Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51714 |
| ensemblid | ENSG00000198843.14 |
| hgncid | 18136 |
| symbol | SELENOT |
| name | selenoprotein T |
| refseq_nuc | NM_016275.5 |
| refseq_prot | NP_057359.2 |
| ensembl_nuc | ENST00000471696.6 |
| ensembl_prot | ENSP00000418910.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 150603321 |
| end | 150630436 |
| strand | + |
| ver | v1.2 |
| region | chr3:150603321-150630436 |
| region5000 | chr3:150598321-150635436 |
| regionname0 | SELENOT_chr3_150603321_150630436 |
| regionname5000 | SELENOT_chr3_150598321_150635436 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 585 | 376 | 90 | 76 | 156 | 12 | 40 | SELENOT_chr3_150598321_150635436 | SELENOT | ATGAG others(580): Show |
chr3 | 150598321 | 150635436 | ||
| a0001c0002 | 0/0 | 585 | 4 | 4 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | ATGAG others(580): Show |
chr3 | 150598321 | 150635436 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3437 | 135 | 7 | 26 | 81 | 4 | 16 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0002 | 0/0 | 3437 | 116 | 21 | 19 | 64 | 3 | 9 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0003 | 1/0 | 3437 | 47 | 23 | 17 | 0 | 2 | 4 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0004 | 0/0 | 3437 | 28 | 7 | 10 | 4 | 1 | 6 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0005 | 0/0 | 3437 | 6 | 4 | 2 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0006 | 0/0 | 3437 | 5 | 5 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0007 | 0/0 | 3437 | 5 | 5 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0008 | 0/0 | 3437 | 4 | 4 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0009 | 0/0 | 3437 | 4 | 4 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0010 | 0/0 | 3437 | 3 | 0 | 2 | 0 | 1 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0011 | 0/0 | 3437 | 3 | 3 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0012 | 0/0 | 3437 | 3 | 3 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0013 | 0/0 | 3437 | 2 | 0 | 0 | 0 | 0 | 2 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0014 | 0/0 | 3437 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0015 | 0/0 | 3437 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0016 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0017 | 0/0 | 3437 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0018 | 0/0 | 3469 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3464): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0019 | 0/0 | 3437 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0020 | 0/0 | 3437 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0021 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0022 | 0/0 | 3437 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0023 | 0/0 | 3437 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0024 | 0/0 | 3437 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0025 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0026 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0001t0027 | 0/0 | 3437 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| a0001c0002t0002 | 0/0 | 3437 | 4 | 4 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | GCAGT others(3432): Show |
chr3 | 150598321 | 150635436 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 28 | 0 | 9 | 18 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0004 | 0/0 | 7 | 4 | 1 | 0 | 0 | 2 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0002 | 0/0 | 13 | 1 | 1 | 9 | 0 | 2 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0005 | 0/0 | 7 | 2 | 2 | 3 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0008 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0009 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0023 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0048 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0003 | 1/0 | 6 | 1 | 2 | 0 | 1 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0016 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0024 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0007 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0005g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0007g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0008g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0009g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0010g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0010g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0011g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0011g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0012g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0013g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0013g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0014g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0015g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0016g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0017g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0018g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0019g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0020g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0021g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0022g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0023g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0024g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0025g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0026g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0001t0027g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0002t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0024 | EUR | FIN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0148 | EUR | FIN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00323 | hp2 | a0001 | c0001 | t0027 | g0093 | EUR | FIN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00438 | hp1 | a0001 | c0001 | t0022 | g0009 | EAS | CHS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00621 | hp2 | a0001 | c0001 | t0014 | g0001 | EAS | CHS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | CHS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0144 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01069 | hp1 | a0001 | c0001 | t0010 | g0001 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01074 | hp1 | a0001 | c0001 | t0010 | g0006 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0139 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0236 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0034 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0051 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0044 | EUR | IBS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0042 | EUR | IBS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0222 | EUR | IBS | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0141 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02071 | hp1 | a0001 | c0001 | t0014 | g0031 | EAS | KHV | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | KHV | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0152 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0142 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | CDX | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0176 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0027 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02280 | hp1 | a0001 | c0001 | t0016 | g0071 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PEL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0050 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0069 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0137 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0045 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0135 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02630 | hp2 | a0001 | c0001 | t0025 | g0234 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0003 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02738 | hp2 | a0001 | c0001 | t0019 | g0126 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0050 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02818 | hp1 | a0001 | c0001 | t0012 | g0003 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0237 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0235 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0132 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0131 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0134 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03098 | hp1 | a0001 | c0001 | t0021 | g0233 | AFR | MSL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | MSL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0033 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0232 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | MSL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | MSL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | MSL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | MSL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0129 | AFR | MSL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | MSL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0070 | AFR | ESN | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0238 | AFR | MSL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0226 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0240 | SAS | STU | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | STU | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03704 | hp1 | a0001 | c0001 | t0013 | g0032 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03710 | hp2 | a0001 | c0001 | t0024 | g0009 | SAS | PJL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0224 | SAS | BEB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03942 | hp2 | a0001 | c0001 | t0013 | g0096 | SAS | BEB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | STU | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0227 | SAS | BEB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0136 | SAS | STU | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | YRI | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | CHB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18906 | hp1 | a0001 | c0001 | t0012 | g0003 | AFR | YRI | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | YRI | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18949 | hp1 | a0001 | c0001 | t0015 | g0157 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18949 | hp2 | a0001 | c0001 | t0023 | g0014 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18992 | hp2 | a0001 | c0001 | t0020 | g0105 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18999 | hp1 | a0001 | c0001 | t0017 | g0128 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | LWK | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | LWK | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0027 | AFR | LWK | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | LWK | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0045 | AFR | YRI | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | YRI | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ASW | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ASW | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0001 | EUR | TSI | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | GIH | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| NA20905 | hp2 | a0001 | c0001 | t0018 | g0116 | SAS | GIH | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0140 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02109 | hp1 | a0001 | c0001 | t0026 | g0022 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0143 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0166 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0130 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | MSL | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | USA | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0033 | AFR | USA | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0082 | REF | REF | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0003 | REF | REF | SELENOT_chr3_150598321_150635436 | SELENOT | chr3 | 150598321 | 150635436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:150622388 | T | A | 1 | a0001c0002 | 4 | HG02257.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
synonymous_variant | LOW | c.141T>A | p.Val47Val | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 2/6 | 183/3437 | 141/588 | 47/195 | chr3 | 150622388 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:150603336 | G | A | 1 | a0001c0001t0010 | 3 | HG01069.hp1 HG01074.hp1 NA20752.hp1 |
5_prime_UTR_variant | MODIFIER | c.-27G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/6 | 27 | chr3 | 150603336 | ||||||
| chr3:150627137 | C | T | 1 | a0001c0001t0027 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 5/6 | 3 | chr3 | 150627137 | ||||||
| chr3:150627158 | T | C | 1 | a0001c0001t0015 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*24T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 5/6 | 24 | chr3 | 150627158 | ||||||
| chr3:150627802 | G | C | 1 | a0001c0001t0016 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*173G>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 668 | chr3 | 150627802 | ||||||
| chr3:150627877 | A | G | 1 | a0001c0001t0004 | 28 | HG00323.hp1 HG00735.hp1 HG01071.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*248A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 743 | chr3 | 150627877 | ||||||
| chr3:150627903 | T | G | 12 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(9): Show |
160 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*274T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 769 | chr3 | 150627903 | ||||||
| chr3:150628143 | A | G | 2 | a0001c0001t0006 a0001c0001t0007 |
10 | HG02109.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*514A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 1009 | chr3 | 150628143 | ||||||
| chr3:150628187 | T | C | 2 | a0001c0001t0005 a0001c0001t0021 |
7 | HG01433.hp2 HG01496.hp2 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*558T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 1053 | chr3 | 150628187 | ||||||
| chr3:150628280 | T | C | 1 | a0001c0001t0013 | 2 | HG03704.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*651T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 1146 | chr3 | 150628280 | ||||||
| chr3:150628350 | C | T | 1 | a0001c0001t0026 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*721C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 1216 | chr3 | 150628350 | ||||||
| chr3:150628392 | T | G | 1 | a0001c0001t0006 | 5 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*763T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 1258 | chr3 | 150628392 | ||||||
| chr3:150628580 | A | G | 1 | a0001c0001t0008 | 4 | HG02258.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*951A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 1446 | chr3 | 150628580 | ||||||
| chr3:150628626 | A | G | 1 | a0001c0001t0020 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*997A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 1492 | chr3 | 150628626 | ||||||
| chr3:150628673 | T | G | 1 | a0001c0001t0011 | 3 | HG02145.hp2 HG02615.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1044T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 1539 | chr3 | 150628673 | ||||||
| chr3:150628684 | T | C | 13 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(10): Show |
171 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*1055T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 1550 | chr3 | 150628684 | ||||||
| chr3:150628785 | A | G | 2 | a0001c0001t0006 a0001c0001t0007 |
10 | HG02109.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1156A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 1651 | chr3 | 150628785 | ||||||
| chr3:150628867 | A | G | 9 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0013 others(6): Show |
146 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*1238A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 1733 | chr3 | 150628867 | ||||||
| chr3:150629041 | G | A | 1 | a0001c0001t0017 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1412G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 1907 | chr3 | 150629041 | ||||||
| chr3:150629144 | T | TGTTGAAT others(25): Show |
1 | a0001c0001t0018 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1516_*1547dupGTTG others(28): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 2043 | INFO_REALIGN_3_PRIME | chr3 | 150629144 | |||||
| chr3:150629192 | G | A | 1 | a0001c0001t0014 | 2 | HG00621.hp2 HG02071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1563G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 2058 | chr3 | 150629192 | ||||||
| chr3:150629396 | T | G | 2 | a0001c0001t0009 a0001c0001t0025 |
5 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1767T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 2262 | chr3 | 150629396 | ||||||
| chr3:150629523 | C | A | 1 | a0001c0001t0016 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1894C>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 2389 | chr3 | 150629523 | ||||||
| chr3:150629600 | A | T | 1 | a0001c0001t0024 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1971A>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 2466 | chr3 | 150629600 | ||||||
| chr3:150629703 | C | T | 2 | a0001c0001t0009 a0001c0001t0025 |
5 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2074C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 2569 | chr3 | 150629703 | ||||||
| chr3:150630019 | A | C | 1 | a0001c0001t0025 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2390A>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 2885 | chr3 | 150630019 | ||||||
| chr3:150630046 | G | A | 10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(7): Show |
157 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2417G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 2912 | chr3 | 150630046 | ||||||
| chr3:150630113 | A | G | 1 | a0001c0001t0012 | 3 | HG02717.hp1 HG02818.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2484A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 2979 | chr3 | 150630113 | ||||||
| chr3:150630245 | G | A | 1 | a0001c0001t0016 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2616G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 3111 | chr3 | 150630245 | ||||||
| chr3:150630295 | G | T | 1 | a0001c0001t0023 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2666G>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 3161 | chr3 | 150630295 | ||||||
| chr3:150630341 | T | A | 3 | a0001c0001t0018 a0001c0001t0019 a0001c0001t0022 |
3 | HG00438.hp1 HG02738.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2712T>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 3207 | chr3 | 150630341 | ||||||
| chr3:150630342 | A | T | 1 | a0001c0001t0021 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2713A>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 6/6 | 3208 | chr3 | 150630342 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:150603724 | T | C | 1 | a0001c0001t0002g0052 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.137+225T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150603724 | |||||||
| chr3:150603751 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
8 | HG01433.hp1 HG01981.hp2 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.137+252G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150603751 | |||||||
| chr3:150603798 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.137+299G>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150603798 | |||||||
| chr3:150603836 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.137+337G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150603836 | |||||||
| chr3:150603896 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.137+397G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150603896 | |||||||
| chr3:150604218 | A | G | 1 | a0001c0001t0004g0240 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.137+719A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150604218 | |||||||
| chr3:150604382 | A | T | 1 | a0001c0001t0001g0239 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.137+883A>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150604382 | |||||||
| chr3:150604453 | C | T | 19 | a0001c0001t0003g0024 a0001c0001t0003g0058 a0001c0001t0003g0224 others(16): Show |
23 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.137+954C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150604453 | |||||||
| chr3:150604611 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.137+1112C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150604611 | |||||||
| chr3:150604631 | C | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(232): Show |
351 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.137+1132C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150604631 | |||||||
| chr3:150604889 | T | G | 5 | a0001c0001t0003g0058 a0001c0001t0003g0224 a0001c0001t0003g0225 others(2): Show |
5 | HG01175.hp2 HG02300.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+1390T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150604889 | |||||||
| chr3:150605037 | C | CA | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(123): Show |
198 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.137+1555dupA | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150605037 | ||||||
| chr3:150605037 | C | CAAAA | 15 | a0001c0001t0003g0024 a0001c0001t0003g0058 a0001c0001t0003g0224 others(12): Show |
18 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.137+1552_137+1555d others(6): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150605037 | ||||||
| chr3:150605207 | A | T | 1 | a0001c0001t0001g0239 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.137+1708A>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150605207 | |||||||
| chr3:150605280 | C | G | 1 | a0001c0001t0005g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.137+1781C>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150605280 | |||||||
| chr3:150605456 | AAGTAGTA others(85): Show |
A | 1 | a0001c0001t0001g0037 | 2 | HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.137+1961_137+2052d others(94): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150605456 | ||||||
| chr3:150605545 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.137+2046T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150605545 | |||||||
| chr3:150605596 | T | A | 1 | a0001c0001t0003g0015 | 3 | HG02647.hp2 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.137+2097T>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150605596 | |||||||
| chr3:150605638 | A | AT | 91 | a0001c0001t0001g0055 a0001c0001t0002g0002 a0001c0001t0002g0005 others(88): Show |
129 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.137+2145dupT | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150605638 | ||||||
| chr3:150605834 | A | C | 1 | a0001c0001t0004g0148 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.137+2335A>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150605834 | |||||||
| chr3:150605914 | C | T | 27 | a0001c0001t0004g0007 a0001c0001t0004g0020 a0001c0001t0004g0021 others(24): Show |
38 | HG00323.hp1 HG00735.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.137+2415C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150605914 | |||||||
| chr3:150605955 | C | T | 1 | a0001c0001t0017g0128 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.137+2456C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150605955 | |||||||
| chr3:150606040 | T | G | 3 | a0001c0001t0008g0027 a0001c0001t0008g0069 a0001c0001t0008g0070 |
4 | HG02258.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+2541T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150606040 | |||||||
| chr3:150606125 | G | GT | 93 | a0001c0001t0001g0055 a0001c0001t0001g0127 a0001c0001t0002g0002 others(90): Show |
134 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.137+2637dupT | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150606125 | ||||||
| chr3:150606150 | C | CT | 8 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0127 others(5): Show |
11 | HG01981.hp2 HG02630.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.137+2666dupT | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150606150 | ||||||
| chr3:150606150 | CT | C | 115 | a0001c0001t0001g0055 a0001c0001t0002g0002 a0001c0001t0002g0005 others(112): Show |
164 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.137+2666delT | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150606150 | ||||||
| chr3:150606289 | C | T | 3 | a0001c0001t0008g0027 a0001c0001t0008g0069 a0001c0001t0008g0070 |
4 | HG02258.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+2790C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150606289 | |||||||
| chr3:150606433 | A | G | 3 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0002g0171 |
3 | NA18974.hp1 NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.137+2934A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150606433 | |||||||
| chr3:150606476 | T | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0228 a0001c0001t0003g0229 others(2): Show |
7 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.137+2977T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150606476 | |||||||
| chr3:150606535 | T | C | 27 | a0001c0001t0004g0007 a0001c0001t0004g0020 a0001c0001t0004g0021 others(24): Show |
38 | HG00323.hp1 HG00735.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.137+3036T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150606535 | |||||||
| chr3:150606559 | CTT | C | 90 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(87): Show |
128 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.137+3061_137+3062d others(4): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150606559 | |||||||
| chr3:150606666 | C | T | 11 | a0001c0001t0003g0058 a0001c0001t0003g0224 a0001c0001t0003g0225 others(8): Show |
12 | HG01175.hp2 HG01433.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.137+3167C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150606666 | |||||||
| chr3:150606707 | C | G | 1 | a0001c0001t0004g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.137+3208C>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150606707 | |||||||
| chr3:150606707 | C | T | 1 | a0001c0001t0003g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.137+3208C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150606707 | |||||||
| chr3:150606849 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.137+3350G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150606849 | |||||||
| chr3:150606897 | A | G | 1 | a0001c0001t0007g0143 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.137+3398A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150606897 | |||||||
| chr3:150607165 | T | A | 1 | a0001c0001t0001g0239 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.137+3666T>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150607165 | |||||||
| chr3:150607221 | T | A | 1 | a0001c0001t0001g0239 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.137+3722T>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150607221 | |||||||
| chr3:150607324 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0001g0125 |
5 | NA18946.hp2 NA18975.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+3825A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150607324 | |||||||
| chr3:150607345 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.137+3846T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150607345 | |||||||
| chr3:150607406 | C | T | 4 | a0001c0001t0003g0040 a0001c0001t0003g0163 a0001c0001t0003g0164 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+3907C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150607406 | |||||||
| chr3:150607416 | G | A | 1 | a0001c0001t0004g0145 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+3917G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150607416 | |||||||
| chr3:150607640 | G | C | 1 | a0001c0001t0007g0129 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.137+4141G>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150607640 | |||||||
| chr3:150607642 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0072 |
3 | HG01952.hp1 HG02004.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.137+4143G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150607642 | |||||||
| chr3:150607711 | G | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(83): Show |
146 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.137+4212G>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150607711 | |||||||
| chr3:150607875 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(215): Show |
329 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(326): Show |
intron_variant | MODIFIER | c.137+4376T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150607875 | |||||||
| chr3:150607930 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.137+4431G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150607930 | |||||||
| chr3:150608046 | G | C | 1 | a0001c0001t0001g0074 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.137+4547G>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150608046 | |||||||
| chr3:150608062 | G | A | 1 | a0001c0001t0003g0160 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.137+4563G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150608062 | |||||||
| chr3:150608421 | A | G | 4 | a0001c0001t0009g0050 a0001c0001t0009g0232 a0001c0001t0009g0235 others(1): Show |
5 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+4922A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150608421 | |||||||
| chr3:150608444 | T | G | 1 | a0001c0001t0001g0075 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.137+4945T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150608444 | |||||||
| chr3:150608445 | G | T | 1 | a0001c0001t0001g0075 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.137+4946G>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150608445 | |||||||
| chr3:150608573 | G | C | 1 | a0001c0001t0003g0228 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.137+5074G>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150608573 | |||||||
| chr3:150608748 | G | A | 1 | a0001c0001t0003g0060 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.137+5249G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150608748 | |||||||
| chr3:150608896 | A | G | 1 | a0001c0001t0004g0148 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.137+5397A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150608896 | |||||||
| chr3:150608995 | C | T | 91 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(88): Show |
129 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.137+5496C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150608995 | |||||||
| chr3:150609240 | T | G | 1 | a0001c0001t0007g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.137+5741T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150609240 | |||||||
| chr3:150609494 | C | T | 1 | a0001c0001t0005g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137+5995C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150609494 | |||||||
| chr3:150609495 | G | A | 1 | a0001c0001t0019g0126 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.137+5996G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150609495 | |||||||
| chr3:150609496 | C | T | 13 | a0001c0001t0004g0007 a0001c0001t0004g0020 a0001c0001t0004g0034 others(10): Show |
20 | HG00323.hp1 HG00735.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.137+5997C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150609496 | |||||||
| chr3:150609632 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.137+6133C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150609632 | |||||||
| chr3:150609863 | T | C | 9 | a0001c0001t0006g0131 a0001c0001t0006g0132 a0001c0001t0006g0133 others(6): Show |
10 | HG02109.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+6364T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150609863 | |||||||
| chr3:150609927 | A | T | 1 | a0001c0001t0002g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.137+6428A>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150609927 | |||||||
| chr3:150610053 | A | G | 4 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(1): Show |
4 | HG00741.hp1 HG02683.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+6554A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150610053 | |||||||
| chr3:150610073 | A | G | 1 | a0001c0001t0004g0020 | 3 | NA18951.hp2 NA18984.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.137+6574A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150610073 | |||||||
| chr3:150610209 | C | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(220): Show |
337 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.137+6710C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150610209 | |||||||
| chr3:150610229 | A | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(204): Show |
317 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.137+6730A>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150610229 | |||||||
| chr3:150610236 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.137+6737A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150610236 | |||||||
| chr3:150610449 | A | G | 3 | a0001c0001t0008g0027 a0001c0001t0008g0069 a0001c0001t0008g0070 |
4 | HG02258.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+6950A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150610449 | |||||||
| chr3:150610662 | G | T | 1 | a0001c0001t0006g0135 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.137+7163G>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150610662 | |||||||
| chr3:150610714 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.137+7215A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150610714 | |||||||
| chr3:150610832 | T | TACTC | 6 | a0001c0001t0005g0051 a0001c0001t0005g0166 a0001c0001t0005g0236 others(3): Show |
7 | HG01433.hp2 HG01496.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.137+7334_137+7337d others(6): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150610832 | ||||||
| chr3:150610916 | C | G | 1 | a0001c0001t0002g0217 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.137+7417C>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150610916 | |||||||
| chr3:150611004 | C | CGT | 36 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
49 | HG00408.hp2 HG00609.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.137+7536_137+7537d others(4): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150611004 | ||||||
| chr3:150611004 | C | CGTGT | 25 | a0001c0001t0001g0117 a0001c0001t0002g0022 a0001c0001t0002g0042 others(22): Show |
36 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.137+7534_137+7537d others(6): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150611004 | ||||||
| chr3:150611004 | C | CGTGTGT | 24 | a0001c0001t0002g0008 a0001c0001t0002g0043 a0001c0001t0002g0044 others(21): Show |
33 | HG01192.hp2 HG01255.hp2 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.137+7532_137+7537d others(8): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150611004 | ||||||
| chr3:150611004 | C | CGTGTGTG others(1): Show |
11 | a0001c0001t0002g0005 a0001c0001t0002g0036 a0001c0001t0002g0047 others(8): Show |
19 | HG00609.hp1 HG01099.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.137+7530_137+7537d others(10): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150611004 | ||||||
| chr3:150611004 | C | CGTGTGTG others(3): Show |
32 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0048 others(29): Show |
48 | HG00423.hp1 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.137+7528_137+7537d others(12): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150611004 | ||||||
| chr3:150611004 | C | CGTGTGTG others(5): Show |
9 | a0001c0001t0002g0023 a0001c0001t0002g0158 a0001c0001t0002g0204 others(6): Show |
11 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.137+7526_137+7537d others(14): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150611004 | ||||||
| chr3:150611004 | C | CGTGTGTG others(7): Show |
5 | a0001c0001t0002g0009 a0001c0001t0002g0211 a0001c0001t0002g0212 others(2): Show |
7 | HG00438.hp1 HG00673.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.137+7524_137+7537d others(16): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150611004 | ||||||
| chr3:150611004 | C | CGTGTGTG others(9): Show |
3 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 |
3 | HG02080.hp1 HG02132.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.137+7522_137+7537d others(18): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150611004 | ||||||
| chr3:150611004 | C | CGTGTGTG others(11): Show |
1 | a0001c0001t0002g0216 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.137+7520_137+7537d others(20): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150611004 | ||||||
| chr3:150611004 | CGT | C | 5 | a0001c0001t0001g0077 a0001c0001t0005g0051 a0001c0001t0005g0236 others(2): Show |
6 | HG01433.hp2 HG01496.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+7536_137+7537d others(4): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150611004 | ||||||
| chr3:150611004 | CGTGTGT | C | 2 | a0001c0001t0001g0076 a0001c0001t0003g0039 |
3 | HG02922.hp1 HG03139.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.137+7532_137+7537d others(8): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150611004 | ||||||
| chr3:150611037 | A | G | 2 | a0001c0001t0002g0170 a0001c0001t0002g0171 |
2 | NA18974.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.137+7538A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150611037 | |||||||
| chr3:150611039 | T | G | 2 | a0001c0001t0002g0170 a0001c0001t0002g0171 |
2 | NA18974.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.137+7540T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150611039 | |||||||
| chr3:150611276 | C | G | 91 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(88): Show |
129 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.137+7777C>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150611276 | |||||||
| chr3:150611325 | ATATGT | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(83): Show |
146 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.137+7829_137+7833d others(7): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150611325 | ||||||
| chr3:150611355 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.137+7856A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150611355 | |||||||
| chr3:150611458 | A | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(204): Show |
317 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.137+7959A>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150611458 | |||||||
| chr3:150611591 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.137+8092T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150611591 | |||||||
| chr3:150611698 | C | T | 90 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(87): Show |
128 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.137+8199C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150611698 | |||||||
| chr3:150611756 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.137+8257C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150611756 | |||||||
| chr3:150611838 | G | A | 1 | a0001c0001t0003g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.137+8339G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150611838 | |||||||
| chr3:150611890 | C | CG | 28 | a0001c0001t0001g0029 a0001c0001t0001g0053 a0001c0001t0001g0078 others(25): Show |
29 | HG00438.hp2 HG00673.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.137+8395dupG | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150611890 | ||||||
| chr3:150611893 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.137+8394G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150611893 | |||||||
| chr3:150611894 | G | A | 13 | a0001c0001t0004g0007 a0001c0001t0004g0020 a0001c0001t0004g0034 others(10): Show |
20 | HG00323.hp1 HG00735.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.137+8395G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150611894 | |||||||
| chr3:150611896 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.137+8397A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150611896 | |||||||
| chr3:150611929 | C | T | 5 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0003g0162 others(2): Show |
5 | HG02630.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+8430C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150611929 | |||||||
| chr3:150612659 | A | G | 9 | a0001c0001t0006g0131 a0001c0001t0006g0132 a0001c0001t0006g0133 others(6): Show |
10 | HG02109.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+9160A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150612659 | |||||||
| chr3:150612812 | C | T | 1 | a0001c0001t0005g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137+9313C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150612812 | |||||||
| chr3:150612849 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.137+9350T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150612849 | |||||||
| chr3:150612912 | A | G | 3 | a0001c0001t0003g0016 a0001c0001t0003g0026 a0001c0001t0003g0066 |
6 | HG00639.hp1 HG00642.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+9413A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150612912 | |||||||
| chr3:150612948 | A | G | 1 | a0001c0001t0003g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.138-9437A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150612948 | |||||||
| chr3:150613234 | A | G | 1 | a0001c0001t0005g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.138-9151A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150613234 | |||||||
| chr3:150613486 | T | C | 5 | a0001c0001t0003g0058 a0001c0001t0003g0224 a0001c0001t0003g0225 others(2): Show |
5 | HG01175.hp2 HG02300.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-8899T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150613486 | |||||||
| chr3:150613526 | A | G | 1 | a0001c0001t0002g0215 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.138-8859A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150613526 | |||||||
| chr3:150613665 | C | CT | 31 | a0001c0001t0001g0018 a0001c0001t0001g0075 a0001c0001t0001g0079 others(28): Show |
37 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.138-8692dupT | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150613665 | ||||||
| chr3:150613665 | C | CTT | 80 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(77): Show |
129 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.138-8693_138-8692d others(4): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150613665 | ||||||
| chr3:150613665 | C | CTTT | 26 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0099 others(23): Show |
29 | HG00408.hp2 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.138-8694_138-8692d others(5): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150613665 | ||||||
| chr3:150613665 | CT | C | 15 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0072 others(12): Show |
21 | HG01167.hp1 HG01256.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.138-8692delT | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150613665 | ||||||
| chr3:150613665 | CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0002g0036 a0001c0001t0002g0154 a0001c0001t0002g0155 |
4 | HG02145.hp1 HG02451.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-8705_138-8692d others(16): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150613665 | ||||||
| chr3:150613801 | T | C | 90 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(87): Show |
128 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.138-8584T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150613801 | |||||||
| chr3:150613856 | C | T | 11 | a0001c0001t0003g0058 a0001c0001t0003g0224 a0001c0001t0003g0225 others(8): Show |
12 | HG01175.hp2 HG01433.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.138-8529C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150613856 | |||||||
| chr3:150613948 | CACAGGAG others(9): Show |
C | 5 | a0001c0001t0003g0058 a0001c0001t0003g0224 a0001c0001t0003g0225 others(2): Show |
5 | HG01175.hp2 HG02300.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-8436_138-8421d others(18): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150613948 | |||||||
| chr3:150614021 | A | T | 1 | a0001c0001t0002g0185 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.138-8364A>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150614021 | |||||||
| chr3:150614022 | A | T | 1 | a0001c0001t0002g0185 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.138-8363A>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150614022 | |||||||
| chr3:150614023 | T | TTTTTTTT others(4604): Show |
1 | a0001c0001t0002g0185 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.138-8362_138-8361i others(4613): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150614023 | |||||||
| chr3:150614224 | G | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(55): Show |
103 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.138-8161G>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150614224 | |||||||
| chr3:150614343 | T | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(82): Show |
121 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.138-8042T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150614343 | |||||||
| chr3:150614408 | T | TG | 4 | a0001c0001t0002g0194 a0001c0001t0007g0143 a0001c0001t0013g0096 others(1): Show |
4 | HG01346.hp1 HG02109.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-7974dupG | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150614408 | ||||||
| chr3:150614412 | T | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(195): Show |
308 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.138-7973T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150614412 | |||||||
| chr3:150614413 | T | G | 2 | a0001c0001t0001g0239 a0001c0001t0008g0069 |
2 | HG02572.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.138-7972T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150614413 | |||||||
| chr3:150614474 | A | C | 5 | a0001c0001t0003g0058 a0001c0001t0003g0224 a0001c0001t0003g0225 others(2): Show |
5 | HG01175.hp2 HG02300.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-7911A>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150614474 | |||||||
| chr3:150614511 | G | A | 1 | a0001c0001t0002g0208 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.138-7874G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150614511 | |||||||
| chr3:150614678 | A | G | 4 | a0001c0001t0005g0051 a0001c0001t0005g0236 a0001c0001t0005g0237 others(1): Show |
5 | HG01433.hp2 HG01496.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-7707A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150614678 | |||||||
| chr3:150614772 | T | C | 4 | a0001c0001t0009g0050 a0001c0001t0009g0232 a0001c0001t0009g0235 others(1): Show |
5 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-7613T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150614772 | |||||||
| chr3:150614869 | T | A | 5 | a0001c0001t0003g0058 a0001c0001t0003g0224 a0001c0001t0003g0225 others(2): Show |
5 | HG01175.hp2 HG02300.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-7516T>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150614869 | |||||||
| chr3:150614931 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.138-7454C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150614931 | |||||||
| chr3:150615069 | T | A | 87 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(84): Show |
124 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.138-7316T>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150615069 | |||||||
| chr3:150615135 | A | G | 5 | a0001c0001t0003g0024 a0001c0001t0003g0228 a0001c0001t0003g0229 others(2): Show |
7 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-7250A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150615135 | |||||||
| chr3:150615194 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(205): Show |
320 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.138-7191T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150615194 | |||||||
| chr3:150615318 | A | G | 1 | a0001c0001t0005g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.138-7067A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150615318 | |||||||
| chr3:150615547 | C | T | 1 | a0001c0001t0016g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-6838C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150615547 | |||||||
| chr3:150615754 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.138-6631C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150615754 | |||||||
| chr3:150615890 | A | G | 4 | a0001c0001t0002g0044 a0001c0001t0002g0049 a0001c0001t0002g0194 others(1): Show |
6 | HG01069.hp2 HG01071.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.138-6495A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150615890 | |||||||
| chr3:150615905 | CA | C | 3 | a0001c0001t0008g0027 a0001c0001t0008g0069 a0001c0001t0008g0070 |
4 | HG02258.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-6476delA | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150615905 | ||||||
| chr3:150615924 | G | A | 3 | a0001c0001t0008g0027 a0001c0001t0008g0069 a0001c0001t0008g0070 |
4 | HG02258.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-6461G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150615924 | |||||||
| chr3:150615951 | A | G | 1 | a0001c0001t0004g0140 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.138-6434A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150615951 | |||||||
| chr3:150615965 | G | T | 1 | a0001c0001t0007g0143 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.138-6420G>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150615965 | |||||||
| chr3:150616205 | T | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0083 |
2 | NA18995.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.138-6180T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150616205 | |||||||
| chr3:150616330 | A | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(82): Show |
121 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.138-6055A>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150616330 | |||||||
| chr3:150616375 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.138-6010C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150616375 | |||||||
| chr3:150616437 | T | G | 2 | a0001c0001t0003g0040 a0001c0001t0003g0164 |
3 | HG01167.hp2 HG01169.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.138-5948T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150616437 | |||||||
| chr3:150616438 | C | T | 2 | a0001c0001t0003g0040 a0001c0001t0003g0164 |
3 | HG01167.hp2 HG01169.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.138-5947C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150616438 | |||||||
| chr3:150616439 | A | G | 2 | a0001c0001t0003g0040 a0001c0001t0003g0164 |
3 | HG01167.hp2 HG01169.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.138-5946A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150616439 | |||||||
| chr3:150616444 | C | T | 2 | a0001c0001t0003g0040 a0001c0001t0003g0164 |
3 | HG01167.hp2 HG01169.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.138-5941C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150616444 | |||||||
| chr3:150616508 | AAAAC | A | 9 | a0001c0001t0003g0025 a0001c0001t0003g0064 a0001c0001t0003g0065 others(6): Show |
13 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.138-5870_138-5867d others(6): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150616508 | ||||||
| chr3:150616644 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0077 a0001c0001t0001g0107 others(2): Show |
8 | HG00621.hp1 HG00738.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.138-5741C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150616644 | |||||||
| chr3:150616721 | G | A | 1 | a0001c0001t0003g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.138-5664G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150616721 | |||||||
| chr3:150616965 | C | T | 4 | a0001c0001t0009g0050 a0001c0001t0009g0232 a0001c0001t0009g0235 others(1): Show |
5 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-5420C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150616965 | |||||||
| chr3:150617075 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0109 |
2 | HG02074.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.138-5310A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150617075 | |||||||
| chr3:150617276 | A | G | 3 | a0001c0001t0008g0027 a0001c0001t0008g0069 a0001c0001t0008g0070 |
4 | HG02258.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-5109A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150617276 | |||||||
| chr3:150617382 | C | T | 1 | a0001c0001t0002g0178 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.138-5003C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150617382 | |||||||
| chr3:150617383 | T | C | 1 | a0001c0001t0005g0166 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.138-5002T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150617383 | |||||||
| chr3:150617524 | C | G | 1 | a0001c0001t0004g0141 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.138-4861C>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150617524 | |||||||
| chr3:150617605 | C | A | 1 | a0001c0001t0016g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-4780C>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150617605 | |||||||
| chr3:150617714 | ATATAATA others(6): Show |
A | 1 | a0001c0001t0001g0239 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.138-4670_138-4658d others(15): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150617714 | |||||||
| chr3:150617744 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(82): Show |
121 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.138-4641A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150617744 | |||||||
| chr3:150617750 | T | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(82): Show |
121 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.138-4635T>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150617750 | |||||||
| chr3:150617783 | C | CA | 121 | a0001c0001t0001g0084 a0001c0001t0002g0002 a0001c0001t0002g0005 others(118): Show |
171 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.138-4593dupA | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150617783 | ||||||
| chr3:150617801 | G | C | 3 | a0001c0001t0008g0027 a0001c0001t0008g0069 a0001c0001t0008g0070 |
4 | HG02258.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-4584G>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150617801 | |||||||
| chr3:150617838 | T | TGTTTGGT others(3): Show |
201 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): Show |
311 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(308): Show |
intron_variant | MODIFIER | c.138-4532_138-4523d others(12): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150617838 | ||||||
| chr3:150617838 | T | TGTTTGGT others(8): Show |
5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG00741.hp1 HG02683.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-4537_138-4523d others(17): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150617838 | ||||||
| chr3:150617838 | T | TTGTTTGG others(4): Show |
1 | a0001c0001t0001g0239 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.138-4547_138-4546i others(13): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150617838 | |||||||
| chr3:150618154 | C | G | 1 | a0001c0001t0016g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-4231C>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150618154 | |||||||
| chr3:150618209 | C | T | 9 | a0001c0001t0006g0131 a0001c0001t0006g0132 a0001c0001t0006g0133 others(6): Show |
10 | HG02109.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.138-4176C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150618209 | |||||||
| chr3:150618263 | G | T | 4 | a0001c0001t0003g0040 a0001c0001t0003g0163 a0001c0001t0003g0164 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-4122G>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150618263 | |||||||
| chr3:150618314 | C | T | 1 | a0001c0001t0003g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.138-4071C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150618314 | |||||||
| chr3:150618651 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.138-3734A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150618651 | |||||||
| chr3:150618703 | T | A | 1 | a0001c0001t0003g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.138-3682T>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150618703 | |||||||
| chr3:150618721 | A | G | 1 | a0001c0001t0003g0230 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.138-3664A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150618721 | |||||||
| chr3:150618742 | T | G | 1 | a0001c0001t0021g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.138-3643T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150618742 | |||||||
| chr3:150619040 | T | G | 5 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(2): Show |
5 | NA18974.hp1 NA19009.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-3345T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150619040 | |||||||
| chr3:150619056 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.138-3329T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150619056 | |||||||
| chr3:150619097 | T | C | 5 | a0001c0001t0003g0058 a0001c0001t0003g0224 a0001c0001t0003g0225 others(2): Show |
5 | HG01175.hp2 HG02300.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-3288T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150619097 | |||||||
| chr3:150619104 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(224): Show |
341 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.138-3281T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150619104 | |||||||
| chr3:150619220 | C | CA | 102 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0098 others(99): Show |
145 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.138-3147dupA | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150619220 | ||||||
| chr3:150619220 | C | CAA | 10 | a0001c0001t0002g0150 a0001c0001t0002g0153 a0001c0001t0002g0172 others(7): Show |
10 | HG01981.hp1 HG03017.hp2 HG03209.hp2 others(7): Show |
intron_variant | MODIFIER | c.138-3148_138-3147d others(4): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150619220 | ||||||
| chr3:150619234 | A | G | 1 | a0001c0001t0004g0138 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.138-3151A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150619234 | |||||||
| chr3:150619426 | T | G | 1 | a0001c0001t0001g0087 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.138-2959T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150619426 | |||||||
| chr3:150619554 | T | C | 1 | a0001c0001t0016g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-2831T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150619554 | |||||||
| chr3:150619583 | A | G | 5 | a0001c0001t0003g0058 a0001c0001t0003g0224 a0001c0001t0003g0225 others(2): Show |
5 | HG01175.hp2 HG02300.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-2802A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150619583 | |||||||
| chr3:150619904 | G | A | 1 | a0001c0001t0021g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.138-2481G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150619904 | |||||||
| chr3:150620013 | T | G | 1 | a0001c0001t0002g0189 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.138-2372T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150620013 | |||||||
| chr3:150620227 | C | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(1): Show |
4 | HG00741.hp1 HG02683.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-2158C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150620227 | |||||||
| chr3:150620712 | C | G | 1 | a0001c0001t0027g0093 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.138-1673C>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150620712 | |||||||
| chr3:150621086 | G | T | 1 | a0001c0001t0006g0133 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.138-1299G>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150621086 | |||||||
| chr3:150621187 | G | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0106 a0001c0001t0001g0110 others(2): Show |
8 | NA18944.hp1 NA18947.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.138-1198G>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150621187 | |||||||
| chr3:150621275 | C | A | 1 | a0001c0001t0003g0229 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.138-1110C>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150621275 | |||||||
| chr3:150621278 | A | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(83): Show |
146 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.138-1107A>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150621278 | |||||||
| chr3:150621374 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(204): Show |
317 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.138-1011T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150621374 | |||||||
| chr3:150621570 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.138-815A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150621570 | |||||||
| chr3:150621614 | C | CT | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
172 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.138-749dupT | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150621614 | ||||||
| chr3:150621614 | C | CTT | 82 | a0001c0001t0001g0056 a0001c0001t0001g0072 a0001c0001t0001g0081 others(79): Show |
115 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(112): Show |
intron_variant | MODIFIER | c.138-750_138-749dup others(2): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150621614 | ||||||
| chr3:150621614 | C | CTTT | 20 | a0001c0001t0002g0014 a0001c0001t0002g0044 a0001c0001t0002g0048 others(17): Show |
25 | HG00609.hp1 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.138-751_138-749dup others(3): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150621614 | ||||||
| chr3:150621614 | CTT | C | 14 | a0001c0001t0003g0024 a0001c0001t0003g0058 a0001c0001t0003g0224 others(11): Show |
17 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.138-750_138-749del others(2): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 150621614 | ||||||
| chr3:150621751 | C | T | 1 | a0001c0001t0003g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.138-634C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150621751 | |||||||
| chr3:150622017 | A | C | 1 | a0001c0001t0002g0219 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.138-368A>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150622017 | |||||||
| chr3:150622178 | A | G | 2 | a0001c0001t0004g0137 a0001c0001t0004g0148 |
2 | HG00323.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.138-207A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150622178 | |||||||
| chr3:150622327 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(116): Show |
192 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.138-58A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 1/5 | chr3 | 150622327 | |||||||
| chr3:150622547 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.248+52T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 2/5 | chr3 | 150622547 | |||||||
| chr3:150622571 | T | C | 3 | a0001c0001t0004g0021 a0001c0001t0004g0145 a0001c0001t0004g0146 |
5 | HG01884.hp2 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.248+76T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 2/5 | chr3 | 150622571 | |||||||
| chr3:150622703 | G | A | 3 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 |
3 | HG01243.hp2 HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.248+208G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 2/5 | chr3 | 150622703 | |||||||
| chr3:150622920 | T | A | 5 | a0001c0001t0003g0058 a0001c0001t0003g0224 a0001c0001t0003g0225 others(2): Show |
5 | HG01175.hp2 HG02300.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.249-123T>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 2/5 | chr3 | 150622920 | |||||||
| chr3:150623282 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.375+113A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 3/5 | chr3 | 150623282 | |||||||
| chr3:150623359 | A | G | 1 | a0001c0001t0003g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.375+190A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 3/5 | chr3 | 150623359 | |||||||
| chr3:150623377 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(204): Show |
317 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.375+208T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 3/5 | chr3 | 150623377 | |||||||
| chr3:150623480 | C | T | 1 | a0001c0001t0016g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.375+311C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 3/5 | chr3 | 150623480 | |||||||
| chr3:150623553 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.375+384T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 3/5 | chr3 | 150623553 | |||||||
| chr3:150623988 | C | T | 9 | a0001c0001t0006g0131 a0001c0001t0006g0132 a0001c0001t0006g0133 others(6): Show |
10 | HG02109.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.375+819C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 3/5 | chr3 | 150623988 | |||||||
| chr3:150624055 | G | GT | 20 | a0001c0001t0004g0007 a0001c0001t0004g0020 a0001c0001t0004g0021 others(17): Show |
31 | HG00323.hp1 HG00735.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.376-756dupT | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 150624055 | ||||||
| chr3:150624093 | T | C | 4 | a0001c0001t0002g0043 a0001c0001t0002g0185 a0001c0001t0002g0198 others(1): Show |
5 | HG00609.hp1 HG02040.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.376-719T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 3/5 | chr3 | 150624093 | |||||||
| chr3:150624147 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.376-665G>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 3/5 | chr3 | 150624147 | |||||||
| chr3:150624544 | A | C | 1 | a0001c0001t0003g0227 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.376-268A>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 3/5 | chr3 | 150624544 | |||||||
| chr3:150624610 | C | T | 13 | a0001c0001t0004g0007 a0001c0001t0004g0020 a0001c0001t0004g0034 others(10): Show |
20 | HG00323.hp1 HG00735.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.376-202C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 3/5 | chr3 | 150624610 | |||||||
| chr3:150624647 | C | G | 1 | a0001c0001t0002g0177 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.376-165C>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 3/5 | chr3 | 150624647 | |||||||
| chr3:150624766 | A | C | 3 | a0001c0001t0003g0016 a0001c0001t0003g0026 a0001c0001t0003g0066 |
6 | HG00639.hp1 HG00642.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.376-46A>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 3/5 | chr3 | 150624766 | |||||||
| chr3:150625067 | CT | C | 19 | a0001c0001t0004g0007 a0001c0001t0004g0020 a0001c0001t0004g0021 others(16): Show |
29 | HG00323.hp1 HG00735.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.463+180delT | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 150625067 | ||||||
| chr3:150625101 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.463+202C>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | chr3 | 150625101 | |||||||
| chr3:150625108 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(200): Show |
313 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(310): Show |
intron_variant | MODIFIER | c.463+209T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | chr3 | 150625108 | |||||||
| chr3:150625687 | A | G | 3 | a0001c0001t0006g0131 a0001c0001t0006g0132 a0001c0001t0006g0134 |
3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.463+788A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | chr3 | 150625687 | |||||||
| chr3:150625812 | A | G | 1 | a0001c0001t0020g0105 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.463+913A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | chr3 | 150625812 | |||||||
| chr3:150625870 | C | CT | 11 | a0001c0001t0001g0121 a0001c0001t0002g0180 a0001c0001t0002g0187 others(8): Show |
12 | HG01891.hp2 HG01952.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.463+988dupT | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 150625870 | ||||||
| chr3:150625870 | C | CTT | 25 | a0001c0001t0004g0007 a0001c0001t0004g0020 a0001c0001t0004g0021 others(22): Show |
36 | HG00323.hp1 HG00735.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.463+987_463+988dup others(2): Show |
SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 150625870 | ||||||
| chr3:150625870 | CT | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(83): Show |
146 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.463+988delT | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 150625870 | ||||||
| chr3:150625901 | G | A | 1 | a0001c0001t0009g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.463+1002G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | chr3 | 150625901 | |||||||
| chr3:150625909 | G | A | 1 | a0001c0001t0002g0042 | 2 | HG01516.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.463+1010G>A | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | chr3 | 150625909 | |||||||
| chr3:150625996 | C | T | 1 | a0001c0001t0003g0039 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.464-1014C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | chr3 | 150625996 | |||||||
| chr3:150626037 | T | C | 2 | a0001c0001t0003g0025 a0001c0001t0003g0064 |
3 | HG01255.hp1 HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.464-973T>C | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | chr3 | 150626037 | |||||||
| chr3:150626198 | A | G | 1 | a0001c0001t0002g0216 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.464-812A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | chr3 | 150626198 | |||||||
| chr3:150626536 | C | T | 1 | a0001c0001t0016g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.464-474C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | chr3 | 150626536 | |||||||
| chr3:150626688 | A | T | 1 | a0001c0001t0002g0201 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.464-322A>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | chr3 | 150626688 | |||||||
| chr3:150626867 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0104 |
3 | HG01081.hp1 HG01256.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.464-143A>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 4/5 | chr3 | 150626867 | |||||||
| chr3:150627237 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.*29+74C>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 5/5 | chr3 | 150627237 | |||||||
| chr3:150627289 | T | G | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0090 |
3 | HG00423.hp2 HG00438.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.*29+126T>G | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 5/5 | chr3 | 150627289 | |||||||
| chr3:150627488 | G | T | 5 | a0001c0001t0003g0058 a0001c0001t0003g0224 a0001c0001t0003g0225 others(2): Show |
5 | HG01175.hp2 HG02300.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.*30-171G>T | SELENOT | ENSG00000198843.14 | transcript | ENST00000471696.6 | protein_coding | 5/5 | chr3 | 150627488 |