6): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTT | 24 | a0001c0001t0002g0017 a0001c0001t0002g0019 a0001c0001t0002g0176 others(21): Show |
25 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.683-2074_683-2070d others(7): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTTT | 9 | a0001c0001t0002g0018 a0001c0001t0002g0020 a0001c0001t0002g0207 others(6): Show |
11 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.683-2075_683-2070d others(8): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0013g0272 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.683-2079_683-2070d others(12): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0013g0274 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.683-2080_683-2070d others(13): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0013g0273 a0001c0001t0013g0277 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.683-2081_683-2070d others(14): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTTTT others(6): Show |
4 | a0001c0001t0005g0253 a0001c0001t0006g0250 a0001c0001t0006g0256 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-2082_683-2070d others(15): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0005g0266 a0001c0001t0005g0267 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.683-2083_683-2070d others(16): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTTTT others(8): Show |
3 | a0001c0001t0005g0259 a0001c0001t0005g0276 a0001c0001t0005g0287 |
3 | HG02622.hp1 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.683-2084_683-2070d others(17): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTTTT others(9): Show |
3 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0001c0001t0006g0251 |
3 | HG01884.hp1 HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.683-2085_683-2070d others(18): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0010g0280 a0001c0001t0010g0281 |
2 | HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.683-2086_683-2070d others(19): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0010g0023 a0001c0001t0010g0255 |
3 | HG01069.hp1 HG01071.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.683-2087_683-2070d others(20): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0010g0279 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.683-2088_683-2070d others(21): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0005g0260 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.683-2090_683-2070d others(23): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0005g0252 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.683-2094_683-2070d others(27): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0005g0265 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.683-2095_683-2070d others(28): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | CT | C | 32 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0052 others(29): Show |
35 | HG00099.hp1 HG00735.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.683-2070delT | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | CTT | C | 13 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0059 others(10): Show |
13 | HG01074.hp1 HG01515.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.683-2071_683-2070d others(4): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | CTTTT | C | 8 | a0001c0001t0005g0275 a0001c0001t0027g0286 a0001c0002t0001g0012 others(5): Show |
9 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.683-2073_683-2070d others(6): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | CTTTTT | C | 27 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(24): Show |
30 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.683-2074_683-2070d others(7): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | CTTTTTT | C | 38 | a0001c0001t0003g0060 a0001c0001t0003g0089 a0001c0002t0001g0001 others(35): Show |
55 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.683-2075_683-2070d others(8): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | CTTTTTTT | C | 26 | a0001c0001t0005g0269 a0001c0001t0024g0213 a0001c0002t0001g0113 others(23): Show |
28 | HG00558.hp2 HG01168.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.683-2076_683-2070d others(9): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | CTTTTTTT others(1): Show |
C | 16 | a0001c0001t0005g0022 a0001c0001t0005g0261 a0001c0001t0005g0262 others(13): Show |
19 | HG01106.hp1 HG01346.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.683-2077_683-2070d others(10): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0008g0242 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.683-2079_683-2070d others(12): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381198 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0023g0184 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.683-2081_683-2070d others(14): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26381198 | ||||||
| chr2:26381271 | A | G | 2 | a0001c0001t0003g0083 a0001c0001t0003g0084 |
2 | HG00741.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.683-2028A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26381271 | |||||||
| chr2:26381445 | C | T | 13 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(10): Show |
16 | HG00408.hp1 HG00609.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.683-1854C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26381445 | |||||||
| chr2:26381446 | G | A | 1 | a0001c0001t0029g0282 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.683-1853G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26381446 | |||||||
| chr2:26381475 | C | T | 1 | a0001c0001t0003g0105 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.683-1824C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26381475 | |||||||
| chr2:26381609 | A | G | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.683-1690A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26381609 | |||||||
| chr2:26381658 | G | A | 1 | a0001c0001t0005g0268 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.683-1641G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26381658 | |||||||
| chr2:26381743 | G | T | 2 | a0001c0001t0006g0005 a0001c0001t0006g0104 |
5 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-1556G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26381743 | |||||||
| chr2:26381835 | A | T | 3 | a0001c0001t0005g0022 a0001c0001t0005g0262 a0001c0001t0035g0022 |
3 | HG01106.hp1 HG01928.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.683-1464A>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26381835 | |||||||
| chr2:26382040 | A | G | 1 | a0001c0001t0009g0095 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.683-1259A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26382040 | |||||||
| chr2:26382066 | G | A | 1 | a0001c0002t0001g0141 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.683-1233G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26382066 | |||||||
| chr2:26382071 | A | C | 66 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(63): Show |
75 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.683-1228A>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26382071 | |||||||
| chr2:26382247 | A | G | 8 | a0001c0003t0004g0043 a0001c0003t0004g0045 a0001c0004t0004g0107 others(5): Show |
8 | HG00558.hp2 HG03041.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-1052A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26382247 | |||||||
| chr2:26382270 | T | C | 3 | a0001c0001t0002g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 |
3 | HG00438.hp2 HG00673.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.683-1029T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26382270 | |||||||
| chr2:26382295 | G | C | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.683-1004G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26382295 | |||||||
| chr2:26382427 | G | T | 1 | a0001c0005t0006g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.683-872G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26382427 | |||||||
| chr2:26382438 | C | T | 1 | a0001c0001t0007g0049 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.683-861C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26382438 | |||||||
| chr2:26382572 | C | CAGA | 282 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(279): Show |
323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.683-723_683-721dup others(3): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 26382572 | ||||||
| chr2:26382647 | T | G | 1 | a0001c0007t0026g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.683-652T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26382647 | |||||||
| chr2:26382824 | A | T | 2 | a0001c0001t0006g0005 a0001c0001t0006g0104 |
5 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-475A>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26382824 | |||||||
| chr2:26383286 | T | C | 66 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(63): Show |
75 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.683-13T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 6/9 | chr2 | 26383286 | |||||||
| chr2:26383466 | A | G | 8 | a0001c0001t0003g0062 a0001c0001t0003g0075 a0001c0001t0009g0067 others(5): Show |
8 | HG01943.hp2 NA18944.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.731+119A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26383466 | |||||||
| chr2:26383479 | T | A | 67 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(64): Show |
72 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.731+132T>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26383479 | |||||||
| chr2:26383534 | C | A | 1 | a0001c0002t0001g0118 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.731+187C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26383534 | |||||||
| chr2:26383597 | G | A | 39 | a0001c0001t0005g0022 a0001c0001t0005g0252 a0001c0001t0005g0253 others(36): Show |
40 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.731+250G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26383597 | |||||||
| chr2:26383605 | G | A | 2 | a0001c0003t0004g0152 a0001c0003t0004g0153 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.731+258G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26383605 | |||||||
| chr2:26383816 | G | A | 1 | a0001c0002t0001g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.731+469G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26383816 | |||||||
| chr2:26383913 | T | C | 1 | a0001c0007t0026g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.731+566T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26383913 | |||||||
| chr2:26383953 | T | G | 58 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0011 others(55): Show |
63 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.731+606T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26383953 | |||||||
| chr2:26384111 | C | T | 2 | a0001c0001t0005g0253 a0001c0001t0005g0267 |
2 | HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.731+764C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26384111 | |||||||
| chr2:26384126 | C | A | 1 | a0001c0001t0003g0077 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.731+779C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26384126 | |||||||
| chr2:26384174 | C | A | 13 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(10): Show |
16 | HG00408.hp1 HG00609.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.732-785C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26384174 | |||||||
| chr2:26384348 | A | C | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.732-611A>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26384348 | |||||||
| chr2:26384404 | G | A | 1 | a0001c0001t0002g0193 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.732-555G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26384404 | |||||||
| chr2:26384675 | A | G | 5 | a0001c0001t0003g0066 a0001c0001t0003g0071 a0001c0001t0003g0072 others(2): Show |
5 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.732-284A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26384675 | |||||||
| chr2:26384758 | C | G | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.732-201C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26384758 | |||||||
| chr2:26384855 | A | C | 1 | a0001c0001t0003g0087 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.732-104A>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26384855 | |||||||
| chr2:26384947 | T | C | 66 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(63): Show |
75 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.732-12T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 7/9 | chr2 | 26384947 | |||||||
| chr2:26385194 | T | C | 1 | a0001c0001t0005g0284 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.912+55T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 8/9 | chr2 | 26385194 | |||||||
| chr2:26385396 | G | A | 1 | a0001c0006t0006g0027 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.912+257G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 8/9 | chr2 | 26385396 | |||||||
| chr2:26385434 | A | G | 2 | a0001c0001t0003g0053 a0001c0001t0003g0054 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.912+295A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 8/9 | chr2 | 26385434 | |||||||
| chr2:26385782 | C | T | 1 | a0001c0002t0001g0154 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.913-572C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 8/9 | chr2 | 26385782 | |||||||
| chr2:26385783 | G | A | 64 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(61): Show |
73 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.913-571G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 8/9 | chr2 | 26385783 | |||||||
| chr2:26385783 | G | T | 1 | a0001c0001t0002g0237 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.913-571G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 8/9 | chr2 | 26385783 | |||||||
| chr2:26385846 | T | G | 24 | a0001c0001t0024g0213 a0001c0003t0004g0008 a0001c0003t0004g0033 others(21): Show |
26 | HG00558.hp2 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.913-508T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 8/9 | chr2 | 26385846 | |||||||
| chr2:26385980 | A | G | 1 | a0001c0001t0008g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.913-374A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 8/9 | chr2 | 26385980 | |||||||
| chr2:26386045 | G | A | 13 | a0001c0001t0007g0003 a0001c0001t0007g0040 a0001c0001t0007g0041 others(10): Show |
16 | HG00408.hp1 HG00609.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.913-309G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 8/9 | chr2 | 26386045 | |||||||
| chr2:26386091 | G | C | 1 | a0001c0001t0002g0186 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.913-263G>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 8/9 | chr2 | 26386091 | |||||||
| chr2:26386144 | G | T | 2 | a0001c0002t0001g0132 a0001c0002t0001g0138 |
2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.913-210G>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 8/9 | chr2 | 26386144 | |||||||
| chr2:26386336 | T | G | 9 | a0001c0001t0008g0028 a0001c0001t0008g0029 a0001c0001t0008g0030 others(6): Show |
9 | HG00741.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.913-18T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 8/9 | chr2 | 26386336 | |||||||
| chr2:26386601 | G | A | 56 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(53): Show |
74 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.1095+65G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | chr2 | 26386601 | |||||||
| chr2:26386662 | G | A | 1 | a0001c0001t0003g0090 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1095+126G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | chr2 | 26386662 | |||||||
| chr2:26386922 | G | A | 5 | a0001c0004t0004g0107 a0001c0004t0004g0119 a0001c0004t0004g0139 others(2): Show |
5 | HG00558.hp2 NA18942.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+386G>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | chr2 | 26386922 | |||||||
| chr2:26387083 | A | T | 1 | a0001c0001t0034g0174 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1095+547A>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | chr2 | 26387083 | |||||||
| chr2:26387193 | A | G | 5 | a0001c0001t0003g0057 a0001c0001t0003g0088 a0001c0001t0003g0096 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+657A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | chr2 | 26387193 | |||||||
| chr2:26387488 | C | T | 1 | a0001c0001t0002g0190 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1095+952C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | chr2 | 26387488 | |||||||
| chr2:26387536 | C | CA | 65 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(62): Show |
74 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1095+1010dupA | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 26387536 | ||||||
| chr2:26387695 | CAA | C | 251 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(248): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1095+1176_1095+117 others(6): Show |
SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 26387695 | ||||||
| chr2:26387912 | C | A | 2 | a0001c0001t0003g0060 a0001c0001t0003g0089 |
2 | HG01168.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1096-1093C>A | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | chr2 | 26387912 | |||||||
| chr2:26388158 | A | G | 1 | a0001c0003t0011g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1096-847A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | chr2 | 26388158 | |||||||
| chr2:26388166 | C | G | 168 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(165): Show |
188 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1096-839C>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | chr2 | 26388166 | |||||||
| chr2:26388251 | A | G | 1 | a0001c0007t0026g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1096-754A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | chr2 | 26388251 | |||||||
| chr2:26388267 | A | G | 2 | a0001c0001t0006g0005 a0001c0001t0006g0104 |
5 | HG02486.hp1 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-738A>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | chr2 | 26388267 | |||||||
| chr2:26388472 | C | T | 1 | a0001c0001t0005g0262 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1096-533C>T | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | chr2 | 26388472 | |||||||
| chr2:26388502 | T | G | 4 | a0001c0002t0001g0113 a0001c0002t0001g0124 a0001c0002t0001g0125 others(1): Show |
4 | HG01981.hp2 HG02004.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-503T>G | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | chr2 | 26388502 | |||||||
| chr2:26388799 | T | C | 255 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0017 others(252): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1096-206T>C | SELENOI | ENSG00000138018.19 | transcript | ENST00000260585.12 | protein_coding | 9/9 | chr2 | 26388799 |