Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83642 |
| ensemblid | ENSG00000073169.15 |
| hgncid | 30395 |
| symbol | SELENOO |
| name | selenoprotein O |
| refseq_nuc | NM_031454.2 |
| refseq_prot | NP_113642.1 |
| ensembl_nuc | ENST00000380903.7 |
| ensembl_prot | ENSP00000370288.2 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 50201011 |
| end | 50217616 |
| strand | + |
| ver | v1.2 |
| region | chr22:50201011-50217616 |
| region5000 | chr22:50196011-50222616 |
| regionname0 | SELENOO_chr22_50201011_50217616 |
| regionname5000 | SELENOO_chr22_50196011_50222616 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 666 | 209 | 47 | 34 | 95 | 7 | 25 | 74 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0002 | 1/0 | 666 | 175 | 20 | 35 | 92 | 10 | 17 | 73 | SELENOO_chr22_50196011_50222616 | SELENOO | MAVYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0003 | 0/0 | 666 | 15 | 12 | 3 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0004 | 0/0 | 666 | 13 | 0 | 0 | 10 | 0 | 3 | 7 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0005 | 0/0 | 666 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0006 | 0/0 | 666 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | MAVYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0007 | 0/0 | 666 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0008 | 0/0 | 666 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0009 | 0/0 | 666 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0010 | 0/0 | 666 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0011 | 0/0 | 666 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0012 | 0/0 | 666 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0013 | 0/0 | 666 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0014 | 0/0 | 666 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0015 | 0/0 | 666 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0016 | 0/0 | 666 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0017 | 0/0 | 666 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | MAAYR others(661): Show |
chr22 | 50196011 | 50222616 |
| a0018 | 0/0 | 666 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | MAVYR others(661): Show |
chr22 | 50196011 | 50222616 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2007 | 195 | 39 | 30 | 95 | 6 | 24 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0001c0006 | 0/0 | 2007 | 3 | 2 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0001c0007 | 0/0 | 2007 | 3 | 2 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0001c0008 | 0/0 | 2007 | 3 | 0 | 1 | 0 | 1 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0001c0011 | 0/0 | 2007 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0001c0016 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0001c0022 | 0/0 | 2007 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0001c0023 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0002c0002 | 1/0 | 2007 | 167 | 16 | 35 | 90 | 9 | 16 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0002c0009 | 0/0 | 2007 | 3 | 3 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0002c0012 | 0/0 | 2007 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0002c0027 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0002c0029 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0002c0030 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0003c0003 | 0/0 | 2007 | 15 | 12 | 3 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0004c0004 | 0/0 | 2007 | 13 | 0 | 0 | 10 | 0 | 3 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0005c0005 | 0/0 | 2007 | 11 | 11 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0006c0013 | 0/0 | 2007 | 2 | 0 | 1 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0007c0010 | 0/0 | 2007 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0008c0020 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0009c0015 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0010c0019 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0011c0018 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0012c0021 | 0/0 | 2007 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0013c0017 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0014c0026 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0015c0025 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0016c0014 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0017c0024 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 | ||
| a0018c0028 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | ATGGC others(2002): Show |
chr22 | 50196011 | 50222616 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2283 | 195 | 39 | 30 | 95 | 6 | 24 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0001c0006t0001 | 0/0 | 2283 | 3 | 2 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0001c0007t0001 | 0/0 | 2283 | 3 | 2 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0001c0008t0001 | 0/0 | 2283 | 3 | 0 | 1 | 0 | 1 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0001c0011t0001 | 0/0 | 2283 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0001c0016t0001 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0001c0022t0001 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0001c0023t0001 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0002c0002t0001 | 1/0 | 2283 | 132 | 16 | 35 | 55 | 9 | 16 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0002c0002t0002 | 0/0 | 2283 | 26 | 0 | 0 | 26 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0002c0002t0004 | 0/0 | 2283 | 9 | 0 | 0 | 9 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0002c0009t0005 | 0/0 | 2283 | 3 | 3 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0002c0012t0001 | 0/0 | 2283 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0002c0027t0001 | 0/0 | 2283 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0002c0029t0001 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0002c0030t0001 | 0/0 | 2283 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0003c0003t0001 | 0/0 | 2283 | 5 | 3 | 2 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0003c0003t0003 | 0/0 | 2283 | 10 | 9 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0004c0004t0001 | 0/0 | 2283 | 13 | 0 | 0 | 10 | 0 | 3 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0005c0005t0001 | 0/0 | 2283 | 11 | 11 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0006c0013t0001 | 0/0 | 2283 | 2 | 0 | 1 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0007c0010t0001 | 0/0 | 2283 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0008c0020t0001 | 0/0 | 2283 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0009c0015t0001 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0010c0019t0001 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0011c0018t0001 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0012c0021t0001 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0013c0017t0001 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0014c0026t0001 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0015c0025t0001 | 0/0 | 2283 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0016c0014t0001 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0017c0024t0001 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| a0018c0028t0001 | 0/0 | 2283 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | GGCTT others(2278): Show |
chr22 | 50196011 | 50222616 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 19 | 0 | 0 | 19 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0004 | 0/0 | 15 | 1 | 7 | 7 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0005 | 0/0 | 12 | 0 | 1 | 7 | 0 | 4 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 2 | 0 | 2 | 4 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0010 | 0/0 | 6 | 1 | 0 | 1 | 0 | 4 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0011 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0012 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0015 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0032 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0006t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0006t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0006t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0007t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0008t0001g0031 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0011t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0016t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0022t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0001c0023t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0001 | 0/0 | 27 | 6 | 7 | 9 | 1 | 4 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0003 | 0/0 | 16 | 0 | 9 | 4 | 1 | 2 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0008 | 1/0 | 10 | 1 | 6 | 0 | 2 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0013 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0016 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0024 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0033 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0034 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0036 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0037 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0054 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0057 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0002g0001 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0004g0018 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0002t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0009t0005g0038 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0012t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0027t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0029t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0002c0030t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0003c0003t0001g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0003c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0003c0003t0003g0006 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0003c0003t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0004c0004t0001g0009 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0004c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0004c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0004c0004t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0004c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0005c0005t0001g0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0005c0005t0001g0023 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0005c0005t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0005c0005t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0005c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0006c0013t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0007c0010t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0008c0020t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0009c0015t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0010c0019t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0011c0018t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0012c0021t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0013c0017t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0014c0026t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0015c0025t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0016c0014t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0017c0024t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| a0018c0028t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0008 | c0020 | t0001 | g0005 | EUR | GBR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0062 | EUR | GBR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0034 | EUR | GBR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00280 | hp1 | a0001 | c0008 | t0001 | g0031 | EUR | FIN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0003 | EUR | FIN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00408 | hp2 | a0004 | c0004 | t0001 | g0009 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00544 | hp1 | a0009 | c0015 | t0001 | g0002 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00597 | hp1 | a0004 | c0004 | t0001 | g0009 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00609 | hp2 | a0002 | c0002 | t0004 | g0035 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0145 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0130 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00741 | hp1 | a0003 | c0003 | t0003 | g0077 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0164 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0006 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0033 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01243 | hp2 | a0001 | c0007 | t0001 | g0007 | AMR | PUR | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01255 | hp2 | a0003 | c0003 | t0001 | g0060 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01346 | hp2 | a0006 | c0013 | t0001 | g0001 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0057 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01361 | hp2 | a0001 | c0006 | t0001 | g0105 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01433 | hp2 | a0001 | c0008 | t0001 | g0031 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0033 | EUR | IBS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01515 | hp2 | a0002 | c0027 | t0001 | g0003 | EUR | IBS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0008 | EUR | IBS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0033 | EUR | IBS | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01891 | hp2 | a0003 | c0003 | t0003 | g0006 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01981 | hp2 | a0001 | c0022 | t0001 | g0100 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02155 | hp1 | a0004 | c0004 | t0001 | g0009 | EAS | CDX | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CDX | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02257 | hp1 | a0001 | c0023 | t0001 | g0061 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02257 | hp2 | a0005 | c0005 | t0001 | g0023 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02280 | hp2 | a0011 | c0018 | t0001 | g0095 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0156 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02300 | hp1 | a0012 | c0021 | t0001 | g0012 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02451 | hp2 | a0005 | c0005 | t0001 | g0022 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0129 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02615 | hp1 | a0005 | c0005 | t0001 | g0022 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02622 | hp2 | a0002 | c0009 | t0005 | g0038 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02647 | hp1 | a0003 | c0003 | t0003 | g0006 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02683 | hp1 | a0002 | c0030 | t0001 | g0003 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02717 | hp1 | a0005 | c0005 | t0001 | g0023 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02717 | hp2 | a0014 | c0026 | t0001 | g0005 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02723 | hp2 | a0002 | c0009 | t0005 | g0038 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02738 | hp2 | a0004 | c0004 | t0001 | g0009 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02809 | hp1 | a0001 | c0011 | t0001 | g0010 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0006 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02895 | hp2 | a0005 | c0005 | t0001 | g0022 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02896 | hp1 | a0003 | c0003 | t0003 | g0006 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02896 | hp2 | a0005 | c0005 | t0001 | g0123 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02897 | hp1 | a0003 | c0003 | t0003 | g0006 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0146 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02922 | hp2 | a0001 | c0007 | t0001 | g0007 | AFR | ESN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02976 | hp1 | a0001 | c0007 | t0001 | g0007 | AFR | ESN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03098 | hp1 | a0002 | c0009 | t0005 | g0038 | AFR | MSL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03130 | hp1 | a0005 | c0005 | t0001 | g0148 | AFR | ESN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03139 | hp1 | a0003 | c0003 | t0003 | g0006 | AFR | ESN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03139 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | ESN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03209 | hp1 | a0003 | c0003 | t0003 | g0006 | AFR | MSL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03225 | hp1 | a0005 | c0005 | t0001 | g0023 | AFR | MSL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03239 | hp1 | a0006 | c0013 | t0001 | g0001 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0167 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03453 | hp1 | a0003 | c0003 | t0003 | g0006 | AFR | MSL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0054 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0054 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ESN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03516 | hp2 | a0005 | c0005 | t0001 | g0023 | AFR | ESN | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03579 | hp2 | a0003 | c0003 | t0003 | g0006 | AFR | MSL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | STU | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03688 | hp2 | a0004 | c0004 | t0001 | g0117 | SAS | STU | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03704 | hp1 | a0001 | c0008 | t0001 | g0031 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03831 | hp1 | a0004 | c0004 | t0001 | g0111 | SAS | BEB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0159 | SAS | BEB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0165 | SAS | STU | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0151 | SAS | STU | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0163 | SAS | STU | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG04199 | hp2 | a0015 | c0025 | t0001 | g0101 | SAS | STU | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0133 | SAS | STU | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | STU | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0157 | SAS | STU | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | YRI | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | YRI | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18943 | hp2 | a0004 | c0004 | t0001 | g0009 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18947 | hp1 | a0002 | c0012 | t0001 | g0014 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18954 | hp1 | a0002 | c0002 | t0004 | g0018 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18960 | hp2 | a0002 | c0002 | t0004 | g0150 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18965 | hp2 | a0004 | c0004 | t0001 | g0115 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18969 | hp2 | a0004 | c0004 | t0001 | g0009 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18971 | hp2 | a0007 | c0010 | t0001 | g0047 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18973 | hp1 | a0004 | c0004 | t0001 | g0118 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18975 | hp1 | a0002 | c0002 | t0004 | g0124 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18981 | hp2 | a0004 | c0004 | t0001 | g0009 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18989 | hp1 | a0002 | c0002 | t0004 | g0035 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18993 | hp2 | a0007 | c0010 | t0001 | g0047 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19007 | hp1 | a0002 | c0002 | t0004 | g0018 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19009 | hp1 | a0002 | c0002 | t0004 | g0018 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19043 | hp1 | a0005 | c0005 | t0001 | g0022 | AFR | LWK | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19057 | hp1 | a0016 | c0014 | t0001 | g0004 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19062 | hp2 | a0017 | c0024 | t0001 | g0005 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19064 | hp1 | a0004 | c0004 | t0001 | g0009 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19067 | hp1 | a0002 | c0012 | t0001 | g0014 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19077 | hp1 | a0002 | c0002 | t0004 | g0018 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19080 | hp2 | a0004 | c0004 | t0001 | g0009 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19091 | hp1 | a0002 | c0002 | t0004 | g0018 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19240 | hp1 | a0001 | c0016 | t0001 | g0011 | AFR | YRI | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ASW | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA20129 | hp2 | a0001 | c0006 | t0001 | g0106 | AFR | ASW | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0008 | EUR | TSI | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | TSI | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0158 | EUR | TSI | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA20905 | hp2 | a0018 | c0028 | t0001 | g0149 | SAS | GIH | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0162 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02109 | hp1 | a0010 | c0019 | t0001 | g0172 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02486 | hp1 | a0001 | c0011 | t0001 | g0010 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02486 | hp2 | a0013 | c0017 | t0001 | g0020 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG03471 | hp2 | a0001 | c0006 | t0001 | g0104 | AFR | MSL | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG06807 | hp1 | a0003 | c0003 | t0003 | g0006 | AFR | USA | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| HG06807 | hp2 | a0005 | c0005 | t0001 | g0147 | AFR | USA | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | USA | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA21309 | hp1 | a0002 | c0029 | t0001 | g0003 | AFR | LWK | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | LWK | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0085 | REF | REF | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0008 | REF | REF | SELENOO_chr22_50196011_50222616 | SELENOO | chr22 | 50196011 | 50222616 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50201044 | T | C | 15 | a0001 a0003 a0004 others(12): Show |
259 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
missense_variant | MODERATE | c.8T>C | p.Val3Ala | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/9 | 34/2283 | 8/2010 | 3/669 | chr22 | 50201044 | |||
| chr22:50201355 | G | A | 1 | a0016 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.319G>A | p.Gly107Ser | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/9 | 345/2283 | 319/2010 | 107/669 | chr22 | 50201355 | |||
| chr22:50201536 | C | A | 14 | a0001 a0003 a0004 others(11): Show |
248 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
missense_variant | MODERATE | c.500C>A | p.Thr167Asn | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/9 | 526/2283 | 500/2010 | 167/669 | chr22 | 50201536 | |||
| chr22:50206438 | G | A | 1 | a0009 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.676G>A | p.Val226Met | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/9 | 702/2283 | 676/2010 | 226/669 | chr22 | 50206438 | |||
| chr22:50206487 | C | T | 1 | a0014 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.725C>T | p.Thr242Met | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/9 | 751/2283 | 725/2010 | 242/669 | chr22 | 50206487 | |||
| chr22:50208657 | G | A | 1 | a0006 | 2 | HG01346.hp2 HG03239.hp1 |
missense_variant | MODERATE | c.880G>A | p.Glu294Lys | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/9 | 906/2283 | 880/2010 | 294/669 | chr22 | 50208657 | |||
| chr22:50210675 | G | A | 1 | a0013 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.1115G>A | p.Arg372His | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/9 | 1141/2283 | 1115/2010 | 372/669 | chr22 | 50210675 | |||
| chr22:50210691 | G | T | 1 | a0017 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.1131G>T | p.Lys377Asn | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/9 | 1157/2283 | 1131/2010 | 377/669 | chr22 | 50210691 | |||
| chr22:50210869 | G | C | 1 | a0015 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1309G>C | p.Gly437Arg | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/9 | 1335/2283 | 1309/2010 | 437/669 | chr22 | 50210869 | |||
| chr22:50216767 | G | A | 1 | a0011 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.1579G>A | p.Ala527Thr | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 7/9 | 1605/2283 | 1579/2010 | 527/669 | chr22 | 50216767 | |||
| chr22:50216947 | CTCCAGAG others(12): Show |
C | 1 | a0001 | 1 | NA18953.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.1689-12_1695delATG others(16): Show |
p.Arg563fs | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 8/9 | 1689/2010 | 563/669 | INFO_REALIGN_3_PRIME | chr22 | 50216947 | |||
| chr22:50217112 | G | A | 1 | a0010 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1829G>A | p.Arg610His | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 8/9 | 1855/2283 | 1829/2010 | 610/669 | chr22 | 50217112 | |||
| chr22:50217114 | G | A | 1 | a0008 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.1831G>A | p.Gly611Arg | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 8/9 | 1857/2283 | 1831/2010 | 611/669 | chr22 | 50217114 | |||
| chr22:50217247 | G | A | 2 | a0004 a0018 |
14 | HG00408.hp2 HG00597.hp1 HG02155.hp1 others(11): Show |
missense_variant | MODERATE | c.1888G>A | p.Glu630Lys | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 9/9 | 1914/2283 | 1888/2010 | 630/669 | chr22 | 50217247 | |||
| chr22:50217271 | G | A | 1 | a0003 | 15 | HG00741.hp1 HG01109.hp1 HG01255.hp2 others(12): Show |
missense_variant | MODERATE | c.1912G>A | p.Glu638Lys | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 9/9 | 1938/2283 | 1912/2010 | 638/669 | chr22 | 50217271 | |||
| chr22:50217343 | G | A | 1 | a0012 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.1984G>A | p.Glu662Lys | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 9/9 | 2010/2283 | 1984/2010 | 662/669 | chr22 | 50217343 | |||
| chr22:50217352 | G | A | 1 | a0007 | 2 | NA18971.hp2 NA18993.hp2 |
missense_variant | MODERATE | c.1993G>A | p.Val665Met | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 9/9 | 2019/2283 | 1993/2010 | 665/669 | chr22 | 50217352 | |||
| chr22:50217614 | C | T | 1 | a0002 | 3 | HG02622.hp2 HG02723.hp2 HG03098.hp1 |
splice_region_variant | LOW | c.*245C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 9/9 | chr22 | 50217614 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50201099 | T | C | 22 | a0001c0001 a0001c0006 a0001c0007 others(19): Show |
259 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
synonymous_variant | LOW | c.63T>C | p.Gly21Gly | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/9 | 89/2283 | 63/2010 | 21/669 | chr22 | 50201099 | |||
| chr22:50201177 | G | A | 1 | a0001c0006 | 3 | HG01361.hp2 HG03471.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.141G>A | p.Gly47Gly | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/9 | 167/2283 | 141/2010 | 47/669 | chr22 | 50201177 | |||
| chr22:50201207 | C | G | 21 | a0001c0001 a0001c0006 a0001c0007 others(18): Show |
248 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
synonymous_variant | LOW | c.171C>G | p.Ala57Ala | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/9 | 197/2283 | 171/2010 | 57/669 | chr22 | 50201207 | |||
| chr22:50201267 | G | A | 1 | a0002c0012 | 2 | NA18947.hp1 NA19067.hp1 |
synonymous_variant | LOW | c.231G>A | p.Val77Val | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/9 | 257/2283 | 231/2010 | 77/669 | chr22 | 50201267 | |||
| chr22:50201349 | T | C | 22 | a0001c0001 a0001c0006 a0001c0007 others(19): Show |
249 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
synonymous_variant | LOW | c.313T>C | p.Leu105Leu | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/9 | 339/2283 | 313/2010 | 105/669 | chr22 | 50201349 | |||
| chr22:50201471 | C | T | 1 | a0002c0030 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.435C>T | p.Phe145Phe | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/9 | 461/2283 | 435/2010 | 145/669 | chr22 | 50201471 | |||
| chr22:50208569 | T | C | 1 | a0001c0016 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.792T>C | p.Asp264Asp | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/9 | 818/2283 | 792/2010 | 264/669 | chr22 | 50208569 | |||
| chr22:50208656 | C | T | 1 | a0001c0011 | 2 | HG02486.hp1 HG02809.hp1 |
synonymous_variant | LOW | c.879C>T | p.Pro293Pro | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/9 | 905/2283 | 879/2010 | 293/669 | chr22 | 50208656 | |||
| chr22:50210252 | C | T | 1 | a0003c0003 | 15 | HG00741.hp1 HG01109.hp1 HG01255.hp2 others(12): Show |
synonymous_variant | LOW | c.1011C>T | p.Thr337Thr | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 4/9 | 1037/2283 | 1011/2010 | 337/669 | chr22 | 50210252 | |||
| chr22:50210679 | C | T | 1 | a0015c0025 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1119C>T | p.Tyr373Tyr | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/9 | 1145/2283 | 1119/2010 | 373/669 | chr22 | 50210679 | |||
| chr22:50210697 | C | T | 1 | a0001c0023 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1137C>T | p.Pro379Pro | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/9 | 1163/2283 | 1137/2010 | 379/669 | chr22 | 50210697 | |||
| chr22:50210868 | C | T | 1 | a0001c0008 | 3 | HG00280.hp1 HG01433.hp2 HG03704.hp1 |
synonymous_variant | LOW | c.1308C>T | p.Asp436Asp | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/9 | 1334/2283 | 1308/2010 | 436/669 | chr22 | 50210868 | |||
| chr22:50217038 | C | T | 1 | a0001c0022 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.1755C>T | p.Arg585Arg | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 8/9 | 1781/2283 | 1755/2010 | 585/669 | chr22 | 50217038 | |||
| chr22:50217059 | G | A | 1 | a0001c0007 | 3 | HG01243.hp2 HG02922.hp2 HG02976.hp1 |
synonymous_variant | LOW | c.1776G>A | p.Pro592Pro | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 8/9 | 1802/2283 | 1776/2010 | 592/669 | chr22 | 50217059 | |||
| chr22:50217098 | C | T | 1 | a0002c0029 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1815C>T | p.Ile605Ile | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 8/9 | 1841/2283 | 1815/2010 | 605/669 | chr22 | 50217098 | |||
| chr22:50217294 | G | A | 1 | a0002c0009 | 3 | HG02622.hp2 HG02723.hp2 HG03098.hp1 |
synonymous_variant | LOW | c.1935G>A | p.Ala645Ala | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 9/9 | 1961/2283 | 1935/2010 | 645/669 | chr22 | 50217294 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50217370 | C | T | 1 | a0002c0002t0004 | 9 | HG00609.hp2 NA18954.hp1 NA18960.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 9/9 | 1 | chr22 | 50217370 | ||||||
| chr22:50217393 | C | T | 2 | a0002c0002t0002 a0002c0002t0004 |
35 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*24C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 9/9 | 24 | chr22 | 50217393 | ||||||
| chr22:50217605 | C | T | 1 | a0003c0003t0003 | 10 | HG00741.hp1 HG01891.hp2 HG02647.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*236C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 9/9 | 236 | chr22 | 50217605 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:50201605 | G | A | 1 | a0003c0003t0001g0060 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.554+15G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50201605 | |||||||
| chr22:50201639 | G | A | 1 | a0001c0023t0001g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.554+49G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50201639 | |||||||
| chr22:50201728 | G | A | 1 | a0002c0002t0001g0062 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.554+138G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50201728 | |||||||
| chr22:50201924 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0170 others(5): Show |
15 | HG01243.hp1 HG01496.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.554+334C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50201924 | |||||||
| chr22:50202217 | A | AAAACAAT others(6): Show |
103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
230 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.554+629_554+630ins others(13): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50202217 | ||||||
| chr22:50202217 | A | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(6): Show |
17 | HG01243.hp1 HG01496.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.554+627A>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50202217 | |||||||
| chr22:50202233 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.554+643G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50202233 | |||||||
| chr22:50202234 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.554+644T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50202234 | |||||||
| chr22:50202235 | T | G | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.554+645T>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50202235 | |||||||
| chr22:50202243 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.554+653A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50202243 | |||||||
| chr22:50202247 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.554+657T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50202247 | |||||||
| chr22:50202248 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.554+658A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50202248 | |||||||
| chr22:50202414 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
21 | HG00621.hp2 HG00639.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.554+824C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50202414 | |||||||
| chr22:50202450 | C | T | 1 | a0002c0002t0001g0169 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.554+860C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50202450 | |||||||
| chr22:50202519 | C | G | 1 | a0002c0002t0001g0168 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.554+929C>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50202519 | |||||||
| chr22:50202565 | A | AT | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0002c0002t0001g0057 others(1): Show |
7 | HG01358.hp2 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.554+987dupT | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50202565 | ||||||
| chr22:50202565 | AT | A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0063 a0002c0002t0002g0122 others(2): Show |
6 | HG02896.hp2 NA18953.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.554+987delT | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50202565 | ||||||
| chr22:50202656 | A | G | 1 | a0001c0001t0001g0051 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.554+1066A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50202656 | |||||||
| chr22:50202853 | A | G | 1 | a0002c0002t0001g0167 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.554+1263A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50202853 | |||||||
| chr22:50202903 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.554+1313A>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50202903 | |||||||
| chr22:50202922 | G | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.554+1332G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50202922 | |||||||
| chr22:50203007 | T | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0026 others(9): Show |
26 | HG01934.hp2 HG02004.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.554+1417T>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50203007 | |||||||
| chr22:50203212 | A | G | 1 | a0010c0019t0001g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.554+1622A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50203212 | |||||||
| chr22:50203226 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.554+1636T>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50203226 | |||||||
| chr22:50203487 | C | T | 1 | a0010c0019t0001g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.554+1897C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50203487 | |||||||
| chr22:50203643 | C | T | 5 | a0002c0002t0002g0035 a0002c0002t0004g0018 a0002c0002t0004g0035 others(2): Show |
10 | HG00423.hp2 HG00609.hp2 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.554+2053C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50203643 | |||||||
| chr22:50203891 | CA | C | 11 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0026 others(8): Show |
25 | HG01934.hp2 HG02004.hp2 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.554+2302delA | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50203891 | |||||||
| chr22:50203907 | C | G | 1 | a0001c0001t0001g0051 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.554+2317C>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50203907 | |||||||
| chr22:50203930 | C | T | 27 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0051 others(24): Show |
44 | HG00408.hp2 HG00597.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.554+2340C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50203930 | |||||||
| chr22:50204031 | T | C | 1 | a0001c0001t0001g0052 | 2 | NA18970.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.555-2286T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204031 | |||||||
| chr22:50204061 | G | C | 1 | a0001c0001t0001g0058 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.555-2256G>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204061 | |||||||
| chr22:50204097 | C | T | 9 | a0002c0002t0001g0021 a0002c0002t0001g0055 a0002c0002t0001g0146 others(6): Show |
21 | HG01884.hp1 HG02257.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.555-2220C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204097 | |||||||
| chr22:50204098 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.555-2219G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204098 | |||||||
| chr22:50204119 | G | T | 1 | a0001c0008t0001g0031 | 3 | HG00280.hp1 HG01433.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.555-2198G>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204119 | |||||||
| chr22:50204136 | T | C | 11 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0026 others(8): Show |
25 | HG01934.hp2 HG02004.hp2 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.555-2181T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204136 | |||||||
| chr22:50204309 | C | T | 1 | a0004c0004t0001g0118 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.555-2008C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204309 | |||||||
| chr22:50204310 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG02040.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.555-2007G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204310 | |||||||
| chr22:50204328 | C | T | 2 | a0004c0004t0001g0117 a0018c0028t0001g0149 |
2 | HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.555-1989C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204328 | |||||||
| chr22:50204348 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.555-1969C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204348 | |||||||
| chr22:50204354 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.555-1963C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204354 | |||||||
| chr22:50204364 | C | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.555-1953C>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204364 | |||||||
| chr22:50204597 | G | A | 1 | a0001c0022t0001g0100 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.555-1720G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204597 | |||||||
| chr22:50204620 | CA | C | 48 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(45): Show |
122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.555-1682delA | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50204620 | ||||||
| chr22:50204620 | CAAA | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.555-1684_555-1682d others(5): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50204620 | ||||||
| chr22:50204651 | T | A | 1 | a0001c0001t0001g0069 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.555-1666T>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204651 | |||||||
| chr22:50204767 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.555-1550T>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50204767 | |||||||
| chr22:50205064 | G | GTGGGTCC others(63): Show |
39 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(36): Show |
77 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.555-1182_555-1113d others(72): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50205064 | ||||||
| chr22:50205064 | G | GTGGGTCC others(133): Show |
23 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0032 others(20): Show |
26 | HG01074.hp2 HG01175.hp2 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.555-1252_555-1113d others(142): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50205064 | ||||||
| chr22:50205064 | G | GTGGGTCC others(343): Show |
2 | a0001c0001t0001g0098 a0004c0004t0001g0009 |
6 | HG00597.hp1 HG02129.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.555-1113_555-1112i others(352): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50205064 | ||||||
| chr22:50205064 | GTGGGTCC others(63): Show |
G | 1 | a0002c0002t0001g0127 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.555-1182_555-1113d others(72): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50205064 | ||||||
| chr22:50205111 | C | CGATGGGG others(63): Show |
1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.555-1137_555-1136i others(72): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50205111 | ||||||
| chr22:50205124 | G | T | 1 | a0002c0002t0001g0056 | 2 | NA19003.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.555-1193G>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205124 | |||||||
| chr22:50205144 | G | GGGGCTGG others(62): Show |
1 | a0001c0001t0001g0070 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.555-1113_555-1112i others(71): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50205144 | ||||||
| chr22:50205165 | A | G | 5 | a0005c0005t0001g0022 a0005c0005t0001g0023 a0005c0005t0001g0123 others(2): Show |
11 | HG02257.hp2 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.555-1152A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205165 | |||||||
| chr22:50205200 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
136 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.555-1117G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205200 | |||||||
| chr22:50205200 | G | GTTTCTGG others(62): Show |
1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.555-1113_555-1112i others(71): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50205200 | ||||||
| chr22:50205200 | G | GTTTCTGG others(63): Show |
45 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
89 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.555-1113_555-1112i others(72): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50205200 | ||||||
| chr22:50205200 | G | GTTTCTGG others(133): Show |
12 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0032 others(9): Show |
20 | HG00735.hp1 HG01168.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.555-1113_555-1112i others(142): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50205200 | ||||||
| chr22:50205200 | G | GTTTCTGG others(343): Show |
3 | a0004c0004t0001g0009 a0004c0004t0001g0115 a0004c0004t0001g0118 |
6 | HG00408.hp2 HG02155.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.555-1113_555-1112i others(352): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50205200 | ||||||
| chr22:50205242 | T | C | 3 | a0002c0002t0001g0016 a0002c0002t0001g0125 a0002c0002t0001g0128 |
8 | NA18945.hp2 NA18980.hp2 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.555-1075T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205242 | |||||||
| chr22:50205259 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.555-1058G>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205259 | |||||||
| chr22:50205306 | C | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(6): Show |
17 | HG01243.hp1 HG01496.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.555-1011C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205306 | |||||||
| chr22:50205397 | G | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0026 others(8): Show |
25 | HG01934.hp2 HG02004.hp2 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.555-920G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205397 | |||||||
| chr22:50205410 | C | T | 1 | a0004c0004t0001g0118 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.555-907C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205410 | |||||||
| chr22:50205451 | G | A | 2 | a0001c0001t0001g0173 a0002c0002t0001g0129 |
2 | HG01496.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.555-866G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205451 | |||||||
| chr22:50205490 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.555-827G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205490 | |||||||
| chr22:50205494 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.555-823G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205494 | |||||||
| chr22:50205572 | CAAAA | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0055 a0002c0002t0001g0146 |
7 | HG01884.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.555-741_555-738del others(4): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 50205572 | ||||||
| chr22:50205733 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.555-584C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205733 | |||||||
| chr22:50205748 | G | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(62): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.555-569G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205748 | |||||||
| chr22:50205832 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0170 |
3 | HG02145.hp1 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.555-485G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205832 | |||||||
| chr22:50205878 | A | G | 5 | a0005c0005t0001g0022 a0005c0005t0001g0023 a0005c0005t0001g0123 others(2): Show |
11 | HG02257.hp2 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.555-439A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205878 | |||||||
| chr22:50205937 | C | G | 4 | a0002c0002t0001g0014 a0002c0002t0001g0037 a0002c0002t0001g0166 others(1): Show |
11 | HG00544.hp2 HG02074.hp1 NA18944.hp1 others(8): Show |
intron_variant | MODIFIER | c.555-380C>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205937 | |||||||
| chr22:50205965 | T | G | 3 | a0005c0005t0001g0022 a0005c0005t0001g0123 a0005c0005t0001g0147 |
6 | HG02451.hp2 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.555-352T>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50205965 | |||||||
| chr22:50206015 | G | A | 9 | a0002c0002t0001g0021 a0002c0002t0001g0055 a0002c0002t0001g0146 others(6): Show |
21 | HG01884.hp1 HG02257.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.555-302G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50206015 | |||||||
| chr22:50206051 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
260 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.555-266T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50206051 | |||||||
| chr22:50206229 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0044 others(9): Show |
37 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.555-88G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 1/8 | chr22 | 50206229 | |||||||
| chr22:50206531 | G | C | 1 | a0002c0002t0001g0156 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.758+11G>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50206531 | |||||||
| chr22:50206540 | G | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(62): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.758+20G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50206540 | |||||||
| chr22:50206717 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.758+197C>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50206717 | |||||||
| chr22:50206790 | G | A | 27 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0051 others(24): Show |
44 | HG00408.hp2 HG00597.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.758+270G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50206790 | |||||||
| chr22:50206812 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.758+292C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50206812 | |||||||
| chr22:50206892 | T | TG | 61 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(58): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.758+379dupG | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 50206892 | ||||||
| chr22:50206893 | G | C | 17 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0026 others(14): Show |
35 | HG00423.hp1 HG01884.hp2 HG01934.hp2 others(32): Show |
intron_variant | MODIFIER | c.758+373G>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50206893 | |||||||
| chr22:50206900 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.758+380A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50206900 | |||||||
| chr22:50206924 | G | C | 1 | a0002c0002t0001g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.758+404G>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50206924 | |||||||
| chr22:50207052 | G | A | 1 | a0002c0009t0005g0038 | 3 | HG02622.hp2 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.758+532G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50207052 | |||||||
| chr22:50207221 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.758+701C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50207221 | |||||||
| chr22:50207232 | C | T | 1 | a0002c0002t0001g0169 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.758+712C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50207232 | |||||||
| chr22:50207424 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.758+904C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50207424 | |||||||
| chr22:50207462 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.758+942G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50207462 | |||||||
| chr22:50207565 | C | T | 2 | a0001c0001t0001g0011 a0001c0016t0001g0011 |
8 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.759-971C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50207565 | |||||||
| chr22:50207767 | T | C | 1 | a0002c0002t0001g0166 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.759-769T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50207767 | |||||||
| chr22:50207773 | G | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.759-763G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50207773 | |||||||
| chr22:50207813 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.759-723A>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50207813 | |||||||
| chr22:50207843 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.759-693G>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50207843 | |||||||
| chr22:50207856 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.759-680G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50207856 | |||||||
| chr22:50207889 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.759-647G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50207889 | |||||||
| chr22:50207918 | G | C | 1 | a0002c0002t0001g0131 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.759-618G>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50207918 | |||||||
| chr22:50207965 | T | C | 2 | a0002c0002t0001g0037 a0002c0002t0001g0166 |
4 | NA18944.hp1 NA18983.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-571T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50207965 | |||||||
| chr22:50208148 | C | T | 3 | a0001c0006t0001g0104 a0001c0006t0001g0105 a0001c0006t0001g0106 |
3 | HG01361.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.759-388C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50208148 | |||||||
| chr22:50208178 | T | G | 1 | a0003c0003t0003g0077 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.759-358T>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50208178 | |||||||
| chr22:50208198 | G | A | 1 | a0002c0002t0001g0132 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.759-338G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50208198 | |||||||
| chr22:50208246 | A | G | 16 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0026 others(13): Show |
33 | HG00423.hp1 HG01934.hp2 HG02004.hp2 others(30): Show |
intron_variant | MODIFIER | c.759-290A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50208246 | |||||||
| chr22:50208285 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.759-251C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50208285 | |||||||
| chr22:50208299 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.759-237G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50208299 | |||||||
| chr22:50208387 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.759-149G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50208387 | |||||||
| chr22:50208430 | CA | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.759-90delA | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 50208430 | ||||||
| chr22:50208507 | G | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.759-29G>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50208507 | |||||||
| chr22:50208513 | G | C | 1 | a0002c0002t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.759-23G>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50208513 | |||||||
| chr22:50208515 | C | T | 1 | a0002c0002t0002g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.759-21C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 2/8 | chr22 | 50208515 | |||||||
| chr22:50208737 | C | T | 1 | a0001c0001t0001g0050 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.939+21C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50208737 | |||||||
| chr22:50208827 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0094 |
4 | HG02109.hp2 HG02809.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+111C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50208827 | |||||||
| chr22:50208845 | C | T | 16 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0026 others(13): Show |
33 | HG00423.hp1 HG01934.hp2 HG02004.hp2 others(30): Show |
intron_variant | MODIFIER | c.939+129C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50208845 | |||||||
| chr22:50208862 | C | A | 1 | a0001c0001t0001g0043 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.939+146C>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50208862 | |||||||
| chr22:50208946 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.939+230C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50208946 | |||||||
| chr22:50208981 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0044 a0001c0001t0001g0071 |
9 | HG02080.hp2 HG02083.hp1 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.939+265G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50208981 | |||||||
| chr22:50209019 | T | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0063 others(14): Show |
25 | HG00735.hp1 HG01074.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.939+303T>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209019 | |||||||
| chr22:50209202 | G | A | 1 | a0004c0004t0001g0115 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.939+486G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209202 | |||||||
| chr22:50209301 | C | G | 1 | a0001c0001t0001g0050 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.939+585C>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209301 | |||||||
| chr22:50209345 | C | T | 1 | a0001c0001t0001g0051 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.939+629C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209345 | |||||||
| chr22:50209464 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.940-717C>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209464 | |||||||
| chr22:50209497 | G | A | 1 | a0002c0002t0001g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.940-684G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209497 | |||||||
| chr22:50209537 | A | G | 123 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0017 others(120): Show |
263 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.940-644A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209537 | |||||||
| chr22:50209540 | C | T | 41 | a0002c0002t0001g0001 a0002c0002t0001g0016 a0002c0002t0001g0033 others(38): Show |
103 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.940-641C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209540 | |||||||
| chr22:50209573 | T | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(29): Show |
75 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.940-608T>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209573 | |||||||
| chr22:50209581 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.940-600A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209581 | |||||||
| chr22:50209602 | G | A | 1 | a0002c0002t0001g0158 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.940-579G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209602 | |||||||
| chr22:50209670 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.940-511G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209670 | |||||||
| chr22:50209694 | C | T | 1 | a0002c0002t0002g0144 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.940-487C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209694 | |||||||
| chr22:50209759 | C | A | 1 | a0002c0002t0001g0131 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.940-422C>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209759 | |||||||
| chr22:50209793 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.940-388G>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209793 | |||||||
| chr22:50209794 | G | T | 6 | a0001c0001t0001g0098 a0004c0004t0001g0009 a0004c0004t0001g0111 others(3): Show |
14 | HG00408.hp2 HG00597.hp1 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.940-387G>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50209794 | |||||||
| chr22:50210000 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.940-181C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50210000 | |||||||
| chr22:50210030 | G | A | 1 | a0001c0023t0001g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.940-151G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50210030 | |||||||
| chr22:50210052 | C | G | 1 | a0001c0008t0001g0031 | 3 | HG00280.hp1 HG01433.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.940-129C>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50210052 | |||||||
| chr22:50210053 | G | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
13 | HG00323.hp2 HG01106.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.940-128G>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50210053 | |||||||
| chr22:50210128 | G | T | 1 | a0002c0002t0002g0143 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.940-53G>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50210128 | |||||||
| chr22:50210148 | C | T | 35 | a0002c0002t0001g0001 a0002c0002t0001g0016 a0002c0002t0001g0033 others(32): Show |
89 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.940-33C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 3/8 | chr22 | 50210148 | |||||||
| chr22:50210360 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1070+49T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 4/8 | chr22 | 50210360 | |||||||
| chr22:50210363 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(6): Show |
17 | HG01243.hp1 HG01496.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1070+52G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 4/8 | chr22 | 50210363 | |||||||
| chr22:50210411 | G | T | 3 | a0001c0006t0001g0104 a0001c0006t0001g0105 a0001c0006t0001g0106 |
3 | HG01361.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1070+100G>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 4/8 | chr22 | 50210411 | |||||||
| chr22:50210555 | C | T | 2 | a0002c0002t0001g0055 a0002c0002t0001g0146 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1071-76C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 4/8 | chr22 | 50210555 | |||||||
| chr22:50210559 | T | G | 2 | a0002c0002t0002g0134 a0002c0002t0002g0135 |
2 | HG00408.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1071-72T>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 4/8 | chr22 | 50210559 | |||||||
| chr22:50210582 | C | T | 1 | a0002c0002t0001g0155 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1071-49C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 4/8 | chr22 | 50210582 | |||||||
| chr22:50210926 | C | T | 1 | a0001c0001t0001g0027 | 3 | HG01934.hp2 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1351+15C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50210926 | |||||||
| chr22:50210927 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1351+16G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50210927 | |||||||
| chr22:50211106 | C | T | 2 | a0002c0002t0004g0018 a0002c0002t0004g0124 |
6 | NA18954.hp1 NA18975.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.1351+195C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211106 | |||||||
| chr22:50211116 | A | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1351+205A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211116 | |||||||
| chr22:50211131 | C | G | 71 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(68): Show |
173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1351+220C>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211131 | |||||||
| chr22:50211180 | A | C | 1 | a0002c0002t0001g0164 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1351+269A>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211180 | |||||||
| chr22:50211212 | T | C | 4 | a0002c0002t0002g0126 a0002c0002t0002g0136 a0002c0002t0002g0142 others(1): Show |
4 | NA18940.hp1 NA19056.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351+301T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211212 | |||||||
| chr22:50211224 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0089 others(2): Show |
9 | HG02109.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1351+313G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211224 | |||||||
| chr22:50211255 | C | T | 1 | a0005c0005t0001g0147 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1351+344C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211255 | |||||||
| chr22:50211281 | C | T | 1 | a0002c0009t0005g0038 | 3 | HG02622.hp2 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1351+370C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211281 | |||||||
| chr22:50211435 | C | T | 1 | a0002c0002t0001g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1351+524C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211435 | |||||||
| chr22:50211441 | G | A | 5 | a0005c0005t0001g0022 a0005c0005t0001g0023 a0005c0005t0001g0123 others(2): Show |
11 | HG02257.hp2 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1351+530G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211441 | |||||||
| chr22:50211442 | A | T | 5 | a0005c0005t0001g0022 a0005c0005t0001g0023 a0005c0005t0001g0123 others(2): Show |
11 | HG02257.hp2 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1351+531A>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211442 | |||||||
| chr22:50211601 | T | C | 1 | a0002c0002t0001g0137 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1351+690T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211601 | |||||||
| chr22:50211621 | A | G | 2 | a0002c0002t0001g0055 a0002c0002t0001g0146 |
3 | HG01884.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1351+710A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211621 | |||||||
| chr22:50211743 | G | A | 4 | a0003c0003t0001g0006 a0003c0003t0001g0060 a0003c0003t0003g0006 others(1): Show |
15 | HG00741.hp1 HG01109.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1351+832G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211743 | |||||||
| chr22:50211847 | G | A | 1 | a0002c0002t0001g0158 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1351+936G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211847 | |||||||
| chr22:50211853 | G | A | 2 | a0001c0001t0001g0020 a0013c0017t0001g0020 |
4 | HG02486.hp2 HG02572.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351+942G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211853 | |||||||
| chr22:50211990 | A | C | 1 | a0002c0002t0001g0021 | 4 | HG02559.hp1 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351+1079A>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211990 | |||||||
| chr22:50211992 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0065 |
3 | HG02040.hp2 HG03704.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1351+1081C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50211992 | |||||||
| chr22:50212044 | A | C | 14 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0027 others(11): Show |
29 | HG00423.hp1 HG01934.hp2 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.1351+1133A>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50212044 | |||||||
| chr22:50212168 | G | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1351+1257G>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50212168 | |||||||
| chr22:50212274 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1351+1363T>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50212274 | |||||||
| chr22:50212665 | G | C | 1 | a0002c0002t0001g0138 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1351+1754G>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50212665 | |||||||
| chr22:50212683 | A | ATGTAAGT others(55): Show |
87 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0017 others(84): Show |
189 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1351+1788_1351+184 others(66): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50212683 | ||||||
| chr22:50212683 | A | ATGTAAGT others(55): Show |
5 | a0001c0001t0001g0063 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | NA18942.hp2 NA18999.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.1351+1811_1351+181 others(66): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50212683 | ||||||
| chr22:50212683 | A | ATGTAAGT others(55): Show |
1 | a0002c0002t0002g0135 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1351+1791_1351+179 others(66): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50212683 | ||||||
| chr22:50212707 | T | TGCCTGTT others(117): Show |
1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1351+1842_1351+184 others(128): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50212707 | ||||||
| chr22:50212707 | T | TGCCTGTT others(117): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0094 |
4 | HG02109.hp2 HG02809.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1351+1849_1351+185 others(128): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50212707 | ||||||
| chr22:50212707 | T | TGCCTGTT others(117): Show |
64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(61): Show |
165 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1351+1849_1351+185 others(128): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50212707 | ||||||
| chr22:50212707 | T | TGCCTGTT others(179): Show |
1 | a0001c0001t0001g0082 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1351+1849_1351+185 others(190): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50212707 | ||||||
| chr22:50212760 | C | CACAGCGT others(55): Show |
1 | a0002c0002t0001g0054 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1351+1849_1351+185 others(66): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50212760 | |||||||
| chr22:50212761 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1351+1850G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50212761 | |||||||
| chr22:50212765 | C | T | 2 | a0001c0001t0001g0042 a0002c0002t0002g0134 |
3 | HG00408.hp1 HG02015.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1351+1854C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50212765 | |||||||
| chr22:50212769 | C | CGCCTGTT others(55): Show |
1 | a0001c0001t0001g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1351+1897_1351+189 others(66): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50212769 | ||||||
| chr22:50212769 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.1351+1858C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50212769 | |||||||
| chr22:50212809 | T | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1351+1898T>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50212809 | |||||||
| chr22:50212849 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1351+1938A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50212849 | |||||||
| chr22:50212868 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1351+1957C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50212868 | |||||||
| chr22:50212911 | A | ATTGTCTC others(55): Show |
1 | a0001c0001t0001g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1351+2018_1351+201 others(66): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50212911 | ||||||
| chr22:50213012 | A | G | 1 | a0001c0006t0001g0106 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1351+2101A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213012 | |||||||
| chr22:50213109 | G | T | 1 | a0002c0002t0001g0169 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1351+2198G>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213109 | |||||||
| chr22:50213125 | A | G | 1 | a0002c0002t0001g0128 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1351+2214A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213125 | |||||||
| chr22:50213136 | C | T | 1 | a0002c0002t0002g0136 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1351+2225C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213136 | |||||||
| chr22:50213256 | TC | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(62): Show |
164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1351+2346delC | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213256 | |||||||
| chr22:50213293 | G | A | 1 | a0004c0004t0001g0117 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1351+2382G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213293 | |||||||
| chr22:50213356 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0113 a0001c0001t0001g0116 |
5 | HG00735.hp1 HG01074.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1352-2361C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213356 | |||||||
| chr22:50213410 | G | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(62): Show |
164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1352-2307G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213410 | |||||||
| chr22:50213512 | G | A | 1 | a0001c0001t0001g0030 | 3 | HG02109.hp2 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1352-2205G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213512 | |||||||
| chr22:50213734 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0058 others(6): Show |
18 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1352-1983A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213734 | |||||||
| chr22:50213772 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0089 others(2): Show |
9 | HG02109.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1352-1945C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213772 | |||||||
| chr22:50213814 | AT | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1352-1896delT | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50213814 | ||||||
| chr22:50213873 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1352-1844C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213873 | |||||||
| chr22:50213883 | C | A | 6 | a0002c0009t0005g0038 a0005c0005t0001g0022 a0005c0005t0001g0023 others(3): Show |
14 | HG02257.hp2 HG02451.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1352-1834C>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213883 | |||||||
| chr22:50213991 | A | C | 1 | a0001c0001t0001g0043 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1352-1726A>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213991 | |||||||
| chr22:50213998 | C | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(31): Show |
92 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.1352-1719C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50213998 | |||||||
| chr22:50214001 | T | C | 1 | a0002c0002t0001g0161 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1352-1716T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214001 | |||||||
| chr22:50214019 | G | A | 1 | a0002c0009t0005g0038 | 3 | HG02622.hp2 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1352-1698G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214019 | |||||||
| chr22:50214109 | ACT | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0055 a0002c0002t0001g0146 |
7 | HG01884.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1352-1605_1352-160 others(6): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50214109 | ||||||
| chr22:50214117 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(31): Show |
78 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1352-1600A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214117 | |||||||
| chr22:50214237 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1352-1480G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214237 | |||||||
| chr22:50214249 | C | T | 1 | a0001c0001t0001g0049 | 2 | HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1352-1468C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214249 | |||||||
| chr22:50214258 | C | T | 1 | a0005c0005t0001g0148 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1352-1459C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214258 | |||||||
| chr22:50214292 | C | G | 2 | a0001c0001t0001g0011 a0001c0016t0001g0011 |
8 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1352-1425C>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214292 | |||||||
| chr22:50214298 | T | C | 1 | a0001c0001t0001g0048 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1352-1419T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214298 | |||||||
| chr22:50214301 | C | T | 1 | a0002c0002t0001g0160 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1352-1416C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214301 | |||||||
| chr22:50214317 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1352-1400T>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214317 | |||||||
| chr22:50214342 | G | A | 6 | a0004c0004t0001g0009 a0004c0004t0001g0111 a0004c0004t0001g0115 others(3): Show |
14 | HG00408.hp2 HG00597.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.1352-1375G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214342 | |||||||
| chr22:50214437 | T | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
166 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1352-1280T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214437 | |||||||
| chr22:50214519 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1352-1198C>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214519 | |||||||
| chr22:50214584 | C | T | 1 | a0001c0001t0001g0053 | 2 | HG02135.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1352-1133C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214584 | |||||||
| chr22:50214589 | G | A | 34 | a0002c0002t0001g0001 a0002c0002t0001g0016 a0002c0002t0001g0054 others(31): Show |
86 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1352-1128G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214589 | |||||||
| chr22:50214591 | A | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0058 others(9): Show |
21 | HG01243.hp1 HG01496.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1352-1126A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214591 | |||||||
| chr22:50214634 | G | A | 2 | a0002c0002t0001g0151 a0002c0002t0001g0159 |
2 | HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1352-1083G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214634 | |||||||
| chr22:50214670 | T | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1352-1047T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214670 | |||||||
| chr22:50214687 | C | A | 1 | a0001c0001t0001g0043 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1352-1030C>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214687 | |||||||
| chr22:50214740 | C | T | 1 | a0002c0002t0001g0141 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1352-977C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214740 | |||||||
| chr22:50214878 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1352-839C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214878 | |||||||
| chr22:50214882 | T | C | 1 | a0001c0001t0001g0044 | 2 | NA18964.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1352-835T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214882 | |||||||
| chr22:50214903 | C | T | 1 | a0001c0001t0001g0050 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1352-814C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50214903 | |||||||
| chr22:50215083 | C | T | 1 | a0001c0001t0001g0049 | 2 | HG01255.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1352-634C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50215083 | |||||||
| chr22:50215142 | CA | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0065 |
3 | HG02040.hp2 HG03704.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1352-574delA | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50215142 | |||||||
| chr22:50215214 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1352-503G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50215214 | |||||||
| chr22:50215405 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1352-312G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50215405 | |||||||
| chr22:50215429 | G | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0065 |
3 | HG02040.hp2 HG03704.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1352-288G>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50215429 | |||||||
| chr22:50215466 | G | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(131): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1352-251G>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50215466 | |||||||
| chr22:50215518 | T | C | 2 | a0001c0001t0001g0043 a0011c0018t0001g0095 |
3 | HG01884.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1352-199T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50215518 | |||||||
| chr22:50215559 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1352-158G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50215559 | |||||||
| chr22:50215635 | T | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0002c0002t0001g0161 others(1): Show |
4 | HG02071.hp2 NA18951.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.1352-82T>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50215635 | |||||||
| chr22:50215635 | T | TG | 80 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
148 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1352-69dupG | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50215635 | ||||||
| chr22:50215635 | T | TGG | 17 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0017 others(14): Show |
26 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.1352-70_1352-69dup others(2): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50215635 | ||||||
| chr22:50215635 | TG | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(25): Show |
36 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1352-69delG | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50215635 | ||||||
| chr22:50215635 | TGG | T | 20 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0040 others(17): Show |
26 | HG01074.hp2 HG01168.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.1352-70_1352-69del others(2): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50215635 | ||||||
| chr22:50215635 | TGGGGGG | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(35): Show |
75 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1352-74_1352-69del others(6): Show |
SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 50215635 | ||||||
| chr22:50215647 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1352-70G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50215647 | |||||||
| chr22:50215662 | A | T | 1 | a0002c0002t0001g0162 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1352-55A>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50215662 | |||||||
| chr22:50215664 | G | T | 1 | a0001c0001t0001g0025 | 3 | NA18992.hp2 NA19004.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1352-53G>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 5/8 | chr22 | 50215664 | |||||||
| chr22:50215876 | T | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0055 a0002c0002t0001g0146 |
7 | HG01884.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1502+9T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50215876 | |||||||
| chr22:50215959 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1502+92T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50215959 | |||||||
| chr22:50215999 | T | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1502+132T>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50215999 | |||||||
| chr22:50216081 | G | C | 1 | a0001c0001t0001g0066 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1502+214G>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216081 | |||||||
| chr22:50216126 | C | T | 2 | a0002c0002t0001g0013 a0002c0002t0001g0156 |
8 | HG01934.hp1 HG01978.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1502+259C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216126 | |||||||
| chr22:50216148 | G | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0027 others(11): Show |
29 | HG00423.hp1 HG01934.hp2 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.1502+281G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216148 | |||||||
| chr22:50216325 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1503-366C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216325 | |||||||
| chr22:50216342 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1503-349G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216342 | |||||||
| chr22:50216368 | T | C | 1 | a0002c0002t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1503-323T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216368 | |||||||
| chr22:50216381 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1503-310A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216381 | |||||||
| chr22:50216419 | C | T | 1 | a0002c0002t0001g0137 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1503-272C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216419 | |||||||
| chr22:50216435 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1503-256T>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216435 | |||||||
| chr22:50216459 | G | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
166 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1503-232G>C | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216459 | |||||||
| chr22:50216474 | G | A | 1 | a0001c0006t0001g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1503-217G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216474 | |||||||
| chr22:50216477 | C | T | 2 | a0004c0004t0001g0117 a0018c0028t0001g0149 |
2 | HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1503-214C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216477 | |||||||
| chr22:50216534 | C | T | 1 | a0001c0001t0001g0051 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1503-157C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216534 | |||||||
| chr22:50216561 | G | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0066 others(2): Show |
9 | HG00438.hp2 HG00558.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1503-130G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216561 | |||||||
| chr22:50216651 | G | A | 1 | a0002c0002t0002g0135 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1503-40G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216651 | |||||||
| chr22:50216669 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1503-22A>G | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 6/8 | chr22 | 50216669 | |||||||
| chr22:50216900 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0071 a0001c0016t0001g0011 |
9 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1688+24C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 7/8 | chr22 | 50216900 | |||||||
| chr22:50216901 | G | A | 1 | a0002c0002t0001g0153 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1688+25G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 7/8 | chr22 | 50216901 | |||||||
| chr22:50216908 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1688+32G>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 7/8 | chr22 | 50216908 | |||||||
| chr22:50216910 | C | T | 1 | a0002c0002t0001g0154 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1688+34C>T | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 7/8 | chr22 | 50216910 | |||||||
| chr22:50216941 | C | A | 1 | a0002c0002t0002g0140 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1689-31C>A | SELENOO | ENSG00000073169.15 | transcript | ENST00000380903.7 | protein_coding | 7/8 | chr22 | 50216941 |