Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6721 |
| ensemblid | ENSG00000198911.13 |
| hgncid | 11290 |
| symbol | SREBF2 |
| name | sterol regulatory element binding transcription factor 2 |
| refseq_nuc | NM_004599.4 |
| refseq_prot | NP_004590.2 |
| ensembl_nuc | ENST00000361204.9 |
| ensembl_prot | ENSP00000354476.4 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 41833105 |
| end | 41907305 |
| strand | + |
| ver | v1.2 |
| region | chr22:41833105-41907305 |
| region5000 | chr22:41828105-41912305 |
| regionname0 | SREBF2_chr22_41833105_41907305 |
| regionname5000 | SREBF2_chr22_41828105_41912305 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1141 | 158 | 21 | 29 | 78 | 11 | 18 | 60 | SREBF2_chr22_41828105_41912305 | SREBF2 | MDDSG others(1136): Show |
chr22 | 41828105 | 41912305 |
| a0002 | 0/0 | 1141 | 136 | 51 | 26 | 42 | 1 | 16 | 34 | SREBF2_chr22_41828105_41912305 | SREBF2 | MDDSG others(1136): Show |
chr22 | 41828105 | 41912305 |
| a0003 | 0/1 | 1141 | 18 | 2 | 4 | 7 | 1 | 3 | 6 | SREBF2_chr22_41828105_41912305 | SREBF2 | MDDSG others(1136): Show |
chr22 | 41828105 | 41912305 |
| a0004 | 0/0 | 1141 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | MDDSG others(1136): Show |
chr22 | 41828105 | 41912305 |
| a0005 | 0/0 | 1141 | 7 | 0 | 1 | 5 | 1 | 0 | 5 | SREBF2_chr22_41828105_41912305 | SREBF2 | MDDSG others(1136): Show |
chr22 | 41828105 | 41912305 |
| a0006 | 0/0 | 1149 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | MDDSG others(1144): Show |
chr22 | 41828105 | 41912305 |
| a0007 | 0/0 | 1141 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | MDDSG others(1136): Show |
chr22 | 41828105 | 41912305 |
| a0008 | 0/0 | 1141 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | MDDSG others(1136): Show |
chr22 | 41828105 | 41912305 |
| a0009 | 0/0 | 1141 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | MDDSG others(1136): Show |
chr22 | 41828105 | 41912305 |
| a0010 | 0/0 | 1141 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | MDDSG others(1136): Show |
chr22 | 41828105 | 41912305 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3423 | 146 | 17 | 25 | 78 | 9 | 16 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0001c0007 | 0/0 | 3423 | 5 | 4 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0001c0011 | 0/0 | 3423 | 2 | 0 | 1 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0001c0012 | 0/0 | 3423 | 2 | 0 | 1 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0001c0020 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0001c0022 | 0/0 | 3423 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0001c0024 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0002c0002 | 0/0 | 3423 | 120 | 39 | 26 | 40 | 1 | 14 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0002c0005 | 0/0 | 3423 | 9 | 9 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0002c0009 | 0/0 | 3423 | 2 | 2 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0002c0013 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0002c0015 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0002c0016 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0002c0018 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0002c0025 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0003c0003 | 0/1 | 3423 | 15 | 0 | 4 | 6 | 1 | 3 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0003c0010 | 0/0 | 3423 | 2 | 1 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0003c0017 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0004c0004 | 0/0 | 3423 | 10 | 10 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0005c0006 | 0/0 | 3423 | 6 | 0 | 1 | 4 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0005c0021 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0006c0008 | 0/0 | 3447 | 3 | 3 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3442): Show |
chr22 | 41828105 | 41912305 | ||
| a0007c0026 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0008c0014 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0009c0019 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 | ||
| a0010c0023 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | ATGGA others(3418): Show |
chr22 | 41828105 | 41912305 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5237 | 121 | 4 | 19 | 73 | 9 | 15 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0001t0002 | 0/0 | 5237 | 2 | 0 | 1 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0001t0003 | 0/0 | 5237 | 9 | 7 | 2 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0001t0004 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0001t0006 | 0/0 | 5244 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5239): Show |
chr22 | 41828105 | 41912305 |
| a0001c0001t0007 | 0/0 | 5237 | 3 | 3 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0001t0011 | 0/0 | 5237 | 2 | 0 | 1 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0001t0012 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0001t0013 | 0/0 | 5233 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CCTTC others(5228): Show |
chr22 | 41828105 | 41912305 |
| a0001c0001t0014 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0001t0016 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0001t0017 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0001t0018 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0001t0019 | 0/0 | 5257 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5252): Show |
chr22 | 41828105 | 41912305 |
| a0001c0007t0003 | 0/0 | 5237 | 5 | 4 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0011t0001 | 0/0 | 5237 | 2 | 0 | 1 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0012t0001 | 0/0 | 5237 | 2 | 0 | 1 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0020t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0022t0001 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0001c0024t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0002c0002t0001 | 0/0 | 5237 | 37 | 1 | 3 | 31 | 0 | 2 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0002c0002t0002 | 0/0 | 5237 | 48 | 9 | 17 | 9 | 1 | 12 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0002c0002t0003 | 0/0 | 5237 | 19 | 15 | 4 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0002c0002t0005 | 0/0 | 5233 | 2 | 2 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5228): Show |
chr22 | 41828105 | 41912305 |
| a0002c0002t0006 | 0/0 | 5244 | 7 | 6 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5239): Show |
chr22 | 41828105 | 41912305 |
| a0002c0002t0007 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0002c0002t0008 | 0/0 | 5233 | 4 | 3 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5228): Show |
chr22 | 41828105 | 41912305 |
| a0002c0002t0012 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0002c0002t0020 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5239): Show |
chr22 | 41828105 | 41912305 |
| a0002c0005t0005 | 0/0 | 5233 | 8 | 8 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5228): Show |
chr22 | 41828105 | 41912305 |
| a0002c0005t0015 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0002c0009t0002 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0002c0013t0001 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0002c0015t0002 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0002c0016t0002 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0002c0018t0004 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0002c0025t0001 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0003c0003t0004 | 0/1 | 5237 | 15 | 0 | 4 | 6 | 1 | 3 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0003c0010t0001 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0003c0010t0021 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0003c0017t0004 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0004c0004t0001 | 0/0 | 5237 | 3 | 3 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0004c0004t0003 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0004c0004t0005 | 0/0 | 5233 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5228): Show |
chr22 | 41828105 | 41912305 |
| a0004c0004t0009 | 0/0 | 5237 | 3 | 3 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0004c0004t0010 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0005c0006t0004 | 0/0 | 5237 | 6 | 0 | 1 | 4 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0005c0021t0001 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0006c0008t0003 | 0/0 | 5261 | 3 | 3 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5256): Show |
chr22 | 41828105 | 41912305 |
| a0007c0026t0001 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0008c0014t0005 | 0/0 | 5233 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5228): Show |
chr22 | 41828105 | 41912305 |
| a0009c0019t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| a0010c0023t0001 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | CTTTC others(5232): Show |
chr22 | 41828105 | 41912305 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0006g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0007g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0011g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0011g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0012g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0013g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0014g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0016g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0017g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0018g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0019g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0007t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0007t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0007t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0007t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0007t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0011t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0011t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0012t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0012t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0020t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0022t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0024t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0008g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0008g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0008g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0008g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0020g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0015g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0009t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0009t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0013t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0015t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0016t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0018t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0025t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0010t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0010t0021g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0017t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0010g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0005c0006t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0005c0006t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0005c0006t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0005c0006t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0005c0006t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0005c0006t0004g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0005c0021t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0006c0008t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0006c0008t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0006c0008t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0007c0026t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0008c0014t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0009c0019t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0010c0023t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0004 | g0136 | EUR | GBR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00099 | hp2 | a0001 | c0020 | t0001 | g0281 | EUR | GBR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | GBR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0274 | EUR | GBR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00280 | hp1 | a0005 | c0006 | t0004 | g0238 | EUR | FIN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0091 | EUR | FIN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0277 | EUR | FIN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00639 | hp1 | a0001 | c0001 | t0014 | g0316 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0150 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0104 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0029 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00741 | hp1 | a0001 | c0011 | t0001 | g0288 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00741 | hp2 | a0002 | c0002 | t0003 | g0076 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01081 | hp1 | a0003 | c0003 | t0004 | g0138 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0101 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0027 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0039 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01109 | hp2 | a0002 | c0002 | t0008 | g0317 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0073 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01169 | hp2 | a0003 | c0003 | t0004 | g0161 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0111 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0093 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01243 | hp1 | a0002 | c0002 | t0006 | g0024 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0066 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0097 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01257 | hp2 | a0001 | c0022 | t0001 | g0280 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0094 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0100 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0105 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01358 | hp1 | a0001 | c0012 | t0001 | g0309 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0063 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0306 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | IBS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0314 | EUR | IBS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01884 | hp1 | a0002 | c0002 | t0005 | g0009 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01891 | hp1 | a0002 | c0002 | t0006 | g0020 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01891 | hp2 | a0002 | c0005 | t0015 | g0248 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01934 | hp2 | a0001 | c0007 | t0003 | g0010 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01943 | hp2 | a0001 | c0001 | t0011 | g0210 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01981 | hp1 | a0003 | c0003 | t0004 | g0130 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0031 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02027 | hp1 | a0003 | c0003 | t0004 | g0106 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02071 | hp1 | a0007 | c0026 | t0001 | g0304 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02129 | hp2 | a0001 | c0001 | t0016 | g0195 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02145 | hp1 | a0002 | c0013 | t0001 | g0226 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02155 | hp2 | a0001 | c0001 | t0011 | g0175 | EAS | CDX | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02257 | hp1 | a0004 | c0004 | t0010 | g0046 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0079 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0208 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02280 | hp1 | a0001 | c0007 | t0003 | g0088 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02280 | hp2 | a0002 | c0002 | t0003 | g0060 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02293 | hp1 | a0005 | c0006 | t0004 | g0299 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0030 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0103 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02300 | hp2 | a0003 | c0003 | t0004 | g0132 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02451 | hp1 | a0002 | c0005 | t0005 | g0243 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02572 | hp1 | a0002 | c0002 | t0006 | g0017 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0109 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0065 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02615 | hp1 | a0002 | c0009 | t0002 | g0223 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02615 | hp2 | a0006 | c0008 | t0003 | g0116 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02622 | hp1 | a0004 | c0004 | t0010 | g0054 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02622 | hp2 | a0002 | c0002 | t0006 | g0023 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02630 | hp1 | a0002 | c0002 | t0003 | g0325 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02630 | hp2 | a0008 | c0014 | t0005 | g0026 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0050 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02647 | hp2 | a0002 | c0002 | t0003 | g0058 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0092 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02683 | hp2 | a0001 | c0011 | t0001 | g0259 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0102 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02717 | hp1 | a0002 | c0002 | t0006 | g0018 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02717 | hp2 | a0002 | c0009 | t0002 | g0205 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02723 | hp2 | a0002 | c0002 | t0003 | g0001 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02735 | hp1 | a0002 | c0016 | t0002 | g0077 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02809 | hp1 | a0006 | c0008 | t0003 | g0114 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02809 | hp2 | a0002 | c0005 | t0005 | g0247 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02818 | hp2 | a0004 | c0004 | t0005 | g0052 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0330 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02886 | hp2 | a0002 | c0002 | t0003 | g0055 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02896 | hp1 | a0004 | c0004 | t0009 | g0048 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0215 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02897 | hp1 | a0002 | c0002 | t0003 | g0056 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02897 | hp2 | a0004 | c0004 | t0009 | g0047 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02965 | hp1 | a0001 | c0007 | t0003 | g0087 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0081 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02970 | hp1 | a0002 | c0002 | t0008 | g0319 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02970 | hp2 | a0001 | c0001 | t0013 | g0216 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03017 | hp1 | a0003 | c0003 | t0004 | g0127 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0160 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03041 | hp1 | a0002 | c0002 | t0003 | g0059 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0113 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03098 | hp1 | a0002 | c0005 | t0005 | g0249 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03098 | hp2 | a0004 | c0004 | t0001 | g0224 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0083 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03130 | hp2 | a0001 | c0007 | t0003 | g0090 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03139 | hp1 | a0002 | c0002 | t0006 | g0019 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03139 | hp2 | a0002 | c0002 | t0003 | g0011 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03195 | hp1 | a0002 | c0002 | t0020 | g0014 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0241 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03225 | hp1 | a0002 | c0002 | t0003 | g0328 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03225 | hp2 | a0003 | c0017 | t0004 | g0044 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03453 | hp1 | a0002 | c0002 | t0008 | g0321 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03453 | hp2 | a0004 | c0004 | t0003 | g0007 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0242 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03486 | hp2 | a0001 | c0007 | t0003 | g0089 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0075 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0074 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03540 | hp2 | a0002 | c0002 | t0003 | g0001 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03579 | hp1 | a0002 | c0005 | t0005 | g0016 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03669 | hp2 | a0003 | c0003 | t0004 | g0096 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0129 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0040 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0061 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0118 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0064 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03942 | hp1 | a0003 | c0003 | t0004 | g0155 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03942 | hp2 | a0009 | c0019 | t0001 | g0098 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04115 | hp1 | a0001 | c0024 | t0001 | g0257 | SAS | STU | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0149 | SAS | STU | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0324 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | STU | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04199 | hp2 | a0002 | c0015 | t0002 | g0068 | SAS | STU | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0148 | SAS | STU | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | STU | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18522 | hp1 | a0002 | c0002 | t0007 | g0329 | AFR | YRI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18522 | hp2 | a0002 | c0002 | t0008 | g0318 | AFR | YRI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | CHB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18906 | hp1 | a0003 | c0010 | t0021 | g0025 | AFR | YRI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18906 | hp2 | a0002 | c0005 | t0005 | g0244 | AFR | YRI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18939 | hp1 | a0003 | c0003 | t0004 | g0124 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18942 | hp1 | a0005 | c0006 | t0004 | g0126 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18952 | hp1 | a0003 | c0003 | t0004 | g0117 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18959 | hp1 | a0003 | c0003 | t0004 | g0142 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18973 | hp2 | a0003 | c0003 | t0004 | g0125 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18978 | hp2 | a0005 | c0006 | t0004 | g0120 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18979 | hp2 | a0002 | c0025 | t0001 | g0140 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18981 | hp1 | a0010 | c0023 | t0001 | g0200 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18986 | hp2 | a0002 | c0018 | t0004 | g0156 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18987 | hp1 | a0005 | c0021 | t0001 | g0258 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18991 | hp2 | a0003 | c0010 | t0001 | g0146 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19004 | hp1 | a0005 | c0006 | t0004 | g0135 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19010 | hp1 | a0001 | c0001 | t0017 | g0173 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19030 | hp1 | a0004 | c0004 | t0001 | g0045 | AFR | LWK | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19030 | hp2 | a0002 | c0002 | t0003 | g0110 | AFR | LWK | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0305 | AFR | LWK | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19043 | hp2 | a0002 | c0002 | t0006 | g0022 | AFR | LWK | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19057 | hp2 | a0005 | c0006 | t0004 | g0134 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19068 | hp1 | a0003 | c0003 | t0004 | g0141 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19068 | hp2 | a0001 | c0001 | t0018 | g0193 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19070 | hp1 | a0001 | c0001 | t0019 | g0176 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19240 | hp1 | a0002 | c0002 | t0012 | g0057 | AFR | YRI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0084 | AFR | YRI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0327 | AFR | ASW | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0082 | AFR | ASW | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20752 | hp1 | a0001 | c0012 | t0001 | g0310 | EUR | TSI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | TSI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0289 | EUR | TSI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | TSI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02109 | hp1 | a0006 | c0008 | t0003 | g0115 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02109 | hp2 | a0002 | c0002 | t0003 | g0078 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02486 | hp1 | a0002 | c0005 | t0005 | g0015 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02486 | hp2 | a0002 | c0005 | t0005 | g0246 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02559 | hp1 | a0002 | c0002 | t0005 | g0051 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02559 | hp2 | a0004 | c0004 | t0009 | g0049 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03471 | hp1 | a0004 | c0004 | t0001 | g0053 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0240 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0095 | AFR | USA | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0080 | AFR | USA | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0145 | AFR | USA | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | USA | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA21309 | hp1 | a0002 | c0005 | t0005 | g0245 | AFR | LWK | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA21309 | hp2 | a0002 | c0002 | t0003 | g0326 | AFR | LWK | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0004 | g0123 | REF | REF | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0222 | REF | REF | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41866925 | T | TAGCAGCA others(17): Show |
1 | a0006 | 3 | HG02109.hp1 HG02615.hp2 HG02809.hp1 |
conservative_inframe_insertion | MODERATE | c.193_216dupGGCAGCAG others(16): Show |
p.Gly65_Ser72dup | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/19 | 383/5237 | 217/3426 | 73/1141 | INFO_REALIGN_3_PRIME | chr22 | 41866925 | ||
| chr22:41867215 | C | G | 1 | a0007 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.473C>G | p.Thr158Ser | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/19 | 639/5237 | 473/3426 | 158/1141 | chr22 | 41867215 | |||
| chr22:41880738 | G | C | 5 | a0002 a0003 a0004 others(2): Show |
165 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(162): Show |
missense_variant | MODERATE | c.1784G>C | p.Gly595Ala | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/19 | 1950/5237 | 1784/3426 | 595/1141 | chr22 | 41880738 | |||
| chr22:41880821 | G | A | 1 | a0004 | 10 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
missense_variant | MODERATE | c.1867G>A | p.Val623Met | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/19 | 2033/5237 | 1867/3426 | 623/1141 | chr22 | 41880821 | |||
| chr22:41884871 | G | A | 1 | a0010 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.2068G>A | p.Asp690Asn | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/19 | 2234/5237 | 2068/3426 | 690/1141 | chr22 | 41884871 | |||
| chr22:41897118 | G | A | 1 | a0008 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.2562G>A | p.Met854Ile | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/19 | 2728/5237 | 2562/3426 | 854/1141 | chr22 | 41897118 | |||
| chr22:41897136 | G | C | 2 | a0003 a0005 |
24 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(21): Show |
missense_variant | MODERATE | c.2580G>C | p.Arg860Ser | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/19 | 2746/5237 | 2580/3426 | 860/1141 | chr22 | 41897136 | |||
| chr22:41900377 | C | T | 1 | a0009 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.2786C>T | p.Ala929Val | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/19 | 2952/5237 | 2786/3426 | 929/1141 | chr22 | 41900377 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41866943 | T | C | 1 | a0002c0013 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.201T>C | p.Ser67Ser | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/19 | 367/5237 | 201/3426 | 67/1141 | chr22 | 41866943 | |||
| chr22:41867108 | C | A | 2 | a0002c0005 a0008c0014 |
10 | HG01891.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
synonymous_variant | LOW | c.366C>A | p.Pro122Pro | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/19 | 532/5237 | 366/3426 | 122/1141 | chr22 | 41867108 | |||
| chr22:41868771 | G | A | 1 | a0001c0007 | 5 | HG01934.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
synonymous_variant | LOW | c.699G>A | p.Ala233Ala | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/19 | 865/5237 | 699/3426 | 233/1141 | chr22 | 41868771 | |||
| chr22:41875637 | C | T | 1 | a0002c0025 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.1299C>T | p.Pro433Pro | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/19 | 1465/5237 | 1299/3426 | 433/1141 | chr22 | 41875637 | |||
| chr22:41877309 | C | T | 1 | a0007c0026 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.1467C>T | p.Phe489Phe | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 8/19 | 1633/5237 | 1467/3426 | 489/1141 | chr22 | 41877309 | |||
| chr22:41877330 | C | T | 1 | a0001c0024 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.1488C>T | p.Pro496Pro | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 8/19 | 1654/5237 | 1488/3426 | 496/1141 | chr22 | 41877330 | |||
| chr22:41878030 | G | T | 1 | a0001c0012 | 2 | HG01358.hp1 NA20752.hp1 |
synonymous_variant | LOW | c.1668G>T | p.Leu556Leu | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/19 | 1834/5237 | 1668/3426 | 556/1141 | chr22 | 41878030 | |||
| chr22:41878072 | C | T | 1 | a0010c0023 | 1 | NA18981.hp1 | synonymous_variant | LOW | c.1710C>T | p.Ser570Ser | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/19 | 1876/5237 | 1710/3426 | 570/1141 | chr22 | 41878072 | |||
| chr22:41878096 | G | C | 1 | a0002c0015 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1734G>C | p.Arg578Arg | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/19 | 1900/5237 | 1734/3426 | 578/1141 | chr22 | 41878096 | |||
| chr22:41880853 | G | A | 1 | a0001c0020 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.1899G>A | p.Leu633Leu | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/19 | 2065/5237 | 1899/3426 | 633/1141 | chr22 | 41880853 | |||
| chr22:41880898 | G | A | 1 | a0002c0016 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.1944G>A | p.Thr648Thr | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/19 | 2110/5237 | 1944/3426 | 648/1141 | chr22 | 41880898 | |||
| chr22:41884885 | G | A | 2 | a0001c0011 a0001c0024 |
3 | HG00741.hp1 HG02683.hp2 HG04115.hp1 |
synonymous_variant | LOW | c.2082G>A | p.Ala694Ala | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/19 | 2248/5237 | 2082/3426 | 694/1141 | chr22 | 41884885 | |||
| chr22:41894863 | G | A | 1 | a0002c0009 | 2 | HG02615.hp1 HG02717.hp2 |
synonymous_variant | LOW | c.2421G>A | p.Leu807Leu | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/19 | 2587/5237 | 2421/3426 | 807/1141 | chr22 | 41894863 | |||
| chr22:41904944 | C | A | 4 | a0002c0018 a0003c0003 a0003c0017 others(1): Show |
22 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(19): Show |
synonymous_variant | LOW | c.3175C>A | p.Arg1059Arg | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 18/19 | 3341/5237 | 3175/3426 | 1059/1141 | chr22 | 41904944 | |||
| chr22:41905531 | G | A | 1 | a0001c0022 | 1 | HG01257.hp2 | synonymous_variant | LOW | c.3297G>A | p.Pro1099Pro | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 3463/5237 | 3297/3426 | 1099/1141 | chr22 | 41905531 | |||
| chr22:41905567 | C | A | 1 | a0003c0017 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.3333C>A | p.Arg1111Arg | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 3499/5237 | 3333/3426 | 1111/1141 | chr22 | 41905567 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41833106 | T | C | 1 | a0001c0001t0013 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-165T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/19 | 165 | chr22 | 41833106 | ||||||
| chr22:41905708 | T | C | 6 | a0001c0001t0002 a0001c0001t0014 a0002c0002t0002 others(3): Show |
55 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*48T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 48 | chr22 | 41905708 | ||||||
| chr22:41905744 | A | G | 17 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(14): Show |
54 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*84A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 84 | chr22 | 41905744 | ||||||
| chr22:41905811 | C | G | 1 | a0002c0002t0008 | 4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*151C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 151 | chr22 | 41905811 | ||||||
| chr22:41905866 | G | A | 1 | a0002c0005t0015 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*206G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 206 | chr22 | 41905866 | ||||||
| chr22:41905919 | A | G | 1 | a0003c0010t0021 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*259A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 259 | chr22 | 41905919 | ||||||
| chr22:41905939 | C | T | 6 | a0001c0001t0004 a0002c0018t0004 a0003c0003t0004 others(3): Show |
24 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*279C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 279 | chr22 | 41905939 | ||||||
| chr22:41905993 | C | T | 2 | a0001c0001t0012 a0002c0002t0012 |
2 | HG02896.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*333C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 333 | chr22 | 41905993 | ||||||
| chr22:41906162 | G | A | 1 | a0002c0002t0020 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*502G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 502 | chr22 | 41906162 | ||||||
| chr22:41906182 | T | TCTGCGTT others(13): Show |
1 | a0001c0001t0019 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*526_*545dupCGTTCC others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 546 | INFO_REALIGN_3_PRIME | chr22 | 41906182 | |||||
| chr22:41906281 | T | TGGTGGGA others(4): Show |
3 | a0001c0001t0006 a0002c0002t0006 a0002c0002t0020 |
9 | HG00639.hp2 HG01243.hp1 HG01891.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*624_*634dupTGGGAG others(5): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 635 | INFO_REALIGN_3_PRIME | chr22 | 41906281 | |||||
| chr22:41906307 | G | A | 5 | a0001c0001t0002 a0002c0002t0002 a0002c0009t0002 others(2): Show |
54 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*647G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 647 | chr22 | 41906307 | ||||||
| chr22:41906322 | T | C | 1 | a0001c0001t0016 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 662 | chr22 | 41906322 | ||||||
| chr22:41906329 | A | G | 3 | a0001c0001t0007 a0002c0002t0007 a0002c0005t0005 |
10 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*669A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 669 | chr22 | 41906329 | ||||||
| chr22:41906460 | A | G | 11 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0013 others(8): Show |
30 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*800A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 800 | chr22 | 41906460 | ||||||
| chr22:41906520 | C | T | 1 | a0001c0001t0018 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*860C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 860 | chr22 | 41906520 | ||||||
| chr22:41906660 | G | A | 7 | a0001c0001t0003 a0001c0001t0012 a0001c0007t0003 others(4): Show |
39 | HG00738.hp1 HG00741.hp2 HG01106.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1000G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1000 | chr22 | 41906660 | ||||||
| chr22:41906851 | C | T | 1 | a0001c0001t0017 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1191C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1191 | chr22 | 41906851 | ||||||
| chr22:41906906 | G | A | 11 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0013 others(8): Show |
30 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1246G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1246 | chr22 | 41906906 | ||||||
| chr22:41906954 | G | C | 1 | a0004c0004t0010 | 2 | HG02257.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1294G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1294 | chr22 | 41906954 | ||||||
| chr22:41907016 | G | A | 1 | a0003c0010t0021 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1356G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1356 | chr22 | 41907016 | ||||||
| chr22:41907140 | G | A | 1 | a0001c0001t0011 | 2 | HG01943.hp2 HG02155.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1480G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1480 | chr22 | 41907140 | ||||||
| chr22:41907196 | G | A | 1 | a0004c0004t0009 | 3 | HG02559.hp2 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1536G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1536 | chr22 | 41907196 | ||||||
| chr22:41907246 | TTCAA | T | 9 | a0001c0001t0006 a0001c0001t0013 a0002c0002t0005 others(6): Show |
26 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1594_*1597delATCA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1594 | INFO_REALIGN_3_PRIME | chr22 | 41907246 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41833378 | G | T | 1 | a0002c0002t0003g0330 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.88+20G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41833378 | |||||||
| chr22:41833387 | G | A | 1 | a0004c0004t0003g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.88+29G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41833387 | |||||||
| chr22:41833531 | C | G | 6 | a0002c0002t0003g0325 a0002c0002t0003g0326 a0002c0002t0003g0327 others(3): Show |
6 | HG02630.hp1 HG02886.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+173C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41833531 | |||||||
| chr22:41833558 | C | T | 75 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(72): Show |
75 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.88+200C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41833558 | |||||||
| chr22:41833594 | G | T | 7 | a0002c0005t0005g0243 a0002c0005t0005g0244 a0002c0005t0005g0245 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+236G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41833594 | |||||||
| chr22:41833625 | A | G | 1 | a0001c0001t0004g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88+267A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41833625 | |||||||
| chr22:41833635 | C | T | 1 | a0001c0001t0002g0324 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.88+277C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41833635 | |||||||
| chr22:41834128 | C | T | 2 | a0001c0001t0007g0240 a0001c0001t0007g0241 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.88+770C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834128 | |||||||
| chr22:41834173 | G | A | 1 | a0001c0001t0001g0008 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.88+815G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834173 | |||||||
| chr22:41834345 | TCA | T | 202 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0001c0001t0001g0250 others(199): Show |
204 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.88+990_88+991delCA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41834345 | ||||||
| chr22:41834351 | C | T | 6 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(3): Show |
6 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+993C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834351 | |||||||
| chr22:41834468 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.88+1110G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834468 | |||||||
| chr22:41834477 | T | G | 1 | a0003c0003t0004g0117 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.88+1119T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834477 | |||||||
| chr22:41834584 | G | A | 1 | a0002c0002t0005g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88+1226G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834584 | |||||||
| chr22:41834678 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.88+1320C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834678 | |||||||
| chr22:41834708 | A | G | 1 | a0002c0002t0002g0112 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.88+1350A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834708 | |||||||
| chr22:41834776 | T | G | 1 | a0001c0007t0003g0010 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.88+1418T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834776 | |||||||
| chr22:41834931 | G | C | 1 | a0002c0002t0003g0011 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.88+1573G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834931 | |||||||
| chr22:41835230 | T | C | 250 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(247): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.88+1872T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835230 | |||||||
| chr22:41835231 | A | AGCTCACT others(128): Show |
250 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(247): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.88+1875_88+1876ins others(135): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41835231 | ||||||
| chr22:41835260 | C | G | 1 | a0001c0001t0001g0322 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.88+1902C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835260 | |||||||
| chr22:41835309 | A | AT | 20 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(17): Show |
20 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.88+1969dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41835309 | ||||||
| chr22:41835309 | AT | A | 48 | a0001c0001t0001g0006 a0001c0001t0001g0162 a0001c0001t0001g0163 others(45): Show |
49 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.88+1969delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41835309 | ||||||
| chr22:41835372 | G | A | 19 | a0001c0001t0003g0013 a0001c0001t0006g0021 a0002c0002t0006g0017 others(16): Show |
19 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.88+2014G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835372 | |||||||
| chr22:41835387 | C | G | 1 | a0002c0002t0002g0160 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.88+2029C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835387 | |||||||
| chr22:41835552 | C | T | 3 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0003c0003t0004g0106 |
3 | HG00597.hp2 HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.88+2194C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835552 | |||||||
| chr22:41835553 | G | A | 1 | a0002c0009t0002g0205 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.88+2195G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835553 | |||||||
| chr22:41835597 | A | C | 4 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(1): Show |
4 | HG00673.hp2 NA18971.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+2239A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835597 | |||||||
| chr22:41835602 | ACCTGGCC others(11): Show |
A | 1 | a0001c0001t0001g0320 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.88+2260_88+2277del others(18): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41835602 | ||||||
| chr22:41835875 | T | C | 2 | a0003c0010t0021g0025 a0008c0014t0005g0026 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.88+2517T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835875 | |||||||
| chr22:41835902 | G | A | 1 | a0002c0002t0003g0011 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.88+2544G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835902 | |||||||
| chr22:41836083 | T | C | 5 | a0002c0002t0002g0028 a0002c0002t0002g0030 a0002c0002t0002g0031 others(2): Show |
5 | HG00738.hp1 HG01106.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+2725T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41836083 | |||||||
| chr22:41836287 | G | A | 250 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(247): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.88+2929G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41836287 | |||||||
| chr22:41836480 | A | T | 4 | a0002c0002t0008g0317 a0002c0002t0008g0318 a0002c0002t0008g0319 others(1): Show |
4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+3122A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41836480 | |||||||
| chr22:41836573 | C | T | 59 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0001c0007t0003g0010 others(56): Show |
60 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.88+3215C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41836573 | |||||||
| chr22:41836584 | G | A | 60 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0002c0002t0001g0003 others(57): Show |
63 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.88+3226G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41836584 | |||||||
| chr22:41836784 | G | C | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.88+3426G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41836784 | |||||||
| chr22:41837035 | A | G | 2 | a0001c0001t0001g0315 a0001c0001t0014g0316 |
2 | HG00639.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.88+3677A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837035 | |||||||
| chr22:41837037 | G | T | 1 | a0002c0002t0002g0105 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.88+3679G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837037 | |||||||
| chr22:41837046 | C | T | 18 | a0001c0001t0001g0099 a0002c0002t0002g0012 a0002c0002t0002g0028 others(15): Show |
18 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.88+3688C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837046 | |||||||
| chr22:41837276 | G | C | 1 | a0008c0014t0005g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.88+3918G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837276 | |||||||
| chr22:41837367 | A | G | 1 | a0002c0002t0001g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.88+4009A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837367 | |||||||
| chr22:41837552 | T | C | 251 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(248): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.88+4194T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837552 | |||||||
| chr22:41837556 | T | TA | 41 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(38): Show |
41 | HG00423.hp1 HG00423.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+4218dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41837556 | ||||||
| chr22:41837556 | TA | T | 16 | a0001c0001t0001g0252 a0002c0002t0003g0001 a0002c0002t0003g0011 others(13): Show |
17 | HG02280.hp2 HG02630.hp1 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.88+4218delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41837556 | ||||||
| chr22:41837591 | G | T | 26 | a0001c0001t0003g0013 a0001c0001t0004g0242 a0001c0001t0006g0021 others(23): Show |
26 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.88+4233G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837591 | |||||||
| chr22:41837719 | G | A | 2 | a0001c0001t0001g0008 a0002c0002t0001g0121 |
2 | NA18951.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.88+4361G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837719 | |||||||
| chr22:41837858 | C | CA | 6 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG00733.hp1 HG01258.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+4517dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41837858 | ||||||
| chr22:41837858 | CA | C | 76 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(73): Show |
76 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.88+4517delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41837858 | ||||||
| chr22:41837872 | A | G | 2 | a0002c0002t0002g0091 a0002c0002t0002g0092 |
2 | HG00280.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.88+4514A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837872 | |||||||
| chr22:41837935 | A | G | 3 | a0004c0004t0003g0007 a0004c0004t0010g0046 a0004c0004t0010g0054 |
3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.88+4577A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837935 | |||||||
| chr22:41837951 | G | A | 54 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0002c0002t0001g0107 others(51): Show |
55 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.88+4593G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837951 | |||||||
| chr22:41838433 | T | A | 1 | a0001c0001t0003g0013 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.88+5075T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838433 | |||||||
| chr22:41838465 | GC | G | 6 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 others(3): Show |
6 | HG01106.hp1 HG01358.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+5108delC | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838465 | |||||||
| chr22:41838483 | A | G | 2 | a0004c0004t0001g0045 a0004c0004t0001g0053 |
2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.88+5125A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838483 | |||||||
| chr22:41838607 | C | T | 1 | a0001c0001t0004g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88+5249C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838607 | |||||||
| chr22:41838625 | T | C | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.88+5267T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838625 | |||||||
| chr22:41838637 | G | A | 2 | a0002c0002t0003g0325 a0002c0002t0003g0330 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.88+5279G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838637 | |||||||
| chr22:41838659 | G | C | 12 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(9): Show |
12 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.88+5301G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838659 | |||||||
| chr22:41838933 | C | T | 189 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0001c0001t0001g0250 others(186): Show |
191 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.88+5575C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838933 | |||||||
| chr22:41839015 | C | T | 1 | a0008c0014t0005g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.88+5657C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839015 | |||||||
| chr22:41839067 | G | A | 1 | a0002c0002t0001g0122 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.88+5709G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839067 | |||||||
| chr22:41839143 | A | T | 3 | a0004c0004t0003g0007 a0004c0004t0010g0046 a0004c0004t0010g0054 |
3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.88+5785A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839143 | |||||||
| chr22:41839148 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.88+5790G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839148 | |||||||
| chr22:41839215 | C | G | 61 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0001c0001t0001g0159 others(58): Show |
64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.88+5857C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839215 | |||||||
| chr22:41839247 | A | G | 1 | a0002c0002t0001g0005 | 2 | NA18961.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.88+5889A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839247 | |||||||
| chr22:41839300 | A | G | 1 | a0002c0005t0015g0248 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.88+5942A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839300 | |||||||
| chr22:41839348 | C | T | 98 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(95): Show |
99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.88+5990C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839348 | |||||||
| chr22:41839424 | G | A | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.88+6066G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839424 | |||||||
| chr22:41839454 | G | A | 1 | a0001c0001t0004g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88+6096G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839454 | |||||||
| chr22:41839583 | G | A | 2 | a0003c0010t0021g0025 a0008c0014t0005g0026 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.88+6225G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839583 | |||||||
| chr22:41839588 | C | T | 2 | a0002c0002t0003g0325 a0002c0002t0003g0330 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.88+6230C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839588 | |||||||
| chr22:41839651 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.88+6293C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839651 | |||||||
| chr22:41839746 | C | T | 4 | a0001c0001t0001g0008 a0002c0002t0001g0121 a0002c0002t0001g0157 others(1): Show |
4 | NA18951.hp2 NA18967.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+6388C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839746 | |||||||
| chr22:41839811 | T | C | 55 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0002c0002t0001g0107 others(52): Show |
56 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.88+6453T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839811 | |||||||
| chr22:41839814 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.88+6456A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839814 | |||||||
| chr22:41839956 | C | CT | 26 | a0001c0001t0001g0167 a0001c0001t0001g0239 a0001c0001t0001g0253 others(23): Show |
26 | HG00621.hp1 HG00639.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.88+6619dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41839956 | ||||||
| chr22:41839956 | CT | C | 26 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0007g0113 others(23): Show |
26 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.88+6619delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41839956 | ||||||
| chr22:41839956 | CTT | C | 66 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0001c0001t0001g0159 others(63): Show |
69 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.88+6618_88+6619del others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41839956 | ||||||
| chr22:41840087 | T | C | 1 | a0002c0002t0005g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.88+6729T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41840087 | |||||||
| chr22:41840100 | A | G | 2 | a0002c0002t0005g0009 a0002c0002t0005g0051 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.88+6742A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41840100 | |||||||
| chr22:41840149 | G | A | 61 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0001c0001t0001g0159 others(58): Show |
64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.88+6791G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41840149 | |||||||
| chr22:41840189 | T | A | 250 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(247): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.88+6831T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41840189 | |||||||
| chr22:41840333 | G | A | 250 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(247): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.88+6975G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41840333 | |||||||
| chr22:41840438 | CTCT | C | 80 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0001c0001t0003g0013 others(77): Show |
81 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.88+7085_88+7087del others(3): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41840438 | ||||||
| chr22:41840643 | C | T | 1 | a0001c0001t0003g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.88+7285C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41840643 | |||||||
| chr22:41840788 | A | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0301 |
2 | NA18962.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.88+7430A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41840788 | |||||||
| chr22:41841006 | C | T | 1 | a0005c0006t0004g0238 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.88+7648C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841006 | |||||||
| chr22:41841063 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.88+7705C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841063 | |||||||
| chr22:41841130 | G | C | 1 | a0001c0001t0003g0207 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.88+7772G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841130 | |||||||
| chr22:41841271 | T | G | 1 | a0002c0002t0008g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.88+7913T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841271 | |||||||
| chr22:41841396 | T | G | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.88+8038T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841396 | |||||||
| chr22:41841561 | C | T | 250 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(247): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.88+8203C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841561 | |||||||
| chr22:41841594 | G | T | 1 | a0005c0006t0004g0238 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.88+8236G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841594 | |||||||
| chr22:41841668 | ACTC | A | 3 | a0001c0001t0001g0162 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | NA18978.hp1 NA18986.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.88+8314_88+8316del others(3): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41841668 | ||||||
| chr22:41841765 | C | T | 250 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(247): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.88+8407C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841765 | |||||||
| chr22:41842023 | A | C | 61 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0001c0001t0001g0159 others(58): Show |
64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.88+8665A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842023 | |||||||
| chr22:41842138 | A | T | 1 | a0001c0001t0001g0300 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.88+8780A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842138 | |||||||
| chr22:41842236 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.88+8878G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842236 | |||||||
| chr22:41842715 | C | G | 2 | a0001c0001t0001g0199 a0010c0023t0001g0200 |
2 | NA18967.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.88+9357C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842715 | |||||||
| chr22:41842749 | G | A | 1 | a0001c0007t0003g0087 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.88+9391G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842749 | |||||||
| chr22:41842760 | C | T | 4 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 others(1): Show |
4 | HG01106.hp1 HG01517.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+9402C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842760 | |||||||
| chr22:41842905 | G | A | 6 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(3): Show |
6 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+9547G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842905 | |||||||
| chr22:41842986 | G | A | 2 | a0002c0005t0005g0015 a0002c0005t0005g0016 |
2 | HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.88+9628G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842986 | |||||||
| chr22:41842987 | T | A | 1 | a0005c0006t0004g0238 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.88+9629T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842987 | |||||||
| chr22:41842990 | C | CA | 10 | a0001c0001t0001g0172 a0002c0002t0002g0050 a0002c0002t0002g0109 others(7): Show |
10 | HG01243.hp2 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.88+9646dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41842990 | ||||||
| chr22:41842990 | CA | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0314 a0002c0002t0001g0003 others(10): Show |
15 | HG01517.hp2 NA18951.hp2 NA18965.hp2 others(12): Show |
intron_variant | MODIFIER | c.88+9646delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41842990 | ||||||
| chr22:41843218 | C | T | 18 | a0002c0002t0003g0001 a0002c0002t0003g0011 a0002c0002t0003g0058 others(15): Show |
19 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.88+9860C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41843218 | |||||||
| chr22:41843344 | G | C | 67 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0002c0002t0001g0003 others(64): Show |
70 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.88+9986G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41843344 | |||||||
| chr22:41843530 | G | A | 3 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 |
3 | HG01934.hp1 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.88+10172G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41843530 | |||||||
| chr22:41843536 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0302 |
2 | NA18988.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.88+10178G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41843536 | |||||||
| chr22:41843641 | AAGTTGCA others(6): Show |
A | 1 | a0001c0001t0001g0267 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.88+10286_88+10298d others(15): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41843641 | ||||||
| chr22:41843823 | C | T | 55 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0002c0002t0001g0107 others(52): Show |
56 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.88+10465C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41843823 | |||||||
| chr22:41843934 | T | C | 82 | a0001c0001t0001g0159 a0001c0001t0001g0250 a0001c0001t0001g0251 others(79): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.88+10576T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41843934 | |||||||
| chr22:41844015 | C | CA | 56 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0001c0001t0001g0162 others(53): Show |
59 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.88+10670dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844015 | ||||||
| chr22:41844027 | A | AAATACAC others(4): Show |
1 | a0002c0002t0002g0149 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.88+10670_88+10671i others(13): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844027 | ||||||
| chr22:41844027 | A | AAATACAC others(8): Show |
1 | a0002c0002t0002g0148 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.88+10670_88+10671i others(17): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844027 | ||||||
| chr22:41844029 | T | C | 2 | a0002c0002t0002g0148 a0002c0002t0002g0149 |
2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.88+10671T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844029 | |||||||
| chr22:41844029 | T | TACACAC | 5 | a0001c0001t0007g0113 a0002c0002t0002g0105 a0006c0008t0003g0114 others(2): Show |
5 | HG01346.hp1 HG02109.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+10674_88+10675i others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844029 | ||||||
| chr22:41844029 | TACATACA others(3): Show |
T | 1 | a0002c0002t0003g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.88+10675_88+10684d others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844029 | ||||||
| chr22:41844029 | TACATACA others(5): Show |
T | 1 | a0002c0002t0003g0056 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.88+10675_88+10686d others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844029 | ||||||
| chr22:41844033 | T | C | 69 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0001c0001t0007g0113 others(66): Show |
72 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.88+10675T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844033 | |||||||
| chr22:41844033 | T | TAC | 62 | a0001c0001t0001g0006 a0001c0001t0001g0162 a0001c0001t0001g0163 others(59): Show |
63 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.88+10706_88+10707d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | ||||||
| chr22:41844033 | T | TACAC | 4 | a0001c0001t0001g0202 a0001c0001t0001g0233 a0002c0002t0002g0062 others(1): Show |
4 | HG00673.hp2 HG03490.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+10704_88+10707d others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | ||||||
| chr22:41844033 | T | TACACAC | 32 | a0001c0001t0001g0069 a0002c0002t0001g0107 a0002c0002t0001g0108 others(29): Show |
33 | HG00597.hp2 HG00621.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.88+10702_88+10707d others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | ||||||
| chr22:41844033 | T | TACACACA others(1): Show |
17 | a0001c0001t0001g0099 a0001c0001t0001g0267 a0001c0001t0001g0269 others(14): Show |
17 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.88+10700_88+10707d others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | ||||||
| chr22:41844033 | T | TACACACA others(3): Show |
52 | a0001c0001t0001g0159 a0001c0001t0001g0251 a0001c0001t0001g0252 others(49): Show |
52 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.88+10698_88+10707d others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | ||||||
| chr22:41844033 | T | TACACACA others(5): Show |
20 | a0001c0001t0001g0250 a0001c0001t0001g0253 a0001c0001t0001g0261 others(17): Show |
20 | HG00733.hp2 HG01069.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.88+10696_88+10707d others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | ||||||
| chr22:41844033 | T | TACACACA others(7): Show |
1 | a0002c0002t0008g0319 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.88+10694_88+10707d others(16): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | ||||||
| chr22:41844033 | TACACACA others(11): Show |
T | 1 | a0002c0016t0002g0077 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.88+10690_88+10707d others(20): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | ||||||
| chr22:41844048 | A | ACACACAC others(3): Show |
2 | a0001c0001t0001g0313 a0001c0001t0001g0314 |
2 | HG01106.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.88+10699_88+10700i others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844048 | ||||||
| chr22:41844065 | C | CACACACA others(7): Show |
5 | a0002c0002t0002g0118 a0002c0002t0002g0150 a0003c0003t0004g0124 others(2): Show |
5 | HG00642.hp2 HG03831.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+10707_88+10708i others(16): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844065 | |||||||
| chr22:41844065 | C | CACACACA others(5): Show |
4 | a0002c0002t0001g0151 a0002c0002t0003g0326 a0002c0002t0003g0327 others(1): Show |
4 | HG03942.hp1 NA19003.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+10707_88+10708i others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844065 | |||||||
| chr22:41844065 | C | CACACACA others(3): Show |
27 | a0001c0001t0001g0128 a0002c0002t0001g0003 a0002c0002t0001g0004 others(24): Show |
30 | HG00099.hp1 HG01169.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.88+10707_88+10708i others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844065 | |||||||
| chr22:41844065 | C | CACACACA others(1): Show |
47 | a0001c0001t0001g0008 a0001c0001t0003g0013 a0001c0001t0006g0021 others(44): Show |
48 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.88+10707_88+10708i others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844065 | |||||||
| chr22:41844065 | C | CACACAT | 9 | a0002c0002t0001g0042 a0002c0002t0001g0043 a0002c0002t0001g0122 others(6): Show |
9 | HG01934.hp1 HG01943.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+10707_88+10708i others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844065 | |||||||
| chr22:41844065 | C | CACAT | 5 | a0002c0002t0001g0040 a0002c0002t0001g0147 a0002c0002t0002g0039 others(2): Show |
5 | HG01109.hp1 HG01243.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+10707_88+10708i others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844065 | |||||||
| chr22:41844065 | C | T | 5 | a0002c0002t0003g0055 a0002c0002t0003g0056 a0002c0005t0005g0015 others(2): Show |
5 | HG02486.hp1 HG02886.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+10707C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844065 | |||||||
| chr22:41844340 | G | T | 1 | a0002c0005t0005g0244 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.88+10982G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844340 | |||||||
| chr22:41844429 | C | T | 1 | a0002c0005t0005g0243 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.88+11071C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844429 | |||||||
| chr22:41844614 | C | T | 1 | a0002c0002t0001g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.88+11256C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844614 | |||||||
| chr22:41844625 | G | A | 3 | a0004c0004t0003g0007 a0004c0004t0010g0046 a0004c0004t0010g0054 |
3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.88+11267G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844625 | |||||||
| chr22:41844672 | G | C | 3 | a0004c0004t0003g0007 a0004c0004t0010g0046 a0004c0004t0010g0054 |
3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.88+11314G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844672 | |||||||
| chr22:41844793 | C | T | 250 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(247): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.88+11435C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844793 | |||||||
| chr22:41844903 | G | C | 1 | a0004c0004t0005g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.88+11545G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844903 | |||||||
| chr22:41845158 | T | G | 1 | a0002c0002t0002g0160 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.88+11800T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41845158 | |||||||
| chr22:41845198 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.88+11840C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41845198 | |||||||
| chr22:41845368 | G | A | 64 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0002c0002t0001g0003 others(61): Show |
67 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.88+12010G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41845368 | |||||||
| chr22:41845391 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.88+12033G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41845391 | |||||||
| chr22:41845454 | T | A | 1 | a0005c0006t0004g0238 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.88+12096T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41845454 | |||||||
| chr22:41845779 | T | A | 1 | a0001c0001t0001g0268 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.88+12421T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41845779 | |||||||
| chr22:41846031 | T | A | 6 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(3): Show |
6 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+12673T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41846031 | |||||||
| chr22:41846053 | G | T | 12 | a0001c0001t0003g0013 a0001c0001t0006g0021 a0002c0002t0006g0017 others(9): Show |
12 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.88+12695G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41846053 | |||||||
| chr22:41846494 | C | T | 1 | a0002c0002t0002g0031 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.88+13136C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41846494 | |||||||
| chr22:41847016 | T | C | 251 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(248): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.88+13658T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847016 | |||||||
| chr22:41847517 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.88+14159G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847517 | |||||||
| chr22:41847578 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.88+14220G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847578 | |||||||
| chr22:41847614 | T | C | 77 | a0001c0001t0001g0159 a0001c0001t0001g0250 a0001c0001t0001g0251 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.88+14256T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847614 | |||||||
| chr22:41847837 | T | C | 100 | a0001c0001t0001g0159 a0001c0001t0001g0250 a0001c0001t0001g0251 others(97): Show |
101 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.88+14479T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847837 | |||||||
| chr22:41847838 | A | T | 3 | a0001c0001t0003g0305 a0001c0001t0003g0306 a0001c0001t0003g0307 |
3 | HG01433.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.88+14480A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847838 | |||||||
| chr22:41847917 | A | AT | 19 | a0001c0001t0006g0021 a0002c0002t0002g0080 a0002c0002t0002g0081 others(16): Show |
19 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.88+14561dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41847917 | ||||||
| chr22:41847920 | A | AT | 158 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0001c0001t0001g0159 others(155): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.88+14575dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41847920 | ||||||
| chr22:41847920 | A | T | 22 | a0001c0001t0001g0198 a0001c0001t0001g0213 a0001c0001t0003g0013 others(19): Show |
22 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.88+14562A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847920 | |||||||
| chr22:41847922 | T | TA | 70 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0001c0001t0001g0270 others(67): Show |
72 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.88+14564_88+14565i others(3): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847922 | |||||||
| chr22:41847925 | T | A | 5 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(2): Show |
5 | HG01934.hp1 HG01943.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+14567T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847925 | |||||||
| chr22:41848030 | C | G | 21 | a0001c0001t0003g0305 a0001c0001t0003g0306 a0001c0001t0003g0307 others(18): Show |
22 | HG01433.hp1 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.88+14672C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41848030 | |||||||
| chr22:41848137 | C | T | 1 | a0002c0005t0005g0245 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88+14779C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41848137 | |||||||
| chr22:41848190 | C | T | 1 | a0002c0002t0006g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.88+14832C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41848190 | |||||||
| chr22:41848208 | G | A | 55 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0002c0002t0001g0107 others(52): Show |
56 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.88+14850G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41848208 | |||||||
| chr22:41848379 | G | A | 13 | a0001c0001t0001g0069 a0002c0002t0001g0107 a0002c0002t0001g0108 others(10): Show |
14 | HG00597.hp2 HG00621.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.88+15021G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41848379 | |||||||
| chr22:41848548 | C | T | 1 | a0002c0002t0002g0084 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.88+15190C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41848548 | |||||||
| chr22:41848841 | G | T | 2 | a0002c0002t0001g0145 a0003c0003t0004g0136 |
2 | HG00099.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.88+15483G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41848841 | |||||||
| chr22:41849269 | G | C | 1 | a0002c0002t0001g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.88+15911G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849269 | |||||||
| chr22:41849510 | C | G | 5 | a0001c0007t0003g0010 a0001c0007t0003g0087 a0001c0007t0003g0088 others(2): Show |
5 | HG01934.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+16152C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849510 | |||||||
| chr22:41849718 | G | T | 59 | a0001c0001t0001g0008 a0002c0002t0001g0003 a0002c0002t0001g0004 others(56): Show |
62 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.88+16360G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849718 | |||||||
| chr22:41849759 | C | T | 249 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(246): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.88+16401C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849759 | |||||||
| chr22:41849863 | G | T | 1 | a0001c0001t0006g0021 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.88+16505G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849863 | |||||||
| chr22:41849940 | C | CATCAGGA others(1): Show |
142 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(139): Show |
146 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.88+16585_88+16586i others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41849940 | ||||||
| chr22:41849944 | C | G | 142 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(139): Show |
146 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.88+16586C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849944 | |||||||
| chr22:41849945 | T | A | 142 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(139): Show |
146 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.88+16587T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849945 | |||||||
| chr22:41849962 | C | A | 6 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(3): Show |
6 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+16604C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849962 | |||||||
| chr22:41849966 | A | G | 249 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(246): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.88+16608A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849966 | |||||||
| chr22:41850033 | G | A | 55 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0002c0002t0001g0107 others(52): Show |
56 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.88+16675G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850033 | |||||||
| chr22:41850046 | G | A | 1 | a0002c0002t0005g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88+16688G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850046 | |||||||
| chr22:41850091 | G | T | 12 | a0001c0001t0003g0013 a0001c0001t0006g0021 a0002c0002t0006g0017 others(9): Show |
12 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.88+16733G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850091 | |||||||
| chr22:41850307 | G | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | NA18950.hp2 NA18982.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.89-16524G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850307 | |||||||
| chr22:41850388 | C | T | 249 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0099 others(246): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.89-16443C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850388 | |||||||
| chr22:41850449 | C | CA | 63 | a0001c0001t0001g0008 a0001c0001t0001g0162 a0001c0001t0001g0227 others(60): Show |
66 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.89-16367dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41850449 | ||||||
| chr22:41850503 | C | T | 7 | a0002c0002t0002g0050 a0002c0002t0002g0109 a0004c0004t0001g0045 others(4): Show |
7 | HG02559.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-16328C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850503 | |||||||
| chr22:41850560 | T | A | 25 | a0002c0002t0002g0050 a0002c0002t0002g0109 a0002c0002t0003g0001 others(22): Show |
26 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.89-16271T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850560 | |||||||
| chr22:41850665 | C | A | 1 | a0002c0002t0005g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-16166C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850665 | |||||||
| chr22:41850750 | CTTTTTG | C | 82 | a0001c0001t0001g0159 a0001c0001t0001g0250 a0001c0001t0001g0251 others(79): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.89-16075_89-16070d others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41850750 | ||||||
| chr22:41851144 | A | G | 2 | a0001c0001t0001g0194 a0001c0001t0016g0195 |
2 | HG00597.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.89-15687A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851144 | |||||||
| chr22:41851356 | G | A | 79 | a0001c0001t0001g0159 a0001c0001t0001g0250 a0001c0001t0001g0251 others(76): Show |
79 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.89-15475G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851356 | |||||||
| chr22:41851379 | A | G | 5 | a0002c0002t0002g0050 a0002c0002t0002g0109 a0004c0004t0009g0047 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-15452A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851379 | |||||||
| chr22:41851487 | TTTTG | T | 5 | a0001c0001t0001g0165 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | HG00423.hp1 HG00558.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-15328_89-15325d others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41851487 | ||||||
| chr22:41851499 | G | GT | 59 | a0001c0001t0001g0008 a0002c0002t0001g0003 a0002c0002t0001g0004 others(56): Show |
62 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.89-15329dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41851499 | ||||||
| chr22:41851503 | G | GT | 24 | a0001c0001t0003g0013 a0001c0001t0004g0242 a0001c0001t0006g0021 others(21): Show |
24 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.89-15321dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41851503 | ||||||
| chr22:41851503 | G | T | 71 | a0001c0001t0001g0008 a0002c0002t0001g0003 a0002c0002t0001g0004 others(68): Show |
74 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.89-15328G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851503 | |||||||
| chr22:41851605 | T | C | 1 | a0001c0001t0001g0271 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.89-15226T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851605 | |||||||
| chr22:41851691 | C | T | 78 | a0001c0001t0001g0159 a0001c0001t0001g0250 a0001c0001t0001g0251 others(75): Show |
78 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.89-15140C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851691 | |||||||
| chr22:41851762 | T | G | 1 | a0001c0001t0003g0013 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.89-15069T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851762 | |||||||
| chr22:41851800 | G | A | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-15031G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851800 | |||||||
| chr22:41851823 | A | C | 1 | a0002c0002t0002g0072 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.89-15008A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851823 | |||||||
| chr22:41851928 | G | A | 236 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0128 others(233): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.89-14903G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851928 | |||||||
| chr22:41851948 | G | A | 6 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(3): Show |
6 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-14883G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851948 | |||||||
| chr22:41851980 | G | A | 10 | a0001c0001t0001g0099 a0001c0001t0001g0272 a0002c0002t0002g0012 others(7): Show |
10 | HG00323.hp2 HG01069.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-14851G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851980 | |||||||
| chr22:41852086 | A | G | 3 | a0002c0002t0008g0317 a0002c0002t0008g0318 a0002c0002t0008g0321 |
3 | HG01109.hp2 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.89-14745A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852086 | |||||||
| chr22:41852126 | A | G | 3 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | HG01081.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.89-14705A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852126 | |||||||
| chr22:41852177 | G | A | 27 | a0002c0002t0002g0050 a0002c0002t0002g0109 a0002c0002t0003g0001 others(24): Show |
28 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.89-14654G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852177 | |||||||
| chr22:41852278 | A | G | 14 | a0002c0002t0003g0001 a0002c0002t0003g0011 a0002c0002t0003g0058 others(11): Show |
15 | HG01884.hp1 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.89-14553A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852278 | |||||||
| chr22:41852285 | C | T | 2 | a0001c0001t0001g0315 a0001c0001t0014g0316 |
2 | HG00639.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.89-14546C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852285 | |||||||
| chr22:41852351 | T | A | 1 | a0002c0002t0001g0158 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.89-14480T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852351 | |||||||
| chr22:41852354 | A | T | 1 | a0002c0002t0001g0158 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.89-14477A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852354 | |||||||
| chr22:41852359 | A | C | 1 | a0002c0002t0001g0158 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.89-14472A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852359 | |||||||
| chr22:41852368 | A | T | 1 | a0002c0002t0001g0158 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.89-14463A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852368 | |||||||
| chr22:41852520 | G | A | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-14311G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852520 | |||||||
| chr22:41852728 | A | AT | 36 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0002g0012 others(33): Show |
36 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.89-14072dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | ||||||
| chr22:41852728 | A | ATT | 21 | a0001c0001t0001g0099 a0002c0002t0002g0030 a0002c0002t0002g0063 others(18): Show |
21 | HG00323.hp2 HG00735.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.89-14073_89-14072d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | ||||||
| chr22:41852728 | AT | A | 67 | a0001c0001t0001g0162 a0001c0001t0001g0166 a0001c0001t0001g0167 others(64): Show |
68 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.89-14072delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | ||||||
| chr22:41852728 | ATT | A | 83 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0128 others(80): Show |
86 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.89-14073_89-14072d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | ||||||
| chr22:41852728 | ATTT | A | 53 | a0001c0001t0001g0069 a0001c0001t0001g0159 a0001c0001t0001g0177 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.89-14074_89-14072d others(5): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | ||||||
| chr22:41852728 | ATTTTTTT others(1): Show |
A | 6 | a0002c0002t0001g0033 a0002c0002t0001g0034 a0002c0002t0002g0050 others(3): Show |
6 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-14079_89-14072d others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | ||||||
| chr22:41852728 | ATTTTTTT others(2): Show |
A | 31 | a0002c0002t0001g0032 a0002c0002t0001g0035 a0002c0002t0001g0036 others(28): Show |
32 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.89-14080_89-14072d others(11): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | ||||||
| chr22:41852728 | ATTTTTTT others(3): Show |
A | 1 | a0004c0004t0010g0046 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.89-14081_89-14072d others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | ||||||
| chr22:41852728 | ATTTTTTT others(10): Show |
A | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-14088_89-14072d others(19): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | ||||||
| chr22:41852817 | A | G | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-14014A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852817 | |||||||
| chr22:41852856 | G | A | 253 | a0001c0001t0001g0159 a0001c0001t0001g0227 a0001c0001t0001g0235 others(250): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.89-13975G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852856 | |||||||
| chr22:41852889 | G | T | 1 | a0001c0001t0001g0290 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.89-13942G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852889 | |||||||
| chr22:41852911 | A | G | 1 | a0002c0002t0003g0327 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.89-13920A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852911 | |||||||
| chr22:41852969 | C | T | 3 | a0004c0004t0003g0007 a0004c0004t0010g0046 a0004c0004t0010g0054 |
3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.89-13862C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852969 | |||||||
| chr22:41853493 | A | G | 1 | a0001c0012t0001g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.89-13338A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41853493 | |||||||
| chr22:41853525 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.89-13306A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41853525 | |||||||
| chr22:41853603 | GT | G | 3 | a0004c0004t0003g0007 a0004c0004t0010g0046 a0004c0004t0010g0054 |
3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.89-13227delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41853603 | |||||||
| chr22:41853927 | C | T | 38 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(35): Show |
39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-12904C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41853927 | |||||||
| chr22:41853939 | G | A | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-12892G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41853939 | |||||||
| chr22:41853951 | C | T | 4 | a0002c0002t0008g0317 a0002c0002t0008g0318 a0002c0002t0008g0319 others(1): Show |
4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-12880C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41853951 | |||||||
| chr22:41853991 | C | T | 30 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(27): Show |
31 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.89-12840C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41853991 | |||||||
| chr22:41854021 | C | T | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-12810C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854021 | |||||||
| chr22:41854130 | TTTG | T | 60 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0002g0002 others(57): Show |
61 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.89-12689_89-12687d others(5): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41854130 | ||||||
| chr22:41854288 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.89-12543A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854288 | |||||||
| chr22:41854395 | C | G | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-12436C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854395 | |||||||
| chr22:41854503 | C | T | 2 | a0002c0002t0003g0027 a0002c0002t0003g0029 |
2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.89-12328C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854503 | |||||||
| chr22:41854565 | C | CT | 38 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(35): Show |
39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-12263dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41854565 | ||||||
| chr22:41854726 | G | A | 1 | a0004c0004t0003g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.89-12105G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854726 | |||||||
| chr22:41854794 | G | T | 2 | a0001c0001t0011g0175 a0001c0001t0019g0176 |
2 | HG02155.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.89-12037G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854794 | |||||||
| chr22:41854798 | G | T | 2 | a0001c0001t0011g0175 a0001c0001t0019g0176 |
2 | HG02155.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.89-12033G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854798 | |||||||
| chr22:41854802 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0001c0001t0001g0202 others(2): Show |
5 | HG00673.hp2 NA18953.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-12029G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854802 | |||||||
| chr22:41854894 | A | G | 5 | a0002c0002t0003g0001 a0002c0002t0003g0011 a0002c0002t0003g0058 others(2): Show |
6 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-11937A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854894 | |||||||
| chr22:41854988 | G | A | 2 | a0001c0012t0001g0309 a0001c0012t0001g0310 |
2 | HG01358.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.89-11843G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854988 | |||||||
| chr22:41854999 | C | T | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-11832C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854999 | |||||||
| chr22:41855019 | T | TA | 7 | a0001c0001t0001g0181 a0001c0001t0001g0260 a0001c0001t0001g0261 others(4): Show |
7 | HG01109.hp1 HG01496.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-11796dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41855019 | ||||||
| chr22:41855019 | T | TAA | 51 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0002g0002 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.89-11797_89-11796d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41855019 | ||||||
| chr22:41855019 | TA | T | 7 | a0002c0002t0003g0055 a0002c0002t0003g0056 a0002c0005t0005g0243 others(4): Show |
7 | HG02451.hp1 HG02486.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-11796delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41855019 | ||||||
| chr22:41855032 | A | C | 1 | a0004c0004t0003g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.89-11799A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855032 | |||||||
| chr22:41855049 | A | C | 38 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(35): Show |
39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-11782A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855049 | |||||||
| chr22:41855064 | T | G | 1 | a0002c0002t0006g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.89-11767T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855064 | |||||||
| chr22:41855119 | T | C | 56 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0002g0002 others(53): Show |
57 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.89-11712T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855119 | |||||||
| chr22:41855186 | T | A | 48 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(45): Show |
51 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.89-11645T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855186 | |||||||
| chr22:41855397 | G | A | 1 | a0004c0004t0010g0046 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.89-11434G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855397 | |||||||
| chr22:41855432 | G | A | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-11399G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855432 | |||||||
| chr22:41855521 | C | CA | 5 | a0001c0001t0001g0232 a0001c0001t0001g0271 a0001c0001t0003g0207 others(2): Show |
5 | HG00140.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-11302dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41855521 | ||||||
| chr22:41855754 | A | C | 3 | a0001c0001t0003g0305 a0001c0001t0003g0306 a0001c0001t0003g0307 |
3 | HG01433.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.89-11077A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855754 | |||||||
| chr22:41855755 | C | CT | 10 | a0001c0001t0001g0188 a0001c0001t0002g0256 a0002c0002t0001g0032 others(7): Show |
10 | HG00423.hp2 HG00733.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-11059dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41855755 | ||||||
| chr22:41855755 | CT | C | 68 | a0001c0001t0001g0206 a0001c0001t0001g0228 a0001c0001t0001g0235 others(65): Show |
69 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.89-11059delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41855755 | ||||||
| chr22:41855806 | G | T | 82 | a0001c0001t0001g0159 a0001c0001t0001g0227 a0001c0001t0001g0235 others(79): Show |
82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.89-11025G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855806 | |||||||
| chr22:41855909 | C | T | 1 | a0002c0002t0002g0086 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.89-10922C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855909 | |||||||
| chr22:41855913 | G | C | 12 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(9): Show |
12 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.89-10918G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855913 | |||||||
| chr22:41855957 | A | G | 2 | a0002c0009t0002g0205 a0002c0009t0002g0223 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.89-10874A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855957 | |||||||
| chr22:41856090 | G | GT | 6 | a0002c0002t0003g0325 a0002c0002t0003g0326 a0002c0002t0003g0327 others(3): Show |
6 | HG02630.hp1 HG02886.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-10732dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41856090 | ||||||
| chr22:41856176 | G | A | 38 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(35): Show |
39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-10655G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856176 | |||||||
| chr22:41856212 | C | T | 1 | a0002c0002t0001g0131 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.89-10619C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856212 | |||||||
| chr22:41856223 | C | T | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-10608C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856223 | |||||||
| chr22:41856252 | G | A | 1 | a0002c0005t0005g0247 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-10579G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856252 | |||||||
| chr22:41856413 | G | A | 4 | a0005c0006t0004g0120 a0005c0006t0004g0126 a0005c0006t0004g0134 others(1): Show |
4 | NA18942.hp1 NA18978.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-10418G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856413 | |||||||
| chr22:41856585 | C | G | 45 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(42): Show |
48 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.89-10246C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856585 | |||||||
| chr22:41856803 | G | A | 1 | a0002c0002t0002g0074 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.89-10028G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856803 | |||||||
| chr22:41856823 | C | G | 2 | a0002c0002t0002g0073 a0002c0002t0002g0105 |
2 | HG01167.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.89-10008C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856823 | |||||||
| chr22:41856890 | C | G | 60 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0002g0002 others(57): Show |
61 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.89-9941C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856890 | |||||||
| chr22:41856956 | A | G | 60 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0002g0002 others(57): Show |
61 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.89-9875A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856956 | |||||||
| chr22:41856958 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.89-9873A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856958 | |||||||
| chr22:41856971 | A | T | 2 | a0001c0001t0001g0290 a0001c0001t0001g0297 |
2 | NA18979.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.89-9860A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856971 | |||||||
| chr22:41857021 | C | T | 1 | a0002c0002t0001g0144 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.89-9810C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857021 | |||||||
| chr22:41857042 | G | A | 1 | a0003c0003t0004g0132 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.89-9789G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857042 | |||||||
| chr22:41857066 | C | CA | 70 | a0001c0001t0001g0186 a0001c0001t0001g0250 a0001c0001t0001g0270 others(67): Show |
73 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.89-9749dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41857066 | ||||||
| chr22:41857066 | C | CAA | 79 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(76): Show |
80 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.89-9750_89-9749dup others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41857066 | ||||||
| chr22:41857447 | G | A | 1 | a0004c0004t0001g0224 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.89-9384G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857447 | |||||||
| chr22:41857585 | G | A | 3 | a0001c0001t0001g0206 a0001c0001t0001g0213 a0001c0001t0011g0210 |
3 | HG01517.hp1 HG01943.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.89-9246G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857585 | |||||||
| chr22:41857708 | C | T | 1 | a0002c0002t0003g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.89-9123C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857708 | |||||||
| chr22:41857723 | G | A | 45 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(42): Show |
48 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.89-9108G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857723 | |||||||
| chr22:41857759 | C | T | 45 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(42): Show |
48 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.89-9072C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857759 | |||||||
| chr22:41857823 | T | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0225 |
2 | HG00673.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.89-9008T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857823 | |||||||
| chr22:41858048 | G | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0180 |
2 | NA18952.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.89-8783G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858048 | |||||||
| chr22:41858086 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0012g0215 |
2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.89-8745G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858086 | |||||||
| chr22:41858121 | C | T | 1 | a0002c0002t0001g0121 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.89-8710C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858121 | |||||||
| chr22:41858196 | G | C | 1 | a0001c0001t0001g0159 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.89-8635G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858196 | |||||||
| chr22:41858355 | A | G | 3 | a0005c0006t0004g0120 a0005c0006t0004g0134 a0005c0006t0004g0135 |
3 | NA18978.hp2 NA19004.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.89-8476A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858355 | |||||||
| chr22:41858517 | A | AGG | 38 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(35): Show |
39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-8313_89-8312dup others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41858517 | ||||||
| chr22:41858812 | T | C | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-8019T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858812 | |||||||
| chr22:41858846 | A | T | 2 | a0003c0003t0004g0124 a0003c0003t0004g0125 |
2 | NA18939.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.89-7985A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858846 | |||||||
| chr22:41858914 | C | T | 1 | a0002c0002t0002g0105 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.89-7917C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858914 | |||||||
| chr22:41858926 | G | A | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-7905G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858926 | |||||||
| chr22:41858984 | G | T | 5 | a0001c0007t0003g0010 a0001c0007t0003g0087 a0001c0007t0003g0088 others(2): Show |
5 | HG01934.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-7847G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858984 | |||||||
| chr22:41859145 | G | A | 1 | a0003c0003t0004g0138 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.89-7686G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859145 | |||||||
| chr22:41859371 | A | T | 1 | a0001c0001t0001g0296 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.89-7460A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859371 | |||||||
| chr22:41859521 | A | G | 246 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(243): Show |
252 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.89-7310A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859521 | |||||||
| chr22:41859701 | A | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(45): Show |
51 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.89-7130A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859701 | |||||||
| chr22:41859709 | G | C | 1 | a0002c0002t0005g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-7122G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859709 | |||||||
| chr22:41859799 | C | CT | 94 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0001t0001g0099 others(91): Show |
95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.89-7003dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41859799 | ||||||
| chr22:41859799 | C | CTT | 37 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0001c0001t0001g0164 others(34): Show |
37 | HG00558.hp1 HG00733.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.89-7004_89-7003dup others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41859799 | ||||||
| chr22:41859799 | CT | C | 36 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0121 others(33): Show |
38 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.89-7003delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41859799 | ||||||
| chr22:41859799 | CTT | C | 16 | a0002c0002t0001g0033 a0002c0002t0001g0034 a0002c0002t0001g0043 others(13): Show |
16 | HG01943.hp1 HG02559.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-7004_89-7003del others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41859799 | ||||||
| chr22:41859799 | CTTT | C | 27 | a0002c0002t0001g0032 a0002c0002t0001g0035 a0002c0002t0001g0036 others(24): Show |
28 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.89-7005_89-7003del others(3): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41859799 | ||||||
| chr22:41859799 | CTTTTTTT others(6): Show |
C | 1 | a0002c0002t0002g0105 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.89-7015_89-7003del others(13): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41859799 | ||||||
| chr22:41859941 | G | A | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-6890G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859941 | |||||||
| chr22:41859963 | G | A | 1 | a0002c0002t0008g0319 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.89-6868G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859963 | |||||||
| chr22:41859988 | G | A | 6 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(3): Show |
6 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-6843G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859988 | |||||||
| chr22:41860052 | G | A | 3 | a0001c0001t0003g0305 a0001c0001t0003g0306 a0001c0001t0003g0307 |
3 | HG01433.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.89-6779G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41860052 | |||||||
| chr22:41860084 | T | C | 318 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(315): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.89-6747T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41860084 | |||||||
| chr22:41860207 | G | A | 1 | a0008c0014t0005g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.89-6624G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41860207 | |||||||
| chr22:41860241 | GA | G | 40 | a0001c0001t0001g0228 a0001c0001t0012g0215 a0002c0002t0001g0032 others(37): Show |
41 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.89-6577delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41860241 | ||||||
| chr22:41860431 | T | C | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-6400T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41860431 | |||||||
| chr22:41860520 | A | T | 1 | a0002c0002t0002g0031 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.89-6311A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41860520 | |||||||
| chr22:41860535 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.89-6296A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41860535 | |||||||
| chr22:41860810 | C | T | 45 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(42): Show |
48 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.89-6021C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41860810 | |||||||
| chr22:41861017 | G | A | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-5814G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41861017 | |||||||
| chr22:41861206 | G | A | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-5625G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41861206 | |||||||
| chr22:41861259 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.89-5572G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41861259 | |||||||
| chr22:41861641 | G | A | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-5190G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41861641 | |||||||
| chr22:41861664 | T | G | 1 | a0001c0001t0001g0265 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.89-5167T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41861664 | |||||||
| chr22:41861689 | G | A | 38 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(35): Show |
39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-5142G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41861689 | |||||||
| chr22:41861790 | G | T | 1 | a0002c0002t0001g0042 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.89-5041G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41861790 | |||||||
| chr22:41862011 | C | T | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4820C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862011 | |||||||
| chr22:41862012 | C | A | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4819C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862012 | |||||||
| chr22:41862013 | C | T | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4818C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862013 | |||||||
| chr22:41862018 | C | G | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4813C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862018 | |||||||
| chr22:41862019 | C | T | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4812C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862019 | |||||||
| chr22:41862026 | G | GTATTTAA others(6): Show |
2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4805_89-4804ins others(13): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862026 | |||||||
| chr22:41862028 | C | G | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4803C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862028 | |||||||
| chr22:41862030 | G | A | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4801G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862030 | |||||||
| chr22:41862031 | G | T | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4800G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862031 | |||||||
| chr22:41862032 | G | T | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4799G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862032 | |||||||
| chr22:41862045 | G | A | 246 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(243): Show |
252 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.89-4786G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862045 | |||||||
| chr22:41862268 | G | A | 38 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(35): Show |
39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-4563G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862268 | |||||||
| chr22:41862333 | G | C | 1 | a0002c0002t0005g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-4498G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862333 | |||||||
| chr22:41862440 | G | A | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-4391G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862440 | |||||||
| chr22:41862442 | G | T | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-4389G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862442 | |||||||
| chr22:41862573 | C | G | 59 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0002g0002 others(56): Show |
60 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-4258C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862573 | |||||||
| chr22:41862655 | A | G | 2 | a0002c0002t0001g0122 a0002c0002t0001g0154 |
2 | NA18977.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.89-4176A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862655 | |||||||
| chr22:41862756 | G | A | 1 | a0002c0015t0002g0068 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.89-4075G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862756 | |||||||
| chr22:41862836 | C | T | 6 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(3): Show |
6 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-3995C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862836 | |||||||
| chr22:41863094 | C | T | 246 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(243): Show |
252 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.89-3737C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863094 | |||||||
| chr22:41863112 | G | A | 1 | a0002c0005t0005g0244 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.89-3719G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863112 | |||||||
| chr22:41863504 | A | G | 1 | a0003c0003t0004g0142 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.89-3327A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863504 | |||||||
| chr22:41863520 | C | G | 5 | a0002c0002t0001g0137 a0002c0002t0001g0143 a0002c0002t0001g0144 others(2): Show |
5 | HG00621.hp2 NA18747.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-3311C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863520 | |||||||
| chr22:41863520 | C | T | 6 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG00733.hp1 HG01258.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-3311C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863520 | |||||||
| chr22:41863648 | A | G | 5 | a0002c0002t0003g0001 a0002c0002t0003g0011 a0002c0002t0003g0058 others(2): Show |
6 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-3183A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863648 | |||||||
| chr22:41863680 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0225 |
2 | HG00673.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.89-3151G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863680 | |||||||
| chr22:41863860 | C | CATTT | 18 | a0002c0002t0006g0017 a0002c0002t0006g0018 a0002c0002t0006g0019 others(15): Show |
18 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.89-2960_89-2957dup others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41863860 | ||||||
| chr22:41863904 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.89-2927C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863904 | |||||||
| chr22:41863905 | G | A | 4 | a0005c0006t0004g0120 a0005c0006t0004g0126 a0005c0006t0004g0134 others(1): Show |
4 | NA18942.hp1 NA18978.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2926G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863905 | |||||||
| chr22:41864165 | C | T | 38 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(35): Show |
39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-2666C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864165 | |||||||
| chr22:41864223 | C | CAT | 42 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0162 others(39): Show |
43 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.89-2570_89-2569dup others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | ||||||
| chr22:41864223 | C | CATAT | 27 | a0001c0001t0001g0169 a0001c0001t0001g0250 a0001c0001t0001g0261 others(24): Show |
27 | HG00642.hp1 HG01175.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-2572_89-2569dup others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | ||||||
| chr22:41864223 | C | CATATAT | 32 | a0001c0001t0001g0128 a0001c0001t0001g0164 a0001c0001t0001g0172 others(29): Show |
32 | HG00099.hp2 HG00558.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.89-2574_89-2569dup others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | ||||||
| chr22:41864223 | C | CATATATA others(1): Show |
31 | a0001c0001t0001g0069 a0001c0001t0001g0188 a0001c0001t0001g0202 others(28): Show |
31 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.89-2576_89-2569dup others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | ||||||
| chr22:41864223 | C | CATATATA others(3): Show |
1 | a0005c0021t0001g0258 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.89-2578_89-2569dup others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | ||||||
| chr22:41864223 | C | CATATATA others(9): Show |
2 | a0002c0002t0002g0062 a0002c0002t0002g0075 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.89-2584_89-2569dup others(16): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | ||||||
| chr22:41864223 | C | CATATATA others(11): Show |
1 | a0001c0001t0001g0322 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.89-2586_89-2569dup others(18): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | ||||||
| chr22:41864223 | CAT | C | 8 | a0001c0001t0001g0252 a0001c0001t0001g0273 a0001c0001t0001g0302 others(5): Show |
8 | HG01106.hp1 HG02129.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-2570_89-2569del others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | ||||||
| chr22:41864223 | CATATATA others(3): Show |
C | 5 | a0001c0001t0001g0099 a0001c0001t0001g0228 a0001c0001t0001g0231 others(2): Show |
5 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-2578_89-2569del others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | ||||||
| chr22:41864223 | CATATATA others(5): Show |
C | 4 | a0001c0001t0001g0221 a0001c0001t0001g0230 a0001c0001t0001g0232 others(1): Show |
4 | HG00140.hp1 HG00735.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-2580_89-2569del others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | ||||||
| chr22:41864223 | CATATATA others(7): Show |
C | 5 | a0001c0001t0001g0229 a0001c0001t0007g0113 a0006c0008t0003g0114 others(2): Show |
5 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-2582_89-2569del others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | ||||||
| chr22:41864223 | CATATATA others(9): Show |
C | 2 | a0001c0001t0007g0240 a0001c0001t0007g0241 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.89-2584_89-2569del others(16): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | ||||||
| chr22:41864249 | TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.89-2580_89-2567del others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864249 | ||||||
| chr22:41864251 | TATATATA others(5): Show |
T | 4 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(1): Show |
4 | HG01258.hp1 HG01517.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-2578_89-2567del others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864251 | ||||||
| chr22:41864251 | TATATATA others(7): Show |
T | 1 | a0002c0002t0005g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-2578_89-2565del others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864251 | ||||||
| chr22:41864251 | TATATATA others(9): Show |
T | 1 | a0002c0002t0006g0023 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.89-2578_89-2563del others(16): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864251 | ||||||
| chr22:41864253 | TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.89-2576_89-2567del others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864253 | ||||||
| chr22:41864255 | T | C | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-2576T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864255 | |||||||
| chr22:41864255 | TATATATA others(1): Show |
T | 5 | a0002c0002t0002g0086 a0002c0002t0002g0160 a0002c0002t0003g0327 others(2): Show |
5 | HG03017.hp2 HG03225.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-2574_89-2567del others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864255 | ||||||
| chr22:41864255 | TATATATA others(3): Show |
T | 9 | a0002c0002t0001g0032 a0002c0002t0001g0034 a0002c0002t0001g0035 others(6): Show |
9 | HG00408.hp2 HG00423.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-2574_89-2565del others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864255 | ||||||
| chr22:41864255 | TATATATA others(5): Show |
T | 2 | a0002c0005t0005g0015 a0002c0005t0005g0246 |
2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.89-2574_89-2563del others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864255 | ||||||
| chr22:41864257 | T | C | 3 | a0002c0002t0003g0055 a0002c0002t0003g0056 a0003c0003t0004g0141 |
3 | HG02886.hp2 HG02897.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.89-2574T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864257 | |||||||
| chr22:41864257 | T | TACAC | 3 | a0002c0002t0001g0129 a0002c0002t0001g0157 a0003c0003t0004g0142 |
3 | HG03704.hp1 NA18959.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.89-2573_89-2572ins others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864257 | ||||||
| chr22:41864257 | T | TACACAC | 3 | a0002c0002t0001g0119 a0002c0002t0001g0139 a0002c0025t0001g0140 |
3 | NA18946.hp1 NA18979.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.89-2573_89-2572ins others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864257 | ||||||
| chr22:41864257 | TATATAC | T | 29 | a0002c0002t0001g0040 a0002c0002t0002g0028 a0002c0002t0002g0030 others(26): Show |
29 | HG00738.hp1 HG00741.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.89-2572_89-2567del others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864257 | ||||||
| chr22:41864257 | TATATACA others(1): Show |
T | 3 | a0002c0002t0001g0033 a0002c0002t0001g0036 a0002c0002t0005g0051 |
3 | HG00673.hp1 HG02559.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.89-2572_89-2565del others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864257 | ||||||
| chr22:41864257 | TATATACA others(3): Show |
T | 2 | a0002c0002t0006g0019 a0002c0005t0005g0016 |
2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.89-2572_89-2563del others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864257 | ||||||
| chr22:41864259 | T | C | 10 | a0002c0002t0001g0119 a0002c0002t0001g0129 a0002c0002t0001g0139 others(7): Show |
10 | HG02886.hp2 HG02897.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-2572T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864259 | |||||||
| chr22:41864259 | T | TACACAC | 17 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0121 others(14): Show |
17 | HG01169.hp2 HG01981.hp1 HG03017.hp1 others(14): Show |
intron_variant | MODIFIER | c.89-2571_89-2570ins others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864259 | ||||||
| chr22:41864259 | T | TACACACA others(3): Show |
1 | a0005c0006t0004g0134 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.89-2571_89-2570ins others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864259 | ||||||
| chr22:41864259 | TATAC | T | 18 | a0002c0002t0001g0108 a0002c0002t0002g0002 a0002c0002t0002g0012 others(15): Show |
19 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.89-2570_89-2567del others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864259 | ||||||
| chr22:41864259 | TATACAC | T | 3 | a0002c0002t0002g0094 a0002c0002t0002g0097 a0003c0003t0004g0096 |
3 | HG01257.hp1 HG01258.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.89-2570_89-2565del others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864259 | ||||||
| chr22:41864261 | T | C | 31 | a0001c0001t0001g0099 a0001c0001t0001g0159 a0002c0002t0001g0003 others(28): Show |
31 | HG00323.hp2 HG01169.hp2 HG01981.hp1 others(28): Show |
intron_variant | MODIFIER | c.89-2570T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864261 | |||||||
| chr22:41864261 | T | TACACACA others(1): Show |
5 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0133 others(2): Show |
6 | HG00099.hp1 NA18945.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-2554_89-2547dup others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | ||||||
| chr22:41864261 | T | TACACACA others(3): Show |
6 | a0002c0002t0001g0003 a0002c0002t0001g0144 a0003c0003t0004g0138 others(3): Show |
6 | HG00621.hp2 HG01081.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-2556_89-2547dup others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | ||||||
| chr22:41864261 | T | TATAC | 4 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0275 others(1): Show |
4 | HG02293.hp1 NA18942.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-2569_89-2568ins others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | ||||||
| chr22:41864261 | T | TATACACA others(3): Show |
5 | a0002c0002t0002g0118 a0002c0002t0002g0148 a0002c0002t0002g0150 others(2): Show |
5 | HG00642.hp2 HG03225.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-2569_89-2568ins others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | ||||||
| chr22:41864261 | T | TATACACA others(5): Show |
1 | a0002c0002t0001g0147 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.89-2569_89-2568ins others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | ||||||
| chr22:41864261 | T | TATATAC | 5 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0276 others(2): Show |
5 | HG00639.hp1 HG02451.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-2569_89-2568ins others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | ||||||
| chr22:41864261 | T | TATATACA others(5): Show |
2 | a0002c0002t0001g0131 a0002c0013t0001g0226 |
2 | HG02145.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.89-2569_89-2568ins others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | ||||||
| chr22:41864261 | T | TATATACA others(7): Show |
1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-2569_89-2568ins others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | ||||||
| chr22:41864261 | TAC | T | 13 | a0001c0001t0001g0177 a0002c0002t0002g0073 a0002c0002t0002g0095 others(10): Show |
13 | HG01167.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.89-2548_89-2547del others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | ||||||
| chr22:41864263 | C | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(78): Show |
82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.89-2568C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864263 | |||||||
| chr22:41864265 | C | T | 12 | a0001c0001t0001g0198 a0002c0002t0006g0017 a0002c0002t0006g0018 others(9): Show |
12 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.89-2566C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864265 | |||||||
| chr22:41864267 | C | T | 65 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0002g0002 others(62): Show |
66 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.89-2564C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864267 | |||||||
| chr22:41864269 | C | T | 3 | a0002c0002t0002g0094 a0002c0002t0002g0097 a0003c0003t0004g0096 |
3 | HG01257.hp1 HG01258.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.89-2562C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864269 | |||||||
| chr22:41864295 | ATATATAT others(7): Show |
A | 2 | a0002c0005t0005g0015 a0002c0005t0005g0246 |
2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.89-2522_89-2509del others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864295 | ||||||
| chr22:41864307 | A | G | 1 | a0002c0002t0002g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.89-2524A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864307 | |||||||
| chr22:41864309 | G | A | 1 | a0002c0002t0002g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.89-2522G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864309 | |||||||
| chr22:41864309 | G | GTA | 4 | a0001c0020t0001g0281 a0002c0002t0003g0326 a0002c0002t0008g0317 others(1): Show |
4 | HG00099.hp2 HG01109.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-2508_89-2507dup others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864309 | ||||||
| chr22:41864309 | G | GTATA | 4 | a0002c0002t0001g0032 a0004c0004t0003g0007 a0004c0004t0010g0046 others(1): Show |
4 | HG00423.hp2 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2510_89-2507dup others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864309 | ||||||
| chr22:41864322 | TA | T | 37 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(34): Show |
40 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.89-2508delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864322 | |||||||
| chr22:41864323 | A | ATAT | 5 | a0002c0002t0003g0001 a0002c0002t0003g0011 a0002c0002t0003g0058 others(2): Show |
6 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-2507_89-2506ins others(3): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864323 | ||||||
| chr22:41864323 | A | T | 44 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(41): Show |
45 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.89-2508A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864323 | |||||||
| chr22:41864323 | AT | A | 9 | a0002c0002t0001g0137 a0002c0002t0001g0143 a0002c0002t0001g0144 others(6): Show |
9 | HG00280.hp2 HG00621.hp2 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-2493delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864323 | ||||||
| chr22:41864324 | T | TA | 65 | a0001c0001t0001g0220 a0001c0001t0007g0113 a0001c0001t0007g0240 others(62): Show |
66 | HG00597.hp2 HG00621.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.89-2507_89-2506ins others(1): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864324 | |||||||
| chr22:41864324 | T | TATA | 24 | a0002c0002t0001g0033 a0002c0002t0001g0034 a0002c0002t0001g0035 others(21): Show |
24 | HG00408.hp2 HG00673.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.89-2507_89-2506ins others(3): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864324 | |||||||
| chr22:41864324 | T | TATATA | 3 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 |
3 | HG01934.hp1 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.89-2507_89-2506ins others(5): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864324 | |||||||
| chr22:41864325 | T | A | 40 | a0001c0001t0001g0228 a0001c0001t0001g0232 a0001c0001t0001g0233 others(37): Show |
40 | HG00140.hp1 HG00423.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.89-2506T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864325 | |||||||
| chr22:41864326 | T | A | 82 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(79): Show |
83 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.89-2505T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864326 | |||||||
| chr22:41864327 | T | A | 6 | a0002c0002t0001g0032 a0002c0002t0003g0326 a0003c0010t0021g0025 others(3): Show |
6 | HG00423.hp2 HG02257.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-2504T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864327 | |||||||
| chr22:41864328 | T | A | 1 | a0002c0002t0002g0063 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.89-2503T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864328 | |||||||
| chr22:41864329 | T | A | 1 | a0002c0002t0001g0032 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.89-2502T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864329 | |||||||
| chr22:41864333 | T | C | 1 | a0008c0014t0005g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.89-2498T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864333 | |||||||
| chr22:41864609 | C | T | 1 | a0004c0004t0009g0047 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.89-2222C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864609 | |||||||
| chr22:41864646 | G | C | 1 | a0002c0002t0012g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.89-2185G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864646 | |||||||
| chr22:41864967 | C | G | 59 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0002g0002 others(56): Show |
60 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-1864C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864967 | |||||||
| chr22:41865146 | A | C | 1 | a0001c0001t0001g0303 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.89-1685A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41865146 | |||||||
| chr22:41865146 | AAC | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(98): Show |
102 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.89-1663_89-1662del others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41865146 | ||||||
| chr22:41865146 | AACAC | A | 145 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(142): Show |
150 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.89-1665_89-1662del others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41865146 | ||||||
| chr22:41865327 | T | A | 1 | a0001c0001t0001g0271 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.89-1504T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41865327 | |||||||
| chr22:41865356 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0213 a0001c0001t0011g0210 |
3 | HG01517.hp1 HG01943.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.89-1475C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41865356 | |||||||
| chr22:41865968 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.89-863C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41865968 | |||||||
| chr22:41866037 | C | T | 1 | a0004c0004t0010g0054 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.89-794C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866037 | |||||||
| chr22:41866043 | G | A | 1 | a0003c0003t0004g0138 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.89-788G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866043 | |||||||
| chr22:41866116 | C | T | 3 | a0002c0002t0003g0325 a0002c0002t0003g0330 a0002c0002t0005g0009 |
3 | HG01884.hp1 HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.89-715C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866116 | |||||||
| chr22:41866209 | G | A | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-622G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866209 | |||||||
| chr22:41866325 | T | C | 12 | a0002c0002t0002g0050 a0002c0002t0002g0109 a0004c0004t0001g0045 others(9): Show |
12 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.89-506T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866325 | |||||||
| chr22:41866407 | G | A | 4 | a0002c0002t0002g0118 a0002c0002t0002g0148 a0002c0002t0002g0149 others(1): Show |
4 | HG00642.hp2 HG03831.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-424G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866407 | |||||||
| chr22:41866443 | A | G | 246 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(243): Show |
252 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.89-388A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866443 | |||||||
| chr22:41867663 | C | T | 1 | a0002c0002t0006g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.538+383C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/18 | chr22 | 41867663 | |||||||
| chr22:41867680 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.538+400G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/18 | chr22 | 41867680 | |||||||
| chr22:41867694 | C | A | 1 | a0002c0002t0002g0073 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.538+414C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/18 | chr22 | 41867694 | |||||||
| chr22:41867813 | G | GA | 37 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(34): Show |
38 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.538+544dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 41867813 | ||||||
| chr22:41868265 | G | T | 163 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(160): Show |
168 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.539-346G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/18 | chr22 | 41868265 | |||||||
| chr22:41868307 | G | A | 1 | a0002c0002t0003g0330 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.539-304G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/18 | chr22 | 41868307 | |||||||
| chr22:41869186 | C | T | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.720+394C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869186 | |||||||
| chr22:41869296 | G | GGTTTTAC others(1): Show |
158 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0172 others(155): Show |
163 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.720+504_720+505ins others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869296 | |||||||
| chr22:41869300 | T | C | 5 | a0002c0002t0003g0001 a0002c0002t0003g0011 a0002c0002t0003g0058 others(2): Show |
6 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+508T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869300 | |||||||
| chr22:41869327 | C | T | 1 | a0003c0003t0004g0117 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.720+535C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869327 | |||||||
| chr22:41869338 | C | T | 1 | a0002c0002t0006g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.720+546C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869338 | |||||||
| chr22:41869373 | C | T | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.720+581C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869373 | |||||||
| chr22:41869426 | G | A | 48 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(45): Show |
51 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.720+634G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869426 | |||||||
| chr22:41869464 | G | T | 1 | a0001c0001t0001g0300 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.720+672G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869464 | |||||||
| chr22:41869489 | A | AT | 10 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0001t0001g0163 others(7): Show |
11 | HG00544.hp2 HG00597.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.720+709dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 41869489 | ||||||
| chr22:41869501 | TG | T | 163 | a0001c0001t0001g0186 a0002c0002t0001g0003 a0002c0002t0001g0004 others(160): Show |
168 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.720+711delG | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 41869501 | ||||||
| chr22:41869502 | G | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(78): Show |
82 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.720+710G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869502 | |||||||
| chr22:41869529 | G | C | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.720+737G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869529 | |||||||
| chr22:41869596 | G | A | 4 | a0002c0005t0005g0015 a0002c0005t0005g0245 a0002c0005t0005g0247 others(1): Show |
4 | HG02486.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+804G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869596 | |||||||
| chr22:41869597 | C | A | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.720+805C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869597 | |||||||
| chr22:41869609 | A | G | 1 | a0003c0017t0004g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.720+817A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869609 | |||||||
| chr22:41869677 | G | A | 3 | a0006c0008t0003g0114 a0006c0008t0003g0115 a0006c0008t0003g0116 |
3 | HG02109.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.720+885G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869677 | |||||||
| chr22:41869862 | CT | C | 30 | a0001c0001t0001g0199 a0002c0002t0001g0032 a0002c0002t0001g0033 others(27): Show |
31 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.721-1014delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 41869862 | ||||||
| chr22:41869916 | C | T | 19 | a0002c0002t0005g0051 a0002c0002t0006g0017 a0002c0002t0006g0018 others(16): Show |
19 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.721-973C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869916 | |||||||
| chr22:41870164 | T | G | 51 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(48): Show |
54 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.721-725T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41870164 | |||||||
| chr22:41870415 | A | G | 246 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(243): Show |
252 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.721-474A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41870415 | |||||||
| chr22:41870628 | C | CA | 33 | a0001c0001t0001g0188 a0001c0001t0001g0199 a0001c0001t0001g0239 others(30): Show |
34 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.721-238dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 41870628 | ||||||
| chr22:41870628 | C | CAA | 10 | a0002c0002t0001g0034 a0002c0002t0001g0035 a0002c0002t0001g0037 others(7): Show |
10 | HG01934.hp1 HG02004.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.721-239_721-238dup others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 41870628 | ||||||
| chr22:41870628 | CA | C | 168 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(165): Show |
173 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.721-238delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 41870628 | ||||||
| chr22:41871192 | C | T | 29 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(26): Show |
30 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.867+157C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871192 | |||||||
| chr22:41871347 | C | G | 1 | a0002c0002t0006g0024 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.867+312C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871347 | |||||||
| chr22:41871601 | C | A | 244 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(241): Show |
250 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.867+566C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871601 | |||||||
| chr22:41871619 | C | T | 30 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(27): Show |
31 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.867+584C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871619 | |||||||
| chr22:41871700 | T | A | 1 | a0002c0002t0002g0105 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.867+665T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871700 | |||||||
| chr22:41871788 | A | C | 1 | a0002c0002t0002g0063 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.867+753A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871788 | |||||||
| chr22:41871796 | G | A | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.867+761G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871796 | |||||||
| chr22:41871898 | C | CA | 86 | a0001c0001t0001g0199 a0001c0001t0001g0262 a0001c0001t0001g0268 others(83): Show |
90 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.867+879dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 41871898 | ||||||
| chr22:41871898 | C | CAA | 62 | a0002c0002t0001g0037 a0002c0002t0001g0107 a0002c0002t0001g0108 others(59): Show |
63 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.867+878_867+879dup others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 41871898 | ||||||
| chr22:41871976 | C | T | 11 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0119 others(8): Show |
13 | NA18951.hp2 NA18965.hp2 NA18967.hp2 others(10): Show |
intron_variant | MODIFIER | c.867+941C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871976 | |||||||
| chr22:41872024 | G | A | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.867+989G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41872024 | |||||||
| chr22:41872106 | C | T | 18 | a0002c0002t0006g0017 a0002c0002t0006g0018 a0002c0002t0006g0019 others(15): Show |
18 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.867+1071C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41872106 | |||||||
| chr22:41872225 | G | A | 1 | a0002c0005t0005g0246 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.867+1190G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41872225 | |||||||
| chr22:41872245 | G | A | 30 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(27): Show |
31 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.867+1210G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41872245 | |||||||
| chr22:41872249 | CA | C | 144 | a0001c0001t0001g0225 a0002c0002t0001g0003 a0002c0002t0001g0004 others(141): Show |
149 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.867+1229delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 41872249 | ||||||
| chr22:41872677 | G | A | 2 | a0002c0002t0001g0107 a0002c0002t0001g0108 |
2 | HG00597.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.868-1121G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41872677 | |||||||
| chr22:41872717 | C | T | 60 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0002g0002 others(57): Show |
61 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.868-1081C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41872717 | |||||||
| chr22:41872892 | C | CA | 7 | a0001c0001t0001g0191 a0001c0001t0003g0207 a0002c0002t0003g0001 others(4): Show |
8 | HG00558.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.868-895dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 41872892 | ||||||
| chr22:41873124 | G | A | 30 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(27): Show |
31 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.868-674G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873124 | |||||||
| chr22:41873184 | C | T | 1 | a0002c0002t0002g0063 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.868-614C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873184 | |||||||
| chr22:41873370 | T | G | 8 | a0002c0002t0002g0050 a0002c0002t0002g0079 a0002c0002t0002g0080 others(5): Show |
8 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.868-428T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873370 | |||||||
| chr22:41873449 | G | A | 1 | a0002c0002t0002g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.868-349G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873449 | |||||||
| chr22:41873467 | C | G | 1 | a0001c0001t0018g0193 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.868-331C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873467 | |||||||
| chr22:41873525 | A | G | 1 | a0001c0001t0018g0193 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.868-273A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873525 | |||||||
| chr22:41873528 | C | T | 11 | a0001c0001t0001g0227 a0001c0001t0001g0235 a0001c0001t0001g0236 others(8): Show |
11 | HG00280.hp1 HG00639.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.868-270C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873528 | |||||||
| chr22:41873559 | T | C | 2 | a0002c0002t0005g0009 a0002c0002t0005g0051 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.868-239T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873559 | |||||||
| chr22:41873624 | C | T | 75 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(72): Show |
76 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.868-174C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873624 | |||||||
| chr22:41873721 | C | T | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.868-77C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873721 | |||||||
| chr22:41873727 | G | T | 3 | a0004c0004t0003g0007 a0004c0004t0010g0046 a0004c0004t0010g0054 |
3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.868-71G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873727 | |||||||
| chr22:41873763 | G | A | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.868-35G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873763 | |||||||
| chr22:41874084 | G | T | 1 | a0004c0004t0001g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1089+65G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874084 | |||||||
| chr22:41874230 | G | C | 2 | a0002c0002t0002g0050 a0002c0002t0002g0109 |
2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1089+211G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874230 | |||||||
| chr22:41874319 | C | G | 1 | a0001c0001t0001g0323 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1089+300C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874319 | |||||||
| chr22:41874645 | C | T | 5 | a0002c0002t0003g0001 a0002c0002t0003g0011 a0002c0002t0003g0058 others(2): Show |
6 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089+626C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874645 | |||||||
| chr22:41874703 | C | A | 60 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0002g0002 others(57): Show |
61 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1090-634C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874703 | |||||||
| chr22:41874813 | A | C | 2 | a0002c0002t0002g0095 a0009c0019t0001g0098 |
2 | HG03942.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1090-524A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874813 | |||||||
| chr22:41874840 | G | A | 54 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(51): Show |
57 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1090-497G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874840 | |||||||
| chr22:41874860 | T | C | 12 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(9): Show |
12 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1090-477T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874860 | |||||||
| chr22:41874870 | G | C | 2 | a0002c0002t0002g0095 a0009c0019t0001g0098 |
2 | HG03942.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1090-467G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874870 | |||||||
| chr22:41874931 | A | G | 1 | a0002c0002t0002g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1090-406A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874931 | |||||||
| chr22:41875026 | A | C | 3 | a0004c0004t0003g0007 a0004c0004t0010g0046 a0004c0004t0010g0054 |
3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1090-311A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41875026 | |||||||
| chr22:41875050 | G | A | 5 | a0001c0001t0001g0252 a0001c0001t0001g0283 a0001c0001t0001g0285 others(2): Show |
5 | NA18973.hp1 NA18988.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-287G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41875050 | |||||||
| chr22:41875117 | C | A | 1 | a0002c0002t0006g0024 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1090-220C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41875117 | |||||||
| chr22:41875263 | G | A | 1 | a0001c0012t0001g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1090-74G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41875263 | |||||||
| chr22:41875289 | T | C | 7 | a0002c0002t0002g0050 a0002c0002t0002g0080 a0002c0002t0002g0081 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1090-48T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41875289 | |||||||
| chr22:41875756 | A | G | 2 | a0004c0004t0001g0045 a0004c0004t0001g0053 |
2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1386+32A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41875756 | |||||||
| chr22:41875838 | A | G | 2 | a0004c0004t0010g0046 a0004c0004t0010g0054 |
2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1386+114A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41875838 | |||||||
| chr22:41875951 | G | A | 3 | a0004c0004t0003g0007 a0004c0004t0010g0046 a0004c0004t0010g0054 |
3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1386+227G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41875951 | |||||||
| chr22:41876031 | C | A | 2 | a0002c0002t0003g0055 a0002c0002t0003g0056 |
2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1386+307C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876031 | |||||||
| chr22:41876211 | A | T | 8 | a0002c0002t0006g0017 a0002c0002t0006g0018 a0002c0002t0006g0019 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+487A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876211 | |||||||
| chr22:41876266 | G | A | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1386+542G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876266 | |||||||
| chr22:41876342 | G | A | 2 | a0002c0009t0002g0205 a0002c0009t0002g0223 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1386+618G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876342 | |||||||
| chr22:41876389 | G | A | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1386+665G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876389 | |||||||
| chr22:41876538 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1387-691A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876538 | |||||||
| chr22:41876588 | A | C | 1 | a0002c0002t0006g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1387-641A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876588 | |||||||
| chr22:41876829 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1387-400C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876829 | |||||||
| chr22:41877089 | G | C | 1 | a0002c0002t0002g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1387-140G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41877089 | |||||||
| chr22:41877458 | G | A | 30 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(27): Show |
31 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1579+37G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 8/18 | chr22 | 41877458 | |||||||
| chr22:41877510 | C | T | 1 | a0002c0002t0001g0043 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1579+89C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 8/18 | chr22 | 41877510 | |||||||
| chr22:41877724 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1580-218A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 8/18 | chr22 | 41877724 | |||||||
| chr22:41877838 | A | G | 18 | a0002c0002t0006g0017 a0002c0002t0006g0018 a0002c0002t0006g0019 others(15): Show |
18 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1580-104A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 8/18 | chr22 | 41877838 | |||||||
| chr22:41877929 | C | T | 3 | a0002c0002t0003g0066 a0002c0002t0003g0078 a0002c0002t0003g0110 |
3 | HG01243.hp2 HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1580-13C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 8/18 | chr22 | 41877929 | |||||||
| chr22:41878283 | G | A | 60 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0002g0002 others(57): Show |
61 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1761+160G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41878283 | |||||||
| chr22:41878398 | G | A | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1761+275G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41878398 | |||||||
| chr22:41878553 | G | A | 1 | a0002c0002t0007g0329 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1761+430G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41878553 | |||||||
| chr22:41878877 | G | A | 1 | a0002c0002t0002g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1761+754G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41878877 | |||||||
| chr22:41879081 | G | T | 1 | a0002c0002t0005g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1761+958G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41879081 | |||||||
| chr22:41879411 | A | G | 31 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(28): Show |
32 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1761+1288A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41879411 | |||||||
| chr22:41879472 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1762-1244G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41879472 | |||||||
| chr22:41879504 | G | C | 2 | a0002c0005t0005g0016 a0002c0005t0005g0246 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1762-1212G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41879504 | |||||||
| chr22:41879566 | G | A | 2 | a0002c0002t0003g0078 a0002c0002t0003g0110 |
2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1762-1150G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41879566 | |||||||
| chr22:41879705 | C | T | 3 | a0002c0002t0003g0066 a0002c0002t0003g0078 a0002c0002t0003g0110 |
3 | HG01243.hp2 HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1762-1011C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41879705 | |||||||
| chr22:41879975 | A | T | 4 | a0002c0005t0005g0015 a0002c0005t0005g0245 a0002c0005t0005g0247 others(1): Show |
4 | HG02486.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1762-741A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41879975 | |||||||
| chr22:41880274 | G | A | 1 | a0001c0001t0003g0013 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1762-442G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41880274 | |||||||
| chr22:41880284 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0011g0210 |
2 | HG01943.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1762-432G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41880284 | |||||||
| chr22:41880287 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0011g0210 |
2 | HG01943.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1762-429C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41880287 | |||||||
| chr22:41880383 | C | G | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1762-333C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41880383 | |||||||
| chr22:41880397 | C | CA | 102 | a0001c0001t0001g0099 a0001c0001t0001g0185 a0001c0001t0001g0188 others(99): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1762-300dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr22 | 41880397 | ||||||
| chr22:41880397 | C | CAA | 6 | a0001c0001t0003g0207 a0002c0002t0002g0111 a0002c0002t0008g0317 others(3): Show |
6 | HG01109.hp2 HG01175.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1762-301_1762-300d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr22 | 41880397 | ||||||
| chr22:41880452 | C | T | 3 | a0004c0004t0009g0047 a0004c0004t0009g0048 a0004c0004t0009g0049 |
3 | HG02559.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1762-264C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41880452 | |||||||
| chr22:41880578 | G | C | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1762-138G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41880578 | |||||||
| chr22:41881115 | G | A | 1 | a0002c0002t0002g0086 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2038+123G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41881115 | |||||||
| chr22:41881713 | G | T | 1 | a0002c0016t0002g0077 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2038+721G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41881713 | |||||||
| chr22:41881788 | C | A | 47 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0002g0002 others(44): Show |
48 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.2038+796C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41881788 | |||||||
| chr22:41881882 | G | A | 1 | a0002c0005t0015g0248 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2038+890G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41881882 | |||||||
| chr22:41881901 | A | G | 1 | a0001c0011t0001g0259 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2038+909A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41881901 | |||||||
| chr22:41882215 | T | C | 1 | a0002c0002t0001g0131 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2038+1223T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41882215 | |||||||
| chr22:41882241 | A | G | 31 | a0001c0001t0001g0187 a0002c0002t0001g0032 a0002c0002t0001g0033 others(28): Show |
32 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.2038+1249A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41882241 | |||||||
| chr22:41882320 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2038+1328G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41882320 | |||||||
| chr22:41882562 | T | C | 60 | a0001c0001t0001g0172 a0002c0002t0001g0003 a0002c0002t0001g0004 others(57): Show |
63 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.2038+1570T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41882562 | |||||||
| chr22:41882571 | C | G | 1 | a0008c0014t0005g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2038+1579C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41882571 | |||||||
| chr22:41882953 | A | G | 8 | a0002c0002t0006g0017 a0002c0002t0006g0018 a0002c0002t0006g0019 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2039-1889A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41882953 | |||||||
| chr22:41883054 | C | T | 1 | a0002c0002t0003g0326 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2039-1788C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41883054 | |||||||
| chr22:41883331 | C | T | 2 | a0002c0002t0003g0325 a0002c0002t0003g0330 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2039-1511C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41883331 | |||||||
| chr22:41883397 | G | A | 16 | a0002c0002t0002g0050 a0002c0002t0002g0080 a0002c0002t0002g0081 others(13): Show |
16 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.2039-1445G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41883397 | |||||||
| chr22:41883502 | G | C | 75 | a0001c0001t0001g0274 a0001c0001t0003g0305 a0001c0001t0003g0306 others(72): Show |
76 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.2039-1340G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41883502 | |||||||
| chr22:41883567 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2039-1275C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41883567 | |||||||
| chr22:41883649 | A | G | 43 | a0001c0001t0001g0099 a0001c0001t0001g0206 a0001c0001t0001g0211 others(40): Show |
44 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.2039-1193A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41883649 | |||||||
| chr22:41883886 | G | A | 1 | a0001c0001t0013g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2039-956G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41883886 | |||||||
| chr22:41884010 | G | C | 3 | a0002c0002t0001g0131 a0003c0003t0004g0124 a0003c0003t0004g0125 |
3 | NA18939.hp1 NA18969.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2039-832G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884010 | |||||||
| chr22:41884060 | T | TG | 147 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(144): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.2039-781dupG | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr22 | 41884060 | ||||||
| chr22:41884130 | C | CA | 9 | a0001c0001t0001g0185 a0002c0002t0006g0017 a0002c0002t0006g0018 others(6): Show |
9 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2039-712_2039-711i others(3): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884130 | |||||||
| chr22:41884131 | G | A | 118 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(115): Show |
122 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.2039-711G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884131 | |||||||
| chr22:41884133 | G | T | 9 | a0001c0001t0001g0185 a0002c0002t0006g0017 a0002c0002t0006g0018 others(6): Show |
9 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2039-709G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884133 | |||||||
| chr22:41884134 | T | G | 1 | a0002c0002t0002g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2039-708T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884134 | |||||||
| chr22:41884226 | C | T | 1 | a0002c0002t0006g0018 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2039-616C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884226 | |||||||
| chr22:41884357 | G | A | 191 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(188): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2039-485G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884357 | |||||||
| chr22:41884383 | G | A | 1 | a0002c0015t0002g0068 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2039-459G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884383 | |||||||
| chr22:41884614 | T | C | 109 | a0001c0001t0001g0263 a0001c0001t0001g0286 a0002c0002t0001g0003 others(106): Show |
113 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.2039-228T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884614 | |||||||
| chr22:41884769 | G | A | 1 | a0007c0026t0001g0304 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2039-73G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884769 | |||||||
| chr22:41885145 | T | G | 34 | a0001c0001t0001g0263 a0001c0001t0001g0286 a0002c0002t0001g0032 others(31): Show |
35 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2208+134T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885145 | |||||||
| chr22:41885151 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2208+140G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885151 | |||||||
| chr22:41885251 | C | A | 33 | a0001c0001t0001g0263 a0001c0001t0001g0286 a0002c0002t0001g0032 others(30): Show |
34 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.2208+240C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885251 | |||||||
| chr22:41885256 | G | T | 1 | a0002c0002t0002g0084 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2208+245G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885256 | |||||||
| chr22:41885290 | A | G | 33 | a0001c0001t0001g0263 a0001c0001t0001g0286 a0002c0002t0001g0032 others(30): Show |
34 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.2208+279A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885290 | |||||||
| chr22:41885425 | A | G | 254 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(251): Show |
260 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2208+414A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885425 | |||||||
| chr22:41885557 | C | T | 4 | a0002c0002t0008g0317 a0002c0002t0008g0318 a0002c0002t0008g0319 others(1): Show |
4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2208+546C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885557 | |||||||
| chr22:41885583 | C | T | 33 | a0001c0001t0001g0263 a0001c0001t0001g0286 a0002c0002t0001g0032 others(30): Show |
34 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.2208+572C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885583 | |||||||
| chr22:41886008 | C | T | 60 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(57): Show |
63 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2208+997C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41886008 | |||||||
| chr22:41886254 | A | G | 1 | a0001c0001t0004g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2208+1243A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41886254 | |||||||
| chr22:41886263 | C | G | 3 | a0001c0001t0003g0305 a0001c0001t0003g0306 a0001c0001t0003g0307 |
3 | HG01433.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2208+1252C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41886263 | |||||||
| chr22:41886755 | C | T | 8 | a0002c0002t0006g0017 a0002c0002t0006g0018 a0002c0002t0006g0019 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2208+1744C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41886755 | |||||||
| chr22:41886812 | T | A | 1 | a0001c0001t0013g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2208+1801T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41886812 | |||||||
| chr22:41886939 | C | CA | 4 | a0002c0002t0002g0063 a0002c0002t0003g0027 a0002c0002t0003g0029 others(1): Show |
4 | HG00738.hp1 HG00741.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.2208+1929dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41886939 | ||||||
| chr22:41887010 | G | A | 1 | a0002c0002t0002g0086 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2208+1999G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887010 | |||||||
| chr22:41887071 | T | C | 112 | a0001c0001t0001g0263 a0001c0001t0001g0286 a0001c0001t0004g0242 others(109): Show |
116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.2208+2060T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887071 | |||||||
| chr22:41887142 | G | A | 3 | a0001c0001t0003g0305 a0001c0001t0003g0306 a0001c0001t0003g0307 |
3 | HG01433.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2208+2131G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887142 | |||||||
| chr22:41887397 | C | T | 10 | a0004c0004t0001g0045 a0004c0004t0001g0053 a0004c0004t0001g0224 others(7): Show |
10 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2208+2386C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887397 | |||||||
| chr22:41887405 | C | T | 2 | a0003c0003t0004g0124 a0003c0003t0004g0125 |
2 | NA18939.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.2208+2394C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887405 | |||||||
| chr22:41887533 | G | A | 1 | a0009c0019t0001g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2208+2522G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887533 | |||||||
| chr22:41887546 | T | G | 52 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(49): Show |
55 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.2208+2535T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887546 | |||||||
| chr22:41887547 | A | T | 52 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(49): Show |
55 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.2208+2536A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887547 | |||||||
| chr22:41887705 | G | A | 37 | a0001c0001t0001g0263 a0001c0001t0001g0286 a0002c0002t0001g0032 others(34): Show |
38 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.2208+2694G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887705 | |||||||
| chr22:41887769 | C | T | 2 | a0002c0009t0002g0205 a0002c0009t0002g0223 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2208+2758C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887769 | |||||||
| chr22:41887838 | A | AT | 8 | a0002c0002t0006g0017 a0002c0002t0006g0018 a0002c0002t0006g0019 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2208+2834dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41887838 | ||||||
| chr22:41887838 | AT | A | 6 | a0002c0005t0005g0015 a0002c0005t0005g0243 a0002c0005t0005g0244 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2208+2834delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41887838 | ||||||
| chr22:41888256 | C | T | 61 | a0001c0001t0002g0256 a0001c0001t0003g0305 a0001c0001t0003g0306 others(58): Show |
62 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.2208+3245C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41888256 | |||||||
| chr22:41888469 | T | TCTG | 110 | a0001c0001t0001g0263 a0001c0001t0001g0286 a0002c0002t0001g0003 others(107): Show |
114 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.2208+3460_2208+346 others(7): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41888469 | ||||||
| chr22:41888862 | CT | C | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0198 |
3 | NA18947.hp2 NA18977.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.2208+3852delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41888862 | |||||||
| chr22:41888969 | T | G | 1 | a0004c0004t0005g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2208+3958T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41888969 | |||||||
| chr22:41889059 | A | T | 110 | a0001c0001t0001g0263 a0001c0001t0001g0286 a0002c0002t0001g0003 others(107): Show |
114 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.2208+4048A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889059 | |||||||
| chr22:41889073 | A | G | 1 | a0002c0002t0001g0121 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2209-4044A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889073 | |||||||
| chr22:41889097 | A | G | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2209-4020A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889097 | |||||||
| chr22:41889216 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2209-3901C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889216 | |||||||
| chr22:41889262 | G | A | 10 | a0002c0002t0003g0055 a0002c0002t0003g0056 a0002c0002t0006g0017 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2209-3855G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889262 | |||||||
| chr22:41889338 | G | T | 8 | a0002c0002t0006g0017 a0002c0002t0006g0018 a0002c0002t0006g0019 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2209-3779G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889338 | |||||||
| chr22:41889376 | C | T | 2 | a0001c0001t0011g0175 a0001c0001t0019g0176 |
2 | HG02155.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2209-3741C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889376 | |||||||
| chr22:41889486 | G | A | 1 | a0001c0001t0004g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2209-3631G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889486 | |||||||
| chr22:41889684 | T | G | 9 | a0002c0005t0005g0015 a0002c0005t0005g0016 a0002c0005t0005g0243 others(6): Show |
9 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2209-3433T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889684 | |||||||
| chr22:41889701 | TA | T | 236 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(233): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2209-3401delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41889701 | ||||||
| chr22:41889715 | AAG | A | 73 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(70): Show |
76 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.2209-3399_2209-339 others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41889715 | ||||||
| chr22:41889728 | C | T | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2209-3389C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889728 | |||||||
| chr22:41889810 | G | C | 8 | a0002c0002t0006g0017 a0002c0002t0006g0018 a0002c0002t0006g0019 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2209-3307G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889810 | |||||||
| chr22:41889830 | G | A | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2209-3287G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889830 | |||||||
| chr22:41889864 | C | G | 112 | a0001c0001t0001g0263 a0001c0001t0001g0286 a0002c0002t0001g0003 others(109): Show |
116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.2209-3253C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889864 | |||||||
| chr22:41889940 | G | A | 1 | a0004c0004t0005g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2209-3177G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889940 | |||||||
| chr22:41890003 | AAG | A | 10 | a0002c0005t0005g0015 a0002c0005t0005g0016 a0002c0005t0005g0243 others(7): Show |
10 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2209-3106_2209-310 others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41890003 | ||||||
| chr22:41890026 | T | G | 1 | a0001c0001t0001g0287 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2209-3091T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890026 | |||||||
| chr22:41890092 | T | A | 1 | a0008c0014t0005g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2209-3025T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890092 | |||||||
| chr22:41890176 | T | C | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2209-2941T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890176 | |||||||
| chr22:41890195 | A | C | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2209-2922A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890195 | |||||||
| chr22:41890251 | G | A | 37 | a0001c0001t0001g0263 a0001c0001t0001g0286 a0002c0002t0001g0032 others(34): Show |
38 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.2209-2866G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890251 | |||||||
| chr22:41890287 | C | T | 7 | a0002c0002t0002g0050 a0002c0002t0002g0080 a0002c0002t0002g0081 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2209-2830C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890287 | |||||||
| chr22:41890445 | G | A | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2209-2672G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890445 | |||||||
| chr22:41890672 | A | AT | 75 | a0001c0001t0001g0217 a0001c0001t0002g0324 a0001c0001t0003g0013 others(72): Show |
78 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.2209-2432dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41890672 | ||||||
| chr22:41890672 | A | ATT | 14 | a0001c0001t0001g0220 a0002c0002t0001g0137 a0002c0002t0003g0110 others(11): Show |
14 | HG01099.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.2209-2433_2209-243 others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41890672 | ||||||
| chr22:41890773 | T | C | 1 | a0003c0017t0004g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2209-2344T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890773 | |||||||
| chr22:41890882 | T | C | 1 | a0002c0002t0003g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2209-2235T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890882 | |||||||
| chr22:41891144 | C | T | 3 | a0004c0004t0009g0047 a0004c0004t0009g0048 a0004c0004t0009g0049 |
3 | HG02559.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2209-1973C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891144 | |||||||
| chr22:41891186 | C | T | 8 | a0001c0001t0001g0217 a0001c0001t0001g0220 a0001c0001t0003g0013 others(5): Show |
8 | HG01099.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2209-1931C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891186 | |||||||
| chr22:41891199 | C | G | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0214 |
3 | HG00733.hp1 HG01258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2209-1918C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891199 | |||||||
| chr22:41891301 | G | A | 1 | a0002c0002t0002g0084 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2209-1816G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891301 | |||||||
| chr22:41891364 | G | A | 2 | a0003c0003t0004g0124 a0003c0003t0004g0125 |
2 | NA18939.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.2209-1753G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891364 | |||||||
| chr22:41891450 | A | G | 244 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0069 others(241): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.2209-1667A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891450 | |||||||
| chr22:41891765 | T | A | 1 | a0002c0005t0015g0248 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2209-1352T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891765 | |||||||
| chr22:41891789 | T | C | 1 | a0002c0002t0001g0145 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2209-1328T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891789 | |||||||
| chr22:41891838 | T | C | 2 | a0002c0005t0005g0016 a0002c0005t0005g0246 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2209-1279T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891838 | |||||||
| chr22:41891851 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0001t0001g0179 others(2): Show |
6 | NA18747.hp1 NA18948.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.2209-1266A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891851 | |||||||
| chr22:41891902 | C | T | 4 | a0002c0002t0008g0317 a0002c0002t0008g0318 a0002c0002t0008g0319 others(1): Show |
4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2209-1215C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891902 | |||||||
| chr22:41891962 | C | T | 24 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0003c0003t0004g0096 others(21): Show |
24 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.2209-1155C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891962 | |||||||
| chr22:41892051 | C | G | 2 | a0001c0001t0012g0215 a0002c0002t0012g0057 |
2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2209-1066C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892051 | |||||||
| chr22:41892068 | A | G | 2 | a0003c0003t0004g0127 a0003c0003t0004g0136 |
2 | HG00099.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2209-1049A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892068 | |||||||
| chr22:41892126 | G | C | 4 | a0002c0002t0008g0317 a0002c0002t0008g0318 a0002c0002t0008g0319 others(1): Show |
4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2209-991G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892126 | |||||||
| chr22:41892137 | G | C | 1 | a0003c0017t0004g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2209-980G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892137 | |||||||
| chr22:41892256 | C | T | 5 | a0002c0002t0003g0001 a0002c0002t0003g0011 a0002c0002t0003g0058 others(2): Show |
6 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2209-861C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892256 | |||||||
| chr22:41892365 | A | C | 1 | a0001c0001t0001g0284 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2209-752A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892365 | |||||||
| chr22:41892477 | G | A | 1 | a0001c0001t0003g0219 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2209-640G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892477 | |||||||
| chr22:41892541 | G | A | 40 | a0001c0001t0004g0242 a0001c0001t0006g0021 a0001c0001t0013g0216 others(37): Show |
40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.2209-576G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892541 | |||||||
| chr22:41892562 | G | A | 5 | a0001c0001t0001g0251 a0001c0001t0001g0278 a0001c0001t0001g0301 others(2): Show |
5 | NA18946.hp1 NA18962.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.2209-555G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892562 | |||||||
| chr22:41892647 | C | CA | 149 | a0001c0001t0001g0168 a0001c0001t0001g0177 a0001c0001t0001g0178 others(146): Show |
151 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.2209-449dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41892647 | ||||||
| chr22:41892647 | C | CAA | 15 | a0001c0001t0001g0181 a0001c0001t0001g0217 a0002c0002t0001g0034 others(12): Show |
15 | HG01192.hp1 HG01261.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.2209-450_2209-449d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41892647 | ||||||
| chr22:41892647 | C | CAAA | 6 | a0001c0001t0012g0215 a0002c0002t0012g0057 a0002c0005t0015g0248 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2209-451_2209-449d others(5): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41892647 | ||||||
| chr22:41892647 | CA | C | 16 | a0001c0001t0001g0166 a0001c0001t0001g0171 a0001c0001t0001g0255 others(13): Show |
16 | HG01261.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.2209-449delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41892647 | ||||||
| chr22:41892745 | C | A | 12 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(9): Show |
12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2209-372C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892745 | |||||||
| chr22:41892990 | T | G | 56 | a0001c0001t0004g0242 a0001c0001t0006g0021 a0001c0001t0007g0113 others(53): Show |
56 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2209-127T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892990 | |||||||
| chr22:41893092 | A | G | 1 | a0001c0001t0002g0256 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2209-25A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41893092 | |||||||
| chr22:41893295 | C | G | 2 | a0002c0005t0005g0016 a0002c0005t0005g0246 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2377+10C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893295 | |||||||
| chr22:41893313 | T | C | 12 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(9): Show |
12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2377+28T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893313 | |||||||
| chr22:41893366 | C | T | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2377+81C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893366 | |||||||
| chr22:41893401 | C | CGTTT | 27 | a0001c0001t0001g0187 a0001c0001t0011g0210 a0001c0011t0001g0288 others(24): Show |
27 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.2377+142_2377+145d others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr22 | 41893401 | ||||||
| chr22:41893418 | G | T | 1 | a0001c0007t0003g0010 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2377+133G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893418 | |||||||
| chr22:41893462 | T | C | 56 | a0001c0001t0004g0242 a0001c0001t0006g0021 a0001c0001t0007g0113 others(53): Show |
56 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2377+177T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893462 | |||||||
| chr22:41893496 | G | A | 53 | a0001c0001t0002g0256 a0001c0001t0002g0324 a0001c0001t0014g0316 others(50): Show |
54 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.2377+211G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893496 | |||||||
| chr22:41893561 | C | T | 14 | a0001c0001t0006g0021 a0001c0001t0013g0216 a0002c0002t0005g0009 others(11): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2377+276C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893561 | |||||||
| chr22:41893793 | C | T | 24 | a0002c0018t0004g0156 a0003c0003t0004g0096 a0003c0003t0004g0106 others(21): Show |
24 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2377+508C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893793 | |||||||
| chr22:41893800 | A | G | 14 | a0001c0001t0006g0021 a0001c0001t0013g0216 a0002c0002t0005g0009 others(11): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2377+515A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893800 | |||||||
| chr22:41893969 | T | C | 1 | a0003c0003t0004g0117 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2377+684T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893969 | |||||||
| chr22:41894030 | C | T | 2 | a0001c0001t0012g0215 a0002c0002t0012g0057 |
2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2377+745C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41894030 | |||||||
| chr22:41894173 | T | C | 56 | a0001c0001t0004g0242 a0001c0001t0006g0021 a0001c0001t0007g0113 others(53): Show |
56 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2378-647T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41894173 | |||||||
| chr22:41894222 | C | T | 1 | a0004c0004t0010g0054 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2378-598C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41894222 | |||||||
| chr22:41894317 | G | A | 1 | a0002c0005t0005g0243 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2378-503G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41894317 | |||||||
| chr22:41894486 | C | T | 3 | a0002c0002t0003g0027 a0002c0002t0003g0029 a0002c0002t0003g0076 |
3 | HG00738.hp1 HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.2378-334C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41894486 | |||||||
| chr22:41894502 | T | C | 1 | a0003c0003t0004g0127 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2378-318T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41894502 | |||||||
| chr22:41894674 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2378-146T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41894674 | |||||||
| chr22:41895014 | C | T | 1 | a0002c0002t0001g0040 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2495+77C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895014 | |||||||
| chr22:41895118 | C | G | 12 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(9): Show |
12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2495+181C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895118 | |||||||
| chr22:41895140 | G | GT | 42 | a0001c0001t0001g0174 a0001c0001t0001g0182 a0001c0001t0001g0187 others(39): Show |
42 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.2495+219dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 41895140 | ||||||
| chr22:41895170 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2495+233C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895170 | |||||||
| chr22:41895240 | C | T | 12 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(9): Show |
12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2495+303C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895240 | |||||||
| chr22:41895330 | G | A | 1 | a0002c0002t0005g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2495+393G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895330 | |||||||
| chr22:41895403 | T | C | 1 | a0002c0013t0001g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2495+466T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895403 | |||||||
| chr22:41895431 | C | CT | 29 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0001c0001t0001g0184 others(26): Show |
29 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.2495+515dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 41895431 | ||||||
| chr22:41895431 | C | CTT | 9 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(6): Show |
9 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2495+514_2495+515d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 41895431 | ||||||
| chr22:41895453 | G | C | 5 | a0001c0007t0003g0010 a0001c0007t0003g0087 a0001c0007t0003g0088 others(2): Show |
5 | HG01934.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495+516G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895453 | |||||||
| chr22:41895466 | G | A | 5 | a0001c0001t0013g0216 a0002c0002t0005g0009 a0002c0002t0005g0051 others(2): Show |
5 | HG01884.hp1 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2495+529G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895466 | |||||||
| chr22:41895528 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2495+591C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895528 | |||||||
| chr22:41895588 | A | G | 1 | a0002c0002t0001g0129 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2495+651A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895588 | |||||||
| chr22:41895675 | A | G | 25 | a0001c0001t0004g0242 a0002c0018t0004g0156 a0003c0003t0004g0096 others(22): Show |
25 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.2495+738A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895675 | |||||||
| chr22:41895687 | C | T | 1 | a0004c0004t0005g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2495+750C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895687 | |||||||
| chr22:41895728 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2495+791G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895728 | |||||||
| chr22:41895852 | G | A | 24 | a0001c0001t0004g0242 a0002c0018t0004g0156 a0003c0003t0004g0096 others(21): Show |
24 | HG00099.hp1 HG00280.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.2495+915G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895852 | |||||||
| chr22:41895852 | G | C | 1 | a0003c0003t0004g0138 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2495+915G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895852 | |||||||
| chr22:41895875 | C | CA | 14 | a0001c0001t0006g0021 a0001c0001t0013g0216 a0002c0002t0005g0009 others(11): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2495+939dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 41895875 | ||||||
| chr22:41896073 | G | A | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2496-979G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896073 | |||||||
| chr22:41896106 | A | G | 1 | a0004c0004t0009g0049 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2496-946A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896106 | |||||||
| chr22:41896109 | C | G | 14 | a0001c0001t0006g0021 a0001c0001t0013g0216 a0002c0002t0005g0009 others(11): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2496-943C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896109 | |||||||
| chr22:41896274 | A | C | 30 | a0001c0001t0006g0021 a0001c0001t0007g0113 a0001c0001t0007g0240 others(27): Show |
30 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.2496-778A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896274 | |||||||
| chr22:41896363 | T | G | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2496-689T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896363 | |||||||
| chr22:41896487 | G | A | 1 | a0001c0001t0004g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2496-565G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896487 | |||||||
| chr22:41896655 | G | A | 1 | a0008c0014t0005g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2496-397G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896655 | |||||||
| chr22:41896739 | G | A | 4 | a0002c0002t0008g0317 a0002c0002t0008g0318 a0002c0002t0008g0319 others(1): Show |
4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2496-313G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896739 | |||||||
| chr22:41896881 | C | T | 24 | a0003c0003t0004g0096 a0003c0003t0004g0106 a0003c0003t0004g0117 others(21): Show |
24 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2496-171C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896881 | |||||||
| chr22:41896892 | C | T | 3 | a0003c0003t0004g0117 a0003c0010t0001g0146 a0005c0006t0004g0238 |
3 | HG00280.hp1 NA18952.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.2496-160C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896892 | |||||||
| chr22:41896918 | C | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0201 |
2 | HG02027.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.2496-134C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896918 | |||||||
| chr22:41896919 | G | A | 24 | a0003c0003t0004g0096 a0003c0003t0004g0106 a0003c0003t0004g0117 others(21): Show |
24 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2496-133G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896919 | |||||||
| chr22:41897011 | A | G | 1 | a0002c0002t0005g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2496-41A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41897011 | |||||||
| chr22:41897274 | A | G | 12 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(9): Show |
12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2605+113A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41897274 | |||||||
| chr22:41897431 | G | T | 1 | a0001c0001t0003g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2605+270G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41897431 | |||||||
| chr22:41898113 | T | A | 5 | a0002c0002t0003g0001 a0002c0002t0003g0011 a0002c0002t0003g0058 others(2): Show |
6 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2606-536T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41898113 | |||||||
| chr22:41898119 | A | AT | 14 | a0001c0001t0006g0021 a0001c0001t0013g0216 a0002c0002t0005g0009 others(11): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2606-522dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr22 | 41898119 | ||||||
| chr22:41898133 | G | A | 3 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 |
3 | HG03041.hp2 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2606-516G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41898133 | |||||||
| chr22:41898172 | A | G | 57 | a0001c0001t0001g0277 a0001c0001t0004g0242 a0001c0001t0006g0021 others(54): Show |
57 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.2606-477A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41898172 | |||||||
| chr22:41898249 | G | T | 1 | a0001c0001t0001g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2606-400G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41898249 | |||||||
| chr22:41898334 | T | C | 14 | a0001c0001t0006g0021 a0001c0001t0013g0216 a0002c0002t0005g0009 others(11): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2606-315T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41898334 | |||||||
| chr22:41898609 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2606-40C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41898609 | |||||||
| chr22:41898867 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2738+86G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41898867 | |||||||
| chr22:41899174 | A | G | 5 | a0002c0002t0002g0118 a0002c0002t0002g0148 a0002c0002t0002g0149 others(2): Show |
5 | HG00642.hp2 HG02735.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.2738+393A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899174 | |||||||
| chr22:41899246 | C | G | 85 | a0001c0001t0001g0099 a0001c0001t0001g0128 a0001c0001t0001g0162 others(82): Show |
85 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.2738+465C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899246 | |||||||
| chr22:41899507 | C | T | 4 | a0002c0002t0008g0317 a0002c0002t0008g0318 a0002c0002t0008g0319 others(1): Show |
4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2738+726C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899507 | |||||||
| chr22:41899604 | C | T | 1 | a0001c0001t0004g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2739-726C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899604 | |||||||
| chr22:41899649 | G | A | 23 | a0002c0018t0004g0156 a0003c0003t0004g0096 a0003c0003t0004g0106 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.2739-681G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899649 | |||||||
| chr22:41899753 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0296 |
2 | NA18939.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.2739-577C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899753 | |||||||
| chr22:41899965 | G | T | 2 | a0001c0001t0012g0215 a0002c0002t0012g0057 |
2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2739-365G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899965 | |||||||
| chr22:41899966 | G | C | 22 | a0002c0018t0004g0156 a0003c0003t0004g0096 a0003c0003t0004g0106 others(19): Show |
22 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.2739-364G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899966 | |||||||
| chr22:41899988 | G | A | 1 | a0001c0012t0001g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2739-342G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899988 | |||||||
| chr22:41900138 | G | A | 12 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(9): Show |
12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2739-192G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41900138 | |||||||
| chr22:41900175 | G | C | 13 | a0001c0001t0004g0242 a0001c0001t0007g0113 a0001c0001t0007g0240 others(10): Show |
13 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2739-155G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41900175 | |||||||
| chr22:41900218 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2739-112G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41900218 | |||||||
| chr22:41900580 | C | G | 10 | a0002c0002t0002g0050 a0002c0002t0002g0079 a0002c0002t0002g0080 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2907+82C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41900580 | |||||||
| chr22:41900604 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2907+106C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41900604 | |||||||
| chr22:41900699 | T | C | 56 | a0001c0001t0004g0242 a0001c0001t0006g0021 a0001c0001t0007g0113 others(53): Show |
56 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2907+201T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41900699 | |||||||
| chr22:41900929 | C | T | 13 | a0001c0001t0004g0242 a0001c0001t0007g0113 a0001c0001t0007g0240 others(10): Show |
13 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2907+431C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41900929 | |||||||
| chr22:41901187 | T | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0001c0001t0001g0202 others(3): Show |
6 | HG00673.hp2 NA18953.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2907+689T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901187 | |||||||
| chr22:41901210 | G | A | 14 | a0001c0001t0006g0021 a0001c0001t0013g0216 a0002c0002t0005g0009 others(11): Show |
14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2907+712G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901210 | |||||||
| chr22:41901298 | G | T | 4 | a0002c0002t0008g0317 a0002c0002t0008g0318 a0002c0002t0008g0319 others(1): Show |
4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2907+800G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901298 | |||||||
| chr22:41901459 | G | A | 12 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(9): Show |
12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2907+961G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901459 | |||||||
| chr22:41901748 | G | A | 10 | a0002c0002t0002g0050 a0002c0002t0002g0079 a0002c0002t0002g0080 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2908-1222G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901748 | |||||||
| chr22:41901768 | G | A | 1 | a0002c0002t0005g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2908-1202G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901768 | |||||||
| chr22:41901918 | G | A | 22 | a0002c0018t0004g0156 a0003c0003t0004g0096 a0003c0003t0004g0106 others(19): Show |
22 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.2908-1052G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901918 | |||||||
| chr22:41901937 | T | C | 1 | a0001c0024t0001g0257 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2908-1033T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901937 | |||||||
| chr22:41901964 | T | C | 55 | a0001c0001t0004g0242 a0001c0001t0006g0021 a0001c0001t0007g0113 others(52): Show |
55 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.2908-1006T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901964 | |||||||
| chr22:41902095 | A | T | 2 | a0001c0001t0003g0013 a0002c0002t0003g0110 |
2 | HG01496.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2908-875A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902095 | |||||||
| chr22:41902161 | C | T | 23 | a0002c0018t0004g0156 a0003c0003t0004g0096 a0003c0003t0004g0106 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.2908-809C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902161 | |||||||
| chr22:41902227 | C | T | 1 | a0002c0002t0002g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2908-743C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902227 | |||||||
| chr22:41902342 | G | A | 1 | a0002c0002t0006g0018 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2908-628G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902342 | |||||||
| chr22:41902392 | G | T | 1 | a0001c0001t0001g0008 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2908-578G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902392 | |||||||
| chr22:41902397 | A | T | 1 | a0002c0005t0015g0248 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2908-573A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902397 | |||||||
| chr22:41902400 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2908-570C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902400 | |||||||
| chr22:41902403 | A | T | 1 | a0003c0010t0021g0025 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2908-567A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902403 | |||||||
| chr22:41902410 | G | T | 1 | a0001c0001t0001g0285 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2908-560G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902410 | |||||||
| chr22:41902534 | A | C | 4 | a0002c0005t0005g0015 a0002c0005t0005g0245 a0002c0005t0005g0247 others(1): Show |
4 | HG02486.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2908-436A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902534 | |||||||
| chr22:41902582 | T | C | 1 | a0008c0014t0005g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2908-388T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902582 | |||||||
| chr22:41902597 | C | T | 23 | a0002c0018t0004g0156 a0003c0003t0004g0096 a0003c0003t0004g0106 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.2908-373C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902597 | |||||||
| chr22:41902678 | G | A | 3 | a0002c0002t0003g0326 a0002c0002t0003g0327 a0002c0002t0003g0328 |
3 | HG03225.hp1 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2908-292G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902678 | |||||||
| chr22:41902771 | C | T | 5 | a0001c0001t0001g0252 a0001c0001t0001g0283 a0001c0001t0001g0285 others(2): Show |
5 | NA18973.hp1 NA18988.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.2908-199C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902771 | |||||||
| chr22:41902820 | G | A | 3 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 |
3 | HG01934.hp1 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.2908-150G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902820 | |||||||
| chr22:41902902 | G | A | 1 | a0003c0003t0004g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2908-68G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902902 | |||||||
| chr22:41903173 | G | C | 1 | a0003c0003t0004g0132 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3093+18G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41903173 | |||||||
| chr22:41903417 | CAG | C | 7 | a0002c0002t0008g0317 a0002c0002t0008g0318 a0002c0002t0008g0319 others(4): Show |
7 | HG00099.hp1 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.3093+263_3093+264d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41903417 | |||||||
| chr22:41903522 | T | C | 5 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0119 others(2): Show |
7 | NA18965.hp2 NA18980.hp1 NA18990.hp2 others(4): Show |
intron_variant | MODIFIER | c.3093+367T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41903522 | |||||||
| chr22:41903531 | A | G | 53 | a0001c0001t0002g0256 a0001c0001t0002g0324 a0001c0001t0014g0316 others(50): Show |
54 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.3093+376A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41903531 | |||||||
| chr22:41903806 | G | A | 12 | a0001c0001t0007g0113 a0001c0001t0007g0240 a0001c0001t0007g0241 others(9): Show |
12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3093+651G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41903806 | |||||||
| chr22:41903813 | T | C | 29 | a0001c0001t0004g0242 a0002c0002t0008g0317 a0002c0002t0008g0318 others(26): Show |
29 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.3093+658T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41903813 | |||||||
| chr22:41904058 | A | G | 26 | a0001c0001t0006g0021 a0001c0001t0007g0113 a0001c0001t0007g0240 others(23): Show |
26 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.3094-805A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41904058 | |||||||
| chr22:41904169 | C | T | 26 | a0001c0001t0006g0021 a0001c0001t0007g0113 a0001c0001t0007g0240 others(23): Show |
26 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.3094-694C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41904169 | |||||||
| chr22:41904200 | A | C | 2 | a0001c0001t0012g0215 a0002c0002t0012g0057 |
2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3094-663A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41904200 | |||||||
| chr22:41904244 | C | G | 28 | a0001c0001t0004g0242 a0002c0002t0008g0317 a0002c0002t0008g0318 others(25): Show |
28 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.3094-619C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41904244 | |||||||
| chr22:41904407 | C | T | 5 | a0001c0001t0004g0242 a0002c0002t0008g0317 a0002c0002t0008g0318 others(2): Show |
5 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3094-456C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41904407 | |||||||
| chr22:41904424 | TCTTC | T | 23 | a0002c0018t0004g0156 a0003c0003t0004g0096 a0003c0003t0004g0106 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.3094-435_3094-432d others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr22 | 41904424 | ||||||
| chr22:41904470 | A | C | 1 | a0004c0004t0005g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3094-393A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41904470 | |||||||
| chr22:41905010 | A | G | 38 | a0001c0001t0004g0242 a0001c0001t0007g0113 a0001c0001t0007g0240 others(35): Show |
38 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.3205+36A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 18/18 | chr22 | 41905010 | |||||||
| chr22:41905129 | T | C | 54 | a0001c0001t0002g0256 a0001c0001t0002g0324 a0001c0001t0014g0316 others(51): Show |
55 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.3205+155T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 18/18 | chr22 | 41905129 | |||||||
| chr22:41905153 | A | G | 1 | a0002c0002t0007g0329 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3205+179A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 18/18 | chr22 | 41905153 | |||||||
| chr22:41905328 | C | T | 7 | a0001c0001t0001g0168 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
7 | NA18947.hp2 NA18961.hp2 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.3206-112C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 18/18 | chr22 | 41905328 | |||||||
| chr22:41905430 | C | T | 13 | a0001c0007t0003g0010 a0001c0007t0003g0087 a0001c0007t0003g0088 others(10): Show |
14 | HG00738.hp1 HG00741.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.3206-10C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 18/18 | chr22 | 41905430 |