Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6295 |
| ensemblid | ENSG00000130561.17 |
| hgncid | 10521 |
| symbol | SAG |
| name | S-antigen visual arrestin |
| refseq_nuc | NM_000541.5 |
| refseq_prot | NP_000532.2 |
| ensembl_nuc | ENST00000409110.6 |
| ensembl_prot | ENSP00000386444.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 233307816 |
| end | 233347055 |
| strand | + |
| ver | v1.2 |
| region | chr2:233307816-233347055 |
| region5000 | chr2:233302816-233352055 |
| regionname0 | SAG_chr2_233307816_233347055 |
| regionname5000 | SAG_chr2_233302816_233352055 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 405 | 202 | 52 | 44 | 86 | 7 | 11 | 68 | SAG_chr2_233302816_233352055 | SAG | MAASG others(400): Show |
chr2 | 233302816 | 233352055 |
| a0002 | 0/0 | 405 | 131 | 24 | 24 | 64 | 5 | 14 | 48 | SAG_chr2_233302816_233352055 | SAG | MAASG others(400): Show |
chr2 | 233302816 | 233352055 |
| a0003 | 0/0 | 405 | 23 | 7 | 0 | 12 | 0 | 4 | 12 | SAG_chr2_233302816_233352055 | SAG | MAASG others(400): Show |
chr2 | 233302816 | 233352055 |
| a0004 | 0/0 | 405 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | MAASG others(400): Show |
chr2 | 233302816 | 233352055 |
| a0005 | 0/0 | 405 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | MAASG others(400): Show |
chr2 | 233302816 | 233352055 |
| a0006 | 0/0 | 405 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | MAASG others(400): Show |
chr2 | 233302816 | 233352055 |
| a0007 | 0/0 | 405 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | MAASG others(400): Show |
chr2 | 233302816 | 233352055 |
| a0008 | 0/0 | 405 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | MAASG others(400): Show |
chr2 | 233302816 | 233352055 |
| a0009 | 0/0 | 405 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | MAASG others(400): Show |
chr2 | 233302816 | 233352055 |
| a0010 | 0/0 | 405 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | MAASG others(400): Show |
chr2 | 233302816 | 233352055 |
| a0011 | 0/0 | 405 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | MAASG others(400): Show |
chr2 | 233302816 | 233352055 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1215 | 170 | 33 | 40 | 81 | 4 | 10 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0001c0003 | 0/0 | 1215 | 25 | 13 | 3 | 5 | 3 | 1 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0001c0006 | 0/0 | 1215 | 6 | 6 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0001c0019 | 0/0 | 1215 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0002c0002 | 0/0 | 1215 | 97 | 5 | 18 | 58 | 5 | 11 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0002c0005 | 0/0 | 1215 | 19 | 9 | 4 | 4 | 0 | 2 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0002c0007 | 0/0 | 1215 | 5 | 3 | 0 | 1 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0002c0009 | 0/0 | 1215 | 4 | 4 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0002c0010 | 0/0 | 1215 | 4 | 3 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0002c0011 | 0/0 | 1215 | 2 | 0 | 2 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0003c0004 | 0/0 | 1215 | 22 | 6 | 0 | 12 | 0 | 4 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0003c0016 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0004c0008 | 0/0 | 1215 | 5 | 5 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0005c0012 | 0/0 | 1215 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0006c0014 | 0/0 | 1215 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0007c0017 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0008c0020 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0009c0018 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0010c0015 | 0/0 | 1215 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 | ||
| a0011c0013 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | ATGGC others(1210): Show |
chr2 | 233302816 | 233352055 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1596 | 154 | 31 | 32 | 77 | 4 | 9 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0001c0001t0002 | 0/1 | 1596 | 10 | 0 | 6 | 3 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0001c0001t0003 | 0/0 | 1596 | 3 | 0 | 2 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0001c0001t0005 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0001c0001t0006 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0001c0001t0007 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0001c0003t0001 | 0/0 | 1596 | 21 | 13 | 3 | 1 | 3 | 1 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0001c0003t0003 | 0/0 | 1596 | 4 | 0 | 0 | 4 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0001c0006t0001 | 0/0 | 1596 | 6 | 6 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0001c0019t0001 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0002c0002t0001 | 0/0 | 1596 | 96 | 5 | 18 | 57 | 5 | 11 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0002c0002t0004 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0002c0005t0001 | 0/0 | 1596 | 19 | 9 | 4 | 4 | 0 | 2 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0002c0007t0001 | 0/0 | 1596 | 5 | 3 | 0 | 1 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0002c0009t0001 | 0/0 | 1596 | 4 | 4 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0002c0010t0001 | 0/0 | 1596 | 4 | 3 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0002c0011t0001 | 0/0 | 1596 | 2 | 0 | 2 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0003c0004t0001 | 0/0 | 1596 | 21 | 6 | 0 | 12 | 0 | 3 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0003c0004t0004 | 0/0 | 1596 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0003c0016t0001 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0004c0008t0001 | 0/0 | 1596 | 5 | 5 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0005c0012t0001 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0006c0014t0001 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0007c0017t0001 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0008c0020t0001 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0009c0018t0001 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0010c0015t0001 | 0/0 | 1596 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| a0011c0013t0001 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | GAGAC others(1591): Show |
chr2 | 233302816 | 233352055 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0276 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0002g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0006t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0006t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0006t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0006t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0006t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0006t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0001c0019t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0002 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0002t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0005t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0007t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0007t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0007t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0007t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0007t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0009t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0009t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0009t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0009t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0010t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0010t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0010t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0010t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0011t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0002c0011t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0004t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0003c0016t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0004c0008t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0004c0008t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0004c0008t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0004c0008t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0005c0012t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0006c0014t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0007c0017t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0008c0020t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0009c0018t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0010c0015t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| a0011c0013t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0091 | EUR | GBR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0163 | EUR | GBR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0172 | EUR | FIN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0093 | EUR | FIN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0291 | EUR | FIN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0330 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0165 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0339 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0182 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0187 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0290 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG00741 | hp2 | a0002 | c0011 | t0001 | g0155 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0124 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0183 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01106 | hp2 | a0001 | c0019 | t0001 | g0169 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0160 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01175 | hp2 | a0005 | c0012 | t0001 | g0007 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0166 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0150 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01261 | hp1 | a0002 | c0011 | t0001 | g0167 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0092 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0317 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0177 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0216 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01433 | hp2 | a0002 | c0005 | t0001 | g0244 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01496 | hp1 | a0006 | c0014 | t0001 | g0146 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0170 | EUR | IBS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0095 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01934 | hp2 | a0002 | c0005 | t0001 | g0194 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01981 | hp1 | a0002 | c0005 | t0001 | g0268 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0332 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02055 | hp1 | a0007 | c0017 | t0001 | g0299 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0338 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02129 | hp2 | a0001 | c0003 | t0001 | g0337 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02145 | hp1 | a0002 | c0009 | t0001 | g0311 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CDX | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | CDX | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0331 | EAS | CDX | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02257 | hp1 | a0002 | c0010 | t0001 | g0085 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0096 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02258 | hp1 | a0002 | c0009 | t0001 | g0280 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02258 | hp2 | a0008 | c0020 | t0001 | g0147 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02300 | hp2 | a0002 | c0005 | t0001 | g0199 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02572 | hp2 | a0003 | c0004 | t0001 | g0185 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0081 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02622 | hp2 | a0002 | c0007 | t0001 | g0083 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0186 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02717 | hp1 | a0004 | c0008 | t0001 | g0108 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0094 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0296 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0162 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0174 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0079 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02818 | hp1 | a0003 | c0004 | t0001 | g0006 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02818 | hp2 | a0004 | c0008 | t0001 | g0075 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02896 | hp1 | a0003 | c0004 | t0001 | g0318 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0099 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02897 | hp2 | a0003 | c0004 | t0001 | g0319 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02922 | hp1 | a0002 | c0005 | t0001 | g0005 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02922 | hp2 | a0001 | c0006 | t0001 | g0286 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02965 | hp1 | a0002 | c0005 | t0001 | g0283 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02965 | hp2 | a0002 | c0007 | t0001 | g0073 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02970 | hp1 | a0004 | c0008 | t0001 | g0003 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02970 | hp2 | a0002 | c0007 | t0001 | g0080 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02976 | hp1 | a0002 | c0009 | t0001 | g0078 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02976 | hp2 | a0002 | c0005 | t0001 | g0005 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0040 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0082 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03098 | hp2 | a0009 | c0018 | t0001 | g0191 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03130 | hp1 | a0001 | c0006 | t0001 | g0121 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03130 | hp2 | a0003 | c0004 | t0001 | g0006 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03139 | hp1 | a0004 | c0008 | t0001 | g0076 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03209 | hp1 | a0002 | c0010 | t0001 | g0102 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0100 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0097 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03239 | hp1 | a0003 | c0004 | t0001 | g0137 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0320 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03453 | hp1 | a0002 | c0005 | t0001 | g0312 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03453 | hp2 | a0001 | c0006 | t0001 | g0122 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03486 | hp2 | a0002 | c0005 | t0001 | g0313 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0171 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03490 | hp2 | a0003 | c0004 | t0004 | g0294 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03516 | hp2 | a0001 | c0006 | t0001 | g0292 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03540 | hp2 | a0003 | c0004 | t0001 | g0130 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03579 | hp1 | a0003 | c0016 | t0001 | g0133 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0101 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03669 | hp1 | a0010 | c0015 | t0001 | g0057 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03669 | hp2 | a0002 | c0005 | t0001 | g0298 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0125 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0321 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0153 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03704 | hp2 | a0003 | c0004 | t0001 | g0135 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0090 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | BEB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0335 | SAS | BEB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0127 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0158 | SAS | BEB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG04184 | hp2 | a0002 | c0005 | t0001 | g0039 | SAS | BEB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0173 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG04228 | hp2 | a0003 | c0004 | t0001 | g0136 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18522 | hp1 | a0002 | c0005 | t0001 | g0282 | AFR | YRI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18522 | hp2 | a0001 | c0006 | t0001 | g0279 | AFR | YRI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18906 | hp2 | a0001 | c0006 | t0001 | g0118 | AFR | YRI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18940 | hp2 | a0001 | c0003 | t0003 | g0088 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18944 | hp1 | a0003 | c0004 | t0001 | g0138 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18944 | hp2 | a0002 | c0005 | t0001 | g0009 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18948 | hp2 | a0002 | c0002 | t0004 | g0343 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0333 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18956 | hp2 | a0001 | c0003 | t0003 | g0258 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18959 | hp2 | a0003 | c0004 | t0001 | g0106 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18966 | hp1 | a0003 | c0004 | t0001 | g0139 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18967 | hp1 | a0003 | c0004 | t0001 | g0295 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18968 | hp1 | a0002 | c0010 | t0001 | g0289 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18968 | hp2 | a0003 | c0004 | t0001 | g0134 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0344 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18971 | hp1 | a0002 | c0005 | t0001 | g0009 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18977 | hp2 | a0003 | c0004 | t0001 | g0141 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0328 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18981 | hp2 | a0003 | c0004 | t0001 | g0132 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18984 | hp1 | a0002 | c0005 | t0001 | g0301 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18989 | hp1 | a0003 | c0004 | t0001 | g0143 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0326 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18997 | hp1 | a0001 | c0003 | t0003 | g0086 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0342 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19011 | hp2 | a0001 | c0003 | t0003 | g0087 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19030 | hp1 | a0002 | c0010 | t0001 | g0068 | AFR | LWK | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19043 | hp1 | a0011 | c0013 | t0001 | g0285 | AFR | LWK | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | LWK | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19056 | hp2 | a0003 | c0004 | t0001 | g0129 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19059 | hp1 | a0003 | c0004 | t0001 | g0131 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19059 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0341 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0340 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19081 | hp2 | a0003 | c0004 | t0001 | g0140 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19086 | hp1 | a0002 | c0007 | t0001 | g0072 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19088 | hp2 | a0002 | c0005 | t0001 | g0300 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19089 | hp2 | a0003 | c0004 | t0001 | g0142 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0098 | AFR | YRI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA19240 | hp2 | a0002 | c0005 | t0001 | g0281 | AFR | YRI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA20129 | hp1 | a0002 | c0005 | t0001 | g0284 | AFR | ASW | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ASW | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0184 | EUR | TSI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | GIH | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA20905 | hp2 | a0002 | c0007 | t0001 | g0089 | SAS | GIH | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03471 | hp1 | a0002 | c0009 | t0001 | g0288 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0069 | AFR | USA | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0188 | AFR | USA | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA20300 | hp2 | a0002 | c0005 | t0001 | g0287 | AFR | USA | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA21309 | hp1 | a0004 | c0008 | t0001 | g0003 | AFR | LWK | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | LWK | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0229 | REF | REF | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0276 | REF | REF | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:233309224 | C | T | 1 | a0008 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.35C>T | p.Pro12Leu | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/16 | 270/1596 | 35/1218 | 12/405 | chr2 | 233309224 | |||
| chr2:233320674 | A | G | 3 | a0003 a0007 a0009 |
25 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(22): Show |
missense_variant | MODERATE | c.226A>G | p.Ile76Val | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/16 | 461/1596 | 226/1218 | 76/405 | chr2 | 233320674 | |||
| chr2:233320698 | C | T | 1 | a0004 | 5 | HG02717.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.250C>T | p.Arg84Cys | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/16 | 485/1596 | 250/1218 | 84/405 | chr2 | 233320698 | |||
| chr2:233320749 | G | A | 1 | a0005 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.301G>A | p.Ala101Thr | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/16 | 536/1596 | 301/1218 | 101/405 | chr2 | 233320749 | |||
| chr2:233327173 | C | A | 1 | a0011 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.488C>A | p.Ala163Asp | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/16 | 723/1596 | 488/1218 | 163/405 | chr2 | 233327173 | |||
| chr2:233327196 | A | G | 1 | a0010 | 1 | HG03669.hp1 | missense_variant&splice_region_variant | MODERATE | c.511A>G | p.Lys171Glu | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/16 | 746/1596 | 511/1218 | 171/405 | chr2 | 233327196 | |||
| chr2:233342315 | C | T | 1 | a0009 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.1091C>T | p.Pro364Leu | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/16 | 1326/1596 | 1091/1218 | 364/405 | chr2 | 233342315 | |||
| chr2:233346826 | G | A | 1 | a0006 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.1132G>A | p.Val378Ile | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 16/16 | 1367/1596 | 1132/1218 | 378/405 | chr2 | 233346826 | |||
| chr2:233346901 | G | A | 6 | a0002 a0003 a0005 others(3): Show |
107 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(104): Show |
missense_variant | MODERATE | c.1207G>A | p.Val403Ile | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 16/16 | 1442/1596 | 1207/1218 | 403/405 | chr2 | 233346901 | |||
| chr2:233346902 | T | C | 4 | a0002 a0003 a0009 others(1): Show |
53 | HG00741.hp2 HG01261.hp1 HG01433.hp2 others(50): Show |
missense_variant | MODERATE | c.1208T>C | p.Val403Ala | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 16/16 | 1443/1596 | 1208/1218 | 403/405 | chr2 | 233346902 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:233320649 | C | T | 2 | a0001c0019 a0002c0011 |
3 | HG00741.hp2 HG01106.hp2 HG01261.hp1 |
synonymous_variant | LOW | c.201C>T | p.Cys67Cys | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/16 | 436/1596 | 201/1218 | 67/405 | chr2 | 233320649 | |||
| chr2:233320679 | C | T | 1 | a0004c0008 | 5 | HG02717.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
synonymous_variant | LOW | c.231C>T | p.Asp77Asp | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/16 | 466/1596 | 231/1218 | 77/405 | chr2 | 233320679 | |||
| chr2:233320769 | G | C | 2 | a0001c0006 a0002c0009 |
10 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(7): Show |
synonymous_variant | LOW | c.321G>C | p.Leu107Leu | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/16 | 556/1596 | 321/1218 | 107/405 | chr2 | 233320769 | |||
| chr2:233327174 | C | T | 3 | a0001c0003 a0002c0007 a0002c0010 |
34 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
synonymous_variant | LOW | c.489C>T | p.Ala163Ala | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/16 | 724/1596 | 489/1218 | 163/405 | chr2 | 233327174 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:233307828 | C | G | 1 | a0001c0001t0007 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-223C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/16 | 1362 | chr2 | 233307828 | ||||||
| chr2:233307949 | T | C | 1 | a0001c0001t0005 | 1 | NA19002.hp2 | 5_prime_UTR_variant | MODIFIER | c.-102T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/16 | 1241 | chr2 | 233307949 | ||||||
| chr2:233307982 | G | A | 1 | a0001c0001t0006 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/16 | 1208 | chr2 | 233307982 | ||||||
| chr2:233346919 | C | T | 2 | a0001c0001t0002 a0001c0001t0005 |
10 | HG00621.hp1 HG00735.hp2 HG01168.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 16/16 | 7 | chr2 | 233346919 | ||||||
| chr2:233347001 | C | T | 2 | a0001c0001t0003 a0001c0003t0003 |
7 | HG00639.hp1 HG01346.hp2 HG03688.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*89C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 16/16 | 89 | chr2 | 233347001 | ||||||
| chr2:233347002 | G | A | 2 | a0002c0002t0004 a0003c0004t0004 |
2 | HG03490.hp2 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*90G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 16/16 | 90 | chr2 | 233347002 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:233308081 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-29+59G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308081 | |||||||
| chr2:233308220 | G | C | 1 | a0001c0001t0001g0019 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-29+198G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308220 | |||||||
| chr2:233308271 | G | A | 34 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(31): Show |
34 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.-29+249G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308271 | |||||||
| chr2:233308276 | A | G | 1 | a0001c0001t0001g0347 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-29+254A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308276 | |||||||
| chr2:233308296 | C | CA | 10 | a0001c0001t0001g0054 a0002c0002t0001g0055 a0002c0002t0001g0056 others(7): Show |
10 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.-29+281dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 233308296 | ||||||
| chr2:233308394 | G | A | 8 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(5): Show |
8 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29+372G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308394 | |||||||
| chr2:233308399 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-29+377C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308399 | |||||||
| chr2:233308406 | G | A | 2 | a0002c0007t0001g0072 a0002c0007t0001g0073 |
2 | HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-29+384G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308406 | |||||||
| chr2:233308548 | T | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0077 others(4): Show |
8 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+526T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308548 | |||||||
| chr2:233308575 | T | C | 1 | a0002c0009t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-29+553T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308575 | |||||||
| chr2:233308603 | T | A | 44 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(41): Show |
46 | HG00140.hp1 HG00280.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.-28-559T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308603 | |||||||
| chr2:233308800 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-28-362G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308800 | |||||||
| chr2:233308811 | C | T | 1 | a0001c0001t0001g0345 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-28-351C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308811 | |||||||
| chr2:233308816 | A | G | 24 | a0001c0003t0001g0337 a0002c0002t0001g0016 a0002c0002t0001g0322 others(21): Show |
25 | HG00558.hp1 HG00673.hp1 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.-28-346A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308816 | |||||||
| chr2:233308817 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-28-345C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308817 | |||||||
| chr2:233309033 | C | G | 2 | a0002c0007t0001g0072 a0002c0007t0001g0073 |
2 | HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-28-129C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233309033 | |||||||
| chr2:233309036 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-28-126G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233309036 | |||||||
| chr2:233309092 | T | G | 1 | a0003c0004t0001g0106 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-28-70T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233309092 | |||||||
| chr2:233309299 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.75+35T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233309299 | |||||||
| chr2:233309451 | C | T | 1 | a0002c0002t0001g0344 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.75+187C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233309451 | |||||||
| chr2:233309466 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.75+202G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233309466 | |||||||
| chr2:233309535 | C | T | 3 | a0002c0002t0001g0002 a0002c0002t0001g0320 a0002c0002t0001g0321 |
6 | HG01069.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+271C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233309535 | |||||||
| chr2:233309595 | A | C | 1 | a0001c0001t0001g0019 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.75+331A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233309595 | |||||||
| chr2:233309895 | C | T | 1 | a0002c0010t0001g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.75+631C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233309895 | |||||||
| chr2:233309978 | A | G | 2 | a0003c0004t0001g0318 a0003c0004t0001g0319 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.75+714A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233309978 | |||||||
| chr2:233310087 | A | G | 4 | a0001c0001t0001g0103 a0001c0003t0001g0317 a0002c0007t0001g0072 others(1): Show |
4 | HG01358.hp2 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+823A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310087 | |||||||
| chr2:233310185 | G | A | 1 | a0004c0008t0001g0108 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+921G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310185 | |||||||
| chr2:233310196 | G | A | 4 | a0001c0001t0001g0103 a0001c0003t0001g0317 a0002c0007t0001g0072 others(1): Show |
4 | HG01358.hp2 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+932G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310196 | |||||||
| chr2:233310241 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.75+977T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310241 | |||||||
| chr2:233310391 | T | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0347 others(3): Show |
7 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1127T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310391 | |||||||
| chr2:233310501 | T | C | 2 | a0002c0007t0001g0072 a0002c0007t0001g0073 |
2 | HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.75+1237T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310501 | |||||||
| chr2:233310506 | C | CT | 42 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(39): Show |
44 | HG01109.hp2 HG01358.hp2 HG02055.hp1 others(41): Show |
intron_variant | MODIFIER | c.75+1263dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233310506 | ||||||
| chr2:233310506 | C | CTT | 8 | a0001c0001t0001g0053 a0001c0001t0001g0071 a0001c0001t0001g0103 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+1262_75+1263dup others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233310506 | ||||||
| chr2:233310506 | CT | C | 18 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0074 others(15): Show |
19 | HG01168.hp1 HG01257.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.75+1263delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233310506 | ||||||
| chr2:233310556 | C | CTGGAG | 3 | a0002c0002t0001g0002 a0002c0002t0001g0320 a0002c0002t0001g0321 |
6 | HG01069.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+1295_75+1299dup others(5): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233310556 | ||||||
| chr2:233310684 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.75+1420T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310684 | |||||||
| chr2:233310863 | C | T | 1 | a0003c0004t0004g0294 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.75+1599C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310863 | |||||||
| chr2:233310928 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.75+1664C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310928 | |||||||
| chr2:233310953 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.75+1689G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310953 | |||||||
| chr2:233310994 | C | T | 2 | a0001c0006t0001g0118 a0001c0006t0001g0292 |
2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.75+1730C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310994 | |||||||
| chr2:233311306 | G | A | 5 | a0001c0003t0001g0004 a0001c0003t0001g0081 a0001c0003t0001g0082 others(2): Show |
6 | HG02615.hp1 HG02622.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+2042G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233311306 | |||||||
| chr2:233311386 | C | T | 2 | a0002c0007t0001g0072 a0002c0007t0001g0073 |
2 | HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.75+2122C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233311386 | |||||||
| chr2:233311511 | C | T | 43 | a0001c0001t0001g0103 a0001c0003t0001g0004 a0001c0003t0001g0079 others(40): Show |
44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.75+2247C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233311511 | |||||||
| chr2:233311589 | G | T | 8 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(5): Show |
8 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+2325G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233311589 | |||||||
| chr2:233311595 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0077 others(4): Show |
8 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+2331G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233311595 | |||||||
| chr2:233311782 | C | G | 2 | a0003c0004t0001g0318 a0003c0004t0001g0319 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.75+2518C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233311782 | |||||||
| chr2:233312083 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.75+2819G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312083 | |||||||
| chr2:233312105 | A | G | 1 | a0001c0006t0001g0279 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+2841A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312105 | |||||||
| chr2:233312215 | C | G | 2 | a0003c0004t0001g0318 a0003c0004t0001g0319 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.75+2951C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312215 | |||||||
| chr2:233312285 | A | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0104 others(8): Show |
13 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+3021A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312285 | |||||||
| chr2:233312546 | C | T | 61 | a0001c0001t0001g0019 a0001c0001t0001g0064 a0001c0001t0001g0065 others(58): Show |
63 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.75+3282C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312546 | |||||||
| chr2:233312655 | A | G | 10 | a0001c0001t0001g0054 a0002c0002t0001g0055 a0002c0002t0001g0056 others(7): Show |
10 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+3391A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312655 | |||||||
| chr2:233312657 | C | T | 2 | a0001c0003t0001g0290 a0001c0003t0001g0291 |
2 | HG00323.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.75+3393C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312657 | |||||||
| chr2:233312703 | C | T | 7 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0077 others(4): Show |
8 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-3372C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312703 | |||||||
| chr2:233313041 | T | C | 60 | a0001c0001t0001g0019 a0001c0001t0001g0064 a0001c0001t0001g0065 others(57): Show |
62 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.76-3034T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233313041 | |||||||
| chr2:233313099 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.76-2976C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233313099 | |||||||
| chr2:233313289 | G | T | 27 | a0001c0003t0001g0004 a0001c0003t0001g0079 a0001c0003t0001g0081 others(24): Show |
28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.76-2786G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233313289 | |||||||
| chr2:233313383 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.76-2692G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233313383 | |||||||
| chr2:233313457 | G | A | 2 | a0003c0004t0001g0318 a0003c0004t0001g0319 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.76-2618G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233313457 | |||||||
| chr2:233313515 | A | AT | 62 | a0001c0001t0001g0019 a0001c0001t0001g0064 a0001c0001t0001g0065 others(59): Show |
64 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.76-2547dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233313515 | ||||||
| chr2:233313715 | CT | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(115): Show |
126 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.76-2337delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233313715 | ||||||
| chr2:233313715 | CTT | C | 169 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(166): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.76-2338_76-2337del others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233313715 | ||||||
| chr2:233313715 | CTTT | C | 56 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0077 others(53): Show |
59 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.76-2339_76-2337del others(3): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233313715 | ||||||
| chr2:233313719 | T | G | 1 | a0002c0002t0001g0110 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.76-2356T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233313719 | |||||||
| chr2:233313809 | T | C | 3 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0002c0002t0001g0127 |
3 | HG01346.hp2 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.76-2266T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233313809 | |||||||
| chr2:233314040 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.76-2035C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233314040 | |||||||
| chr2:233314221 | C | CA | 51 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0077 others(48): Show |
54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.76-1839dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233314221 | ||||||
| chr2:233314221 | C | CAAA | 17 | a0001c0006t0001g0121 a0001c0006t0001g0122 a0001c0006t0001g0279 others(14): Show |
18 | HG02258.hp1 HG02922.hp1 HG02922.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-1841_76-1839dup others(3): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233314221 | ||||||
| chr2:233314221 | C | CAAAA | 9 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(6): Show |
9 | HG01109.hp2 HG02145.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-1842_76-1839dup others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233314221 | ||||||
| chr2:233314249 | G | T | 6 | a0001c0001t0001g0054 a0002c0002t0001g0059 a0002c0002t0001g0060 others(3): Show |
6 | HG00621.hp2 NA18991.hp1 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-1826G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233314249 | |||||||
| chr2:233314338 | C | T | 18 | a0001c0006t0001g0118 a0001c0006t0001g0121 a0001c0006t0001g0122 others(15): Show |
19 | HG02145.hp1 HG02258.hp1 HG02922.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-1737C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233314338 | |||||||
| chr2:233314631 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.76-1444C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233314631 | |||||||
| chr2:233314689 | T | C | 29 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(26): Show |
30 | HG01109.hp2 HG01358.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.76-1386T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233314689 | |||||||
| chr2:233314694 | C | T | 2 | a0001c0006t0001g0118 a0001c0006t0001g0292 |
2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.76-1381C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233314694 | |||||||
| chr2:233315191 | G | A | 25 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(22): Show |
25 | HG01109.hp2 HG01358.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.76-884G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315191 | |||||||
| chr2:233315191 | GTGGCTT | G | 8 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0077 others(5): Show |
9 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-882_76-877delGG others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315191 | ||||||
| chr2:233315201 | G | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0077 others(5): Show |
9 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-874G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315201 | |||||||
| chr2:233315203 | CT | C | 8 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0077 others(5): Show |
9 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-871delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315203 | |||||||
| chr2:233315234 | T | G | 2 | a0002c0007t0001g0072 a0002c0007t0001g0073 |
2 | HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.76-841T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315234 | |||||||
| chr2:233315240 | G | A | 20 | a0003c0004t0001g0006 a0003c0004t0001g0106 a0003c0004t0001g0129 others(17): Show |
21 | HG02717.hp1 HG02818.hp1 HG03130.hp2 others(18): Show |
intron_variant | MODIFIER | c.76-835G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315240 | |||||||
| chr2:233315281 | C | CT | 44 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0269 others(41): Show |
44 | HG00423.hp1 HG00621.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.76-765dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315281 | ||||||
| chr2:233315281 | C | CTT | 10 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0347 others(7): Show |
10 | HG01891.hp2 HG03225.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-766_76-765dupTT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315281 | ||||||
| chr2:233315281 | CT | C | 119 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(116): Show |
124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.76-765delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315281 | ||||||
| chr2:233315281 | CTT | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0066 others(5): Show |
8 | HG00639.hp2 HG01496.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-766_76-765delTT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315281 | ||||||
| chr2:233315281 | CTTTTTTT others(2): Show |
C | 31 | a0001c0003t0001g0004 a0001c0003t0001g0079 a0001c0003t0001g0081 others(28): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.76-773_76-765delTT others(7): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315281 | ||||||
| chr2:233315281 | CTTTTTTT others(9): Show |
C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0104 others(8): Show |
13 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-780_76-765delTT others(14): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315281 | ||||||
| chr2:233315411 | A | G | 1 | a0001c0003t0001g0317 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.76-664A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315411 | |||||||
| chr2:233315481 | C | T | 34 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(31): Show |
34 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.76-594C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315481 | |||||||
| chr2:233315500 | C | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0077 others(6): Show |
10 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-575C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315500 | |||||||
| chr2:233315706 | C | CT | 31 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0077 others(28): Show |
33 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-355dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315706 | ||||||
| chr2:233315726 | G | A | 1 | a0001c0001t0001g0314 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.76-349G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315726 | |||||||
| chr2:233315740 | T | C | 8 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(5): Show |
8 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-335T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315740 | |||||||
| chr2:233315744 | C | T | 5 | a0002c0002t0001g0124 a0002c0002t0001g0181 a0002c0002t0001g0182 others(2): Show |
5 | HG00733.hp1 HG00741.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-331C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315744 | |||||||
| chr2:233315809 | T | A | 1 | a0001c0001t0001g0345 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.76-266T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315809 | |||||||
| chr2:233315826 | T | C | 152 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(149): Show |
161 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.76-249T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315826 | |||||||
| chr2:233315989 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.76-86C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315989 | |||||||
| chr2:233315991 | C | T | 14 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(11): Show |
14 | HG00140.hp1 HG00280.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.76-84C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315991 | |||||||
| chr2:233315997 | G | C | 37 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(34): Show |
37 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.76-78G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315997 | |||||||
| chr2:233316004 | GCTGGTTT others(13): Show |
G | 2 | a0001c0006t0001g0118 a0001c0006t0001g0292 |
2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.76-68_76-49delGGTT others(16): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233316004 | ||||||
| chr2:233316035 | C | T | 17 | a0003c0004t0001g0106 a0003c0004t0001g0129 a0003c0004t0001g0131 others(14): Show |
17 | HG03239.hp1 HG03490.hp2 HG03579.hp1 others(14): Show |
intron_variant | MODIFIER | c.76-40C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233316035 | |||||||
| chr2:233316048 | T | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.76-27T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233316048 | |||||||
| chr2:233316239 | G | A | 1 | a0002c0002t0001g0323 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.136+104G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233316239 | |||||||
| chr2:233316380 | T | C | 6 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(3): Show |
6 | NA18941.hp2 NA18942.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+245T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233316380 | |||||||
| chr2:233316557 | C | T | 4 | a0001c0006t0001g0286 a0002c0009t0001g0280 a0002c0009t0001g0288 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+422C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233316557 | |||||||
| chr2:233316581 | G | A | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(15): Show |
20 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.136+446G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233316581 | |||||||
| chr2:233316622 | T | C | 1 | a0002c0009t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.136+487T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233316622 | |||||||
| chr2:233317018 | C | T | 1 | a0002c0002t0001g0177 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.136+883C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317018 | |||||||
| chr2:233317035 | T | C | 69 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(66): Show |
70 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(67): Show |
intron_variant | MODIFIER | c.136+900T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317035 | |||||||
| chr2:233317217 | C | T | 31 | a0001c0006t0001g0118 a0001c0006t0001g0286 a0001c0006t0001g0292 others(28): Show |
32 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.136+1082C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317217 | |||||||
| chr2:233317394 | T | C | 4 | a0001c0006t0001g0121 a0001c0006t0001g0122 a0001c0006t0001g0279 others(1): Show |
5 | HG02922.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+1259T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317394 | |||||||
| chr2:233317396 | G | A | 1 | a0002c0007t0001g0080 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.136+1261G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317396 | |||||||
| chr2:233317484 | C | T | 6 | a0001c0006t0001g0118 a0001c0006t0001g0286 a0001c0006t0001g0292 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-1267C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317484 | |||||||
| chr2:233317655 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.137-1096G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317655 | |||||||
| chr2:233317689 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.137-1062G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317689 | |||||||
| chr2:233317714 | T | C | 4 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(1): Show |
4 | HG00140.hp1 HG00280.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-1037T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317714 | |||||||
| chr2:233317723 | A | T | 3 | a0003c0004t0001g0129 a0003c0004t0001g0141 a0003c0004t0001g0295 |
3 | NA18967.hp1 NA18977.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.137-1028A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317723 | |||||||
| chr2:233317793 | CTA | C | 5 | a0002c0005t0001g0283 a0002c0005t0001g0284 a0002c0007t0001g0072 others(2): Show |
5 | HG02965.hp1 HG02965.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-954_137-953del others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 233317793 | ||||||
| chr2:233317830 | T | C | 1 | a0001c0001t0003g0215 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.137-921T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317830 | |||||||
| chr2:233317924 | C | A | 1 | a0002c0002t0001g0200 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.137-827C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317924 | |||||||
| chr2:233317945 | G | A | 6 | a0001c0006t0001g0118 a0001c0006t0001g0286 a0001c0006t0001g0292 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-806G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317945 | |||||||
| chr2:233318074 | G | A | 238 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(235): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.137-677G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318074 | |||||||
| chr2:233318128 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.137-623C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318128 | |||||||
| chr2:233318133 | C | T | 11 | a0001c0003t0001g0337 a0002c0002t0001g0016 a0002c0002t0001g0331 others(8): Show |
12 | HG00673.hp1 HG02040.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.137-618C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318133 | |||||||
| chr2:233318208 | A | G | 11 | a0001c0006t0001g0118 a0001c0006t0001g0121 a0001c0006t0001g0122 others(8): Show |
12 | HG02145.hp1 HG02258.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.137-543A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318208 | |||||||
| chr2:233318243 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.137-508C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318243 | |||||||
| chr2:233318296 | T | C | 4 | a0001c0006t0001g0121 a0001c0006t0001g0122 a0001c0006t0001g0279 others(1): Show |
5 | HG02922.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-455T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318296 | |||||||
| chr2:233318331 | A | AT | 26 | a0002c0002t0001g0115 a0002c0002t0001g0176 a0003c0004t0001g0006 others(23): Show |
27 | HG02055.hp1 HG02155.hp2 HG02572.hp2 others(24): Show |
intron_variant | MODIFIER | c.137-408dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 233318331 | ||||||
| chr2:233318341 | T | G | 14 | a0001c0001t0001g0218 a0001c0006t0001g0118 a0001c0006t0001g0121 others(11): Show |
15 | HG00438.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.137-410T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318341 | |||||||
| chr2:233318401 | T | A | 151 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0148 others(148): Show |
159 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.137-350T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318401 | |||||||
| chr2:233318453 | G | T | 2 | a0002c0007t0001g0072 a0002c0007t0001g0073 |
2 | HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.137-298G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318453 | |||||||
| chr2:233318467 | G | C | 35 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0006t0001g0121 others(32): Show |
37 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.137-284G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318467 | |||||||
| chr2:233318472 | G | A | 38 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(35): Show |
38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.137-279G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318472 | |||||||
| chr2:233318820 | G | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0104 others(8): Show |
13 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.181+25G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233318820 | |||||||
| chr2:233318834 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | NA18952.hp2 NA18956.hp1 NA19001.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+39G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233318834 | |||||||
| chr2:233318877 | A | G | 239 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(236): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.181+82A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233318877 | |||||||
| chr2:233319047 | C | T | 96 | a0001c0001t0001g0148 a0001c0001t0001g0154 a0001c0001t0001g0159 others(93): Show |
102 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.181+252C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319047 | |||||||
| chr2:233319048 | G | A | 1 | a0001c0003t0001g0317 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.181+253G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319048 | |||||||
| chr2:233319053 | C | T | 36 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0006t0001g0118 others(33): Show |
37 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.181+258C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319053 | |||||||
| chr2:233319065 | C | G | 10 | a0001c0006t0001g0118 a0001c0006t0001g0121 a0001c0006t0001g0122 others(7): Show |
10 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.181+270C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319065 | |||||||
| chr2:233319067 | C | T | 10 | a0001c0006t0001g0118 a0001c0006t0001g0121 a0001c0006t0001g0122 others(7): Show |
10 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.181+272C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319067 | |||||||
| chr2:233319290 | T | TG | 241 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(238): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.181+500dupG | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 233319290 | ||||||
| chr2:233319359 | G | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0104 others(8): Show |
13 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.181+564G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319359 | |||||||
| chr2:233319584 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.181+789G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319584 | |||||||
| chr2:233319591 | G | GA | 132 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(129): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.181+796_181+797ins others(1): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319591 | |||||||
| chr2:233319848 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.182-782C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319848 | |||||||
| chr2:233319928 | C | T | 1 | a0002c0005t0001g0301 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.182-702C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319928 | |||||||
| chr2:233319957 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.182-673C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319957 | |||||||
| chr2:233320012 | C | A | 11 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0058 others(8): Show |
11 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.182-618C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320012 | |||||||
| chr2:233320012 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.182-618C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320012 | |||||||
| chr2:233320091 | G | A | 2 | a0001c0003t0001g0290 a0001c0003t0001g0291 |
2 | HG00323.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.182-539G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320091 | |||||||
| chr2:233320284 | C | A | 1 | a0001c0001t0001g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.182-346C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320284 | |||||||
| chr2:233320300 | A | G | 24 | a0003c0004t0001g0006 a0003c0004t0001g0106 a0003c0004t0001g0129 others(21): Show |
25 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(22): Show |
intron_variant | MODIFIER | c.182-330A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320300 | |||||||
| chr2:233320339 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0103 a0001c0001t0001g0219 |
3 | HG01361.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.182-291G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320339 | |||||||
| chr2:233320437 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.182-193C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320437 | |||||||
| chr2:233320454 | G | C | 1 | a0002c0002t0001g0324 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.182-176G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320454 | |||||||
| chr2:233320556 | G | A | 2 | a0002c0002t0001g0150 a0002c0002t0001g0151 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.182-74G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320556 | |||||||
| chr2:233320568 | G | A | 11 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0058 others(8): Show |
11 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.182-62G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320568 | |||||||
| chr2:233320617 | A | G | 1 | a0002c0007t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.182-13A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320617 | |||||||
| chr2:233320834 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0037 others(2): Show |
5 | HG01168.hp1 HG01255.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.375+11C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233320834 | |||||||
| chr2:233320892 | G | GGAAAGGG others(9): Show |
1 | a0003c0004t0001g0131 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.375+76_375+77insAT others(14): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233320892 | ||||||
| chr2:233320915 | T | C | 2 | a0001c0006t0001g0118 a0001c0006t0001g0292 |
2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.375+92T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233320915 | |||||||
| chr2:233321012 | C | G | 1 | a0001c0001t0001g0254 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.375+189C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321012 | |||||||
| chr2:233321280 | T | G | 32 | a0001c0003t0001g0004 a0001c0003t0001g0079 a0001c0003t0001g0081 others(29): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.375+457T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321280 | |||||||
| chr2:233321307 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.375+484C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321307 | |||||||
| chr2:233321308 | G | A | 1 | a0002c0009t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.375+485G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321308 | |||||||
| chr2:233321520 | C | G | 1 | a0003c0004t0001g0129 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.375+697C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321520 | |||||||
| chr2:233321888 | G | A | 9 | a0001c0006t0001g0118 a0001c0006t0001g0121 a0001c0006t0001g0122 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.376-1058G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321888 | |||||||
| chr2:233321914 | C | T | 2 | a0002c0002t0001g0329 a0002c0002t0001g0330 |
2 | HG00558.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.376-1032C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321914 | |||||||
| chr2:233321950 | T | C | 63 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(60): Show |
64 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.376-996T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321950 | |||||||
| chr2:233321986 | T | TAC | 19 | a0001c0001t0001g0054 a0001c0001t0001g0195 a0001c0001t0001g0212 others(16): Show |
20 | HG00735.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.376-910_376-909dup others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | ||||||
| chr2:233321986 | T | TACAC | 12 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0128 others(9): Show |
13 | HG00621.hp1 HG01358.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.376-912_376-909dup others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | ||||||
| chr2:233321986 | TAC | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0103 others(37): Show |
44 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.376-910_376-909del others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | ||||||
| chr2:233321986 | TACAC | T | 30 | a0001c0001t0001g0109 a0001c0001t0001g0119 a0001c0001t0001g0243 others(27): Show |
30 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.376-912_376-909del others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | ||||||
| chr2:233321986 | TACACAC | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0203 a0001c0001t0001g0250 others(11): Show |
16 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.376-914_376-909del others(6): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | ||||||
| chr2:233321986 | TACACACA others(1): Show |
T | 11 | a0001c0001t0001g0251 a0001c0001t0001g0347 a0001c0003t0003g0086 others(8): Show |
11 | HG00609.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.376-916_376-909del others(8): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | ||||||
| chr2:233321986 | TACACACA others(3): Show |
T | 5 | a0001c0003t0001g0093 a0002c0002t0001g0326 a0002c0002t0001g0327 others(2): Show |
5 | HG00280.hp2 HG02965.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.376-918_376-909del others(10): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | ||||||
| chr2:233321986 | TACACACA others(5): Show |
T | 11 | a0001c0001t0001g0154 a0001c0003t0001g0317 a0001c0003t0003g0258 others(8): Show |
11 | HG01358.hp2 HG01978.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.376-920_376-909del others(12): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | ||||||
| chr2:233321986 | TACACACA others(7): Show |
T | 83 | a0001c0001t0001g0148 a0001c0001t0001g0159 a0001c0001t0001g0164 others(80): Show |
89 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.376-922_376-909del others(14): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | ||||||
| chr2:233321986 | TACACACA others(9): Show |
T | 3 | a0002c0002t0001g0150 a0002c0002t0001g0151 a0002c0002t0001g0172 |
3 | HG00280.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.376-924_376-909del others(16): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | ||||||
| chr2:233321986 | TACACACA others(11): Show |
T | 24 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0252 others(21): Show |
25 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.376-926_376-909del others(18): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | ||||||
| chr2:233321986 | TACACACA others(13): Show |
T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(14): Show |
19 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.376-928_376-909del others(20): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | ||||||
| chr2:233321986 | TACACACA others(15): Show |
T | 40 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(37): Show |
40 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.376-930_376-909del others(22): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | ||||||
| chr2:233322026 | C | T | 2 | a0002c0002t0001g0173 a0002c0002t0001g0174 |
2 | HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.376-920C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322026 | |||||||
| chr2:233322030 | C | T | 1 | a0002c0002t0001g0114 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.376-916C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322030 | |||||||
| chr2:233322038 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.376-908T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322038 | |||||||
| chr2:233322055 | C | T | 1 | a0002c0002t0001g0056 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.376-891C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322055 | |||||||
| chr2:233322111 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.376-835C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322111 | |||||||
| chr2:233322173 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0103 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.376-773G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322173 | |||||||
| chr2:233322185 | C | CA | 31 | a0001c0001t0001g0014 a0001c0001t0001g0070 a0001c0001t0001g0104 others(28): Show |
32 | HG00733.hp1 HG00741.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.376-737dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233322185 | ||||||
| chr2:233322185 | CA | C | 64 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(61): Show |
65 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.376-737delA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233322185 | ||||||
| chr2:233322185 | CAA | C | 14 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0293 others(11): Show |
14 | HG01081.hp2 HG01256.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.376-738_376-737del others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233322185 | ||||||
| chr2:233322185 | CAAA | C | 18 | a0001c0003t0001g0004 a0001c0003t0001g0079 a0001c0003t0001g0081 others(15): Show |
19 | HG00738.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.376-739_376-737del others(3): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233322185 | ||||||
| chr2:233322185 | CAAAA | C | 6 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(3): Show |
6 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-740_376-737del others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233322185 | ||||||
| chr2:233322332 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.376-614C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322332 | |||||||
| chr2:233322372 | G | C | 94 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(91): Show |
96 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.376-574G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322372 | |||||||
| chr2:233322392 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.376-554G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322392 | |||||||
| chr2:233322406 | A | T | 1 | a0003c0004t0001g0131 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-540A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322406 | |||||||
| chr2:233322409 | C | A | 1 | a0003c0004t0001g0131 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-537C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322409 | |||||||
| chr2:233322410 | T | A | 1 | a0003c0004t0001g0131 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-536T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322410 | |||||||
| chr2:233322412 | T | G | 1 | a0003c0004t0001g0131 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-534T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322412 | |||||||
| chr2:233322413 | C | A | 1 | a0003c0004t0001g0131 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-533C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322413 | |||||||
| chr2:233322416 | A | T | 1 | a0003c0004t0001g0131 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-530A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322416 | |||||||
| chr2:233322417 | A | G | 1 | a0003c0004t0001g0131 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-529A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322417 | |||||||
| chr2:233322608 | C | T | 1 | a0003c0004t0001g0131 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-338C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322608 | |||||||
| chr2:233322610 | G | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0002c0005t0001g0005 others(8): Show |
12 | HG02647.hp2 HG02922.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.376-336G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322610 | |||||||
| chr2:233322681 | A | G | 1 | a0003c0004t0001g0131 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-265A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322681 | |||||||
| chr2:233322688 | C | A | 29 | a0001c0003t0001g0004 a0001c0003t0001g0079 a0001c0003t0001g0081 others(26): Show |
30 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.376-258C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322688 | |||||||
| chr2:233322702 | T | A | 1 | a0003c0004t0001g0131 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-244T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322702 | |||||||
| chr2:233322703 | C | T | 1 | a0003c0004t0001g0131 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-243C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322703 | |||||||
| chr2:233322707 | C | A | 1 | a0003c0004t0001g0131 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-239C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322707 | |||||||
| chr2:233322755 | A | G | 4 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(1): Show |
4 | HG00140.hp1 HG00280.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-191A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322755 | |||||||
| chr2:233322796 | T | G | 1 | a0001c0001t0001g0273 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.376-150T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322796 | |||||||
| chr2:233323110 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.435+105G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233323110 | |||||||
| chr2:233323380 | T | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0104 others(8): Show |
13 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.435+375T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233323380 | |||||||
| chr2:233323382 | A | T | 1 | a0001c0001t0001g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.435+377A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233323382 | |||||||
| chr2:233323675 | A | C | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.435+670A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233323675 | |||||||
| chr2:233323750 | C | A | 1 | a0002c0002t0001g0332 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.435+745C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233323750 | |||||||
| chr2:233323765 | C | T | 2 | a0001c0001t0001g0239 a0001c0001t0001g0270 |
2 | NA18992.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.435+760C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233323765 | |||||||
| chr2:233323813 | C | T | 1 | a0002c0009t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.435+808C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233323813 | |||||||
| chr2:233324076 | T | G | 157 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(154): Show |
164 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.435+1071T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324076 | |||||||
| chr2:233324213 | G | A | 1 | a0003c0004t0001g0006 | 2 | HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.435+1208G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324213 | |||||||
| chr2:233324274 | A | C | 241 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(238): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.435+1269A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324274 | |||||||
| chr2:233324373 | A | G | 63 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(60): Show |
64 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.435+1368A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324373 | |||||||
| chr2:233324420 | A | C | 38 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(35): Show |
38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.435+1415A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324420 | |||||||
| chr2:233324584 | G | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0043 a0001c0001t0001g0046 others(1): Show |
4 | HG00423.hp2 HG02080.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1579G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324584 | |||||||
| chr2:233324589 | C | G | 241 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(238): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.435+1584C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324589 | |||||||
| chr2:233324601 | G | A | 1 | a0002c0002t0001g0059 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.435+1596G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324601 | |||||||
| chr2:233324607 | G | A | 1 | a0002c0002t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.435+1602G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324607 | |||||||
| chr2:233324609 | A | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0043 a0001c0001t0001g0046 others(1): Show |
4 | HG00423.hp2 HG02080.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1604A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324609 | |||||||
| chr2:233324681 | C | T | 9 | a0001c0006t0001g0118 a0001c0006t0001g0121 a0001c0006t0001g0122 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.435+1676C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324681 | |||||||
| chr2:233324682 | G | A | 1 | a0002c0009t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.435+1677G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324682 | |||||||
| chr2:233324711 | G | C | 1 | a0001c0003t0001g0099 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.435+1706G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324711 | |||||||
| chr2:233324845 | G | A | 178 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(175): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.435+1840G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324845 | |||||||
| chr2:233324870 | G | A | 59 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(56): Show |
62 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.435+1865G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324870 | |||||||
| chr2:233324947 | A | T | 38 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(35): Show |
38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.435+1942A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324947 | |||||||
| chr2:233324968 | G | A | 3 | a0001c0006t0001g0121 a0001c0006t0001g0122 a0001c0006t0001g0279 |
3 | HG03130.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.435+1963G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324968 | |||||||
| chr2:233325019 | A | G | 1 | a0002c0009t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.435+2014A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325019 | |||||||
| chr2:233325095 | G | A | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.436-2026G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325095 | |||||||
| chr2:233325203 | C | CA | 26 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(23): Show |
28 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.436-1900dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233325203 | ||||||
| chr2:233325203 | C | CAA | 23 | a0002c0009t0001g0078 a0003c0004t0001g0006 a0003c0004t0001g0106 others(20): Show |
24 | HG02572.hp2 HG02818.hp1 HG02896.hp1 others(21): Show |
intron_variant | MODIFIER | c.436-1901_436-1900d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233325203 | ||||||
| chr2:233325203 | CA | C | 101 | a0001c0001t0001g0148 a0001c0001t0001g0154 a0001c0001t0001g0164 others(98): Show |
107 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.436-1900delA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233325203 | ||||||
| chr2:233325237 | A | G | 38 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(35): Show |
38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.436-1884A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325237 | |||||||
| chr2:233325299 | T | C | 3 | a0001c0001t0001g0233 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | NA18948.hp1 NA19056.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.436-1822T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325299 | |||||||
| chr2:233325351 | A | G | 1 | a0002c0009t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.436-1770A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325351 | |||||||
| chr2:233325354 | T | TA | 145 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(142): Show |
154 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.436-1752dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233325354 | ||||||
| chr2:233325354 | T | TAA | 27 | a0001c0001t0001g0018 a0001c0001t0001g0293 a0002c0002t0001g0186 others(24): Show |
28 | HG01256.hp1 HG02055.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.436-1753_436-1752d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233325354 | ||||||
| chr2:233325354 | T | TAAA | 36 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(33): Show |
36 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.436-1754_436-1752d others(5): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233325354 | ||||||
| chr2:233325458 | C | CAT | 241 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(238): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.436-1663_436-1662i others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325458 | |||||||
| chr2:233325546 | C | T | 5 | a0002c0005t0001g0281 a0002c0005t0001g0282 a0002c0005t0001g0287 others(2): Show |
5 | HG03453.hp1 HG03486.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-1575C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325546 | |||||||
| chr2:233325730 | G | A | 32 | a0001c0003t0001g0004 a0001c0003t0001g0079 a0001c0003t0001g0081 others(29): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.436-1391G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325730 | |||||||
| chr2:233325785 | C | T | 25 | a0002c0009t0001g0078 a0003c0004t0001g0006 a0003c0004t0001g0106 others(22): Show |
26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.436-1336C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325785 | |||||||
| chr2:233325892 | C | G | 39 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(36): Show |
39 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.436-1229C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325892 | |||||||
| chr2:233325898 | C | T | 1 | a0002c0009t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.436-1223C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325898 | |||||||
| chr2:233325980 | A | G | 241 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(238): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.436-1141A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325980 | |||||||
| chr2:233326009 | GA | G | 38 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(35): Show |
38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.436-1111delA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326009 | |||||||
| chr2:233326033 | T | C | 25 | a0002c0009t0001g0078 a0003c0004t0001g0006 a0003c0004t0001g0106 others(22): Show |
26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.436-1088T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326033 | |||||||
| chr2:233326069 | G | A | 1 | a0002c0002t0001g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.436-1052G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326069 | |||||||
| chr2:233326077 | C | T | 3 | a0001c0003t0001g0337 a0002c0007t0001g0072 a0002c0007t0001g0073 |
3 | HG02129.hp2 HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.436-1044C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326077 | |||||||
| chr2:233326090 | T | C | 2 | a0007c0017t0001g0299 a0009c0018t0001g0191 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.436-1031T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326090 | |||||||
| chr2:233326112 | G | A | 183 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(180): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.436-1009G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326112 | |||||||
| chr2:233326182 | G | A | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.436-939G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326182 | |||||||
| chr2:233326199 | C | G | 242 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(239): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.436-922C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326199 | |||||||
| chr2:233326210 | G | A | 38 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(35): Show |
38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.436-911G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326210 | |||||||
| chr2:233326276 | C | T | 38 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(35): Show |
38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.436-845C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326276 | |||||||
| chr2:233326313 | G | A | 96 | a0001c0001t0001g0148 a0001c0001t0001g0154 a0001c0001t0001g0159 others(93): Show |
102 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.436-808G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326313 | |||||||
| chr2:233326418 | C | T | 119 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0148 others(116): Show |
126 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.436-703C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326418 | |||||||
| chr2:233326508 | T | C | 242 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(239): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.436-613T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326508 | |||||||
| chr2:233326533 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | NA18948.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.436-588C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326533 | |||||||
| chr2:233326584 | T | G | 1 | a0002c0009t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.436-537T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326584 | |||||||
| chr2:233326586 | C | CA | 52 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0027 others(49): Show |
53 | HG00438.hp1 HG00741.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.436-517dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233326586 | ||||||
| chr2:233326586 | C | CAA | 6 | a0003c0004t0001g0131 a0003c0004t0001g0132 a0003c0004t0001g0142 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.436-518_436-517dup others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233326586 | ||||||
| chr2:233326586 | CA | C | 6 | a0001c0001t0001g0066 a0001c0001t0001g0189 a0001c0003t0001g0101 others(3): Show |
6 | HG02129.hp2 HG02572.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-517delA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233326586 | ||||||
| chr2:233326616 | G | T | 33 | a0001c0003t0001g0004 a0001c0003t0001g0079 a0001c0003t0001g0081 others(30): Show |
34 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.436-505G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326616 | |||||||
| chr2:233326656 | T | C | 25 | a0002c0009t0001g0078 a0003c0004t0001g0006 a0003c0004t0001g0106 others(22): Show |
26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.436-465T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326656 | |||||||
| chr2:233326697 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.436-424A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326697 | |||||||
| chr2:233326714 | C | A | 119 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0148 others(116): Show |
126 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.436-407C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326714 | |||||||
| chr2:233326808 | A | G | 38 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(35): Show |
38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.436-313A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326808 | |||||||
| chr2:233326824 | A | G | 242 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(239): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.436-297A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326824 | |||||||
| chr2:233326898 | C | CT | 8 | a0002c0005t0001g0281 a0002c0005t0001g0282 a0002c0005t0001g0283 others(5): Show |
8 | HG02965.hp1 HG03453.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.436-223_436-222ins others(1): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326898 | |||||||
| chr2:233327085 | G | A | 1 | a0002c0002t0001g0177 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.436-36G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233327085 | |||||||
| chr2:233327091 | C | T | 1 | a0002c0005t0001g0298 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.436-30C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233327091 | |||||||
| chr2:233327103 | G | C | 119 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0148 others(116): Show |
126 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.436-18G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233327103 | |||||||
| chr2:233327255 | C | G | 1 | a0001c0001t0001g0211 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.512+58C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327255 | |||||||
| chr2:233327255 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.512+58C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327255 | |||||||
| chr2:233327434 | G | A | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(15): Show |
20 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.512+237G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327434 | |||||||
| chr2:233327464 | G | GTTGT | 40 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(37): Show |
40 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.512+290_512+293dup others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 233327464 | ||||||
| chr2:233327464 | GTTGT | G | 5 | a0002c0005t0001g0281 a0002c0005t0001g0282 a0002c0005t0001g0287 others(2): Show |
5 | HG03453.hp1 HG03486.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.512+290_512+293del others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 233327464 | ||||||
| chr2:233327535 | C | CT | 24 | a0003c0004t0001g0006 a0003c0004t0001g0106 a0003c0004t0001g0129 others(21): Show |
25 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(22): Show |
intron_variant | MODIFIER | c.512+346dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 233327535 | ||||||
| chr2:233327535 | C | T | 1 | a0002c0009t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.512+338C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327535 | |||||||
| chr2:233327550 | T | C | 25 | a0002c0009t0001g0078 a0003c0004t0001g0006 a0003c0004t0001g0106 others(22): Show |
26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.512+353T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327550 | |||||||
| chr2:233327551 | T | A | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(57): Show |
63 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.512+354T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327551 | |||||||
| chr2:233327580 | C | T | 1 | a0001c0001t0006g0296 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.512+383C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327580 | |||||||
| chr2:233327612 | G | A | 1 | a0001c0003t0001g0317 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.512+415G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327612 | |||||||
| chr2:233327657 | C | A | 2 | a0001c0003t0001g0337 a0002c0007t0001g0072 |
2 | HG02129.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.512+460C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327657 | |||||||
| chr2:233327688 | G | A | 3 | a0001c0006t0001g0121 a0001c0006t0001g0122 a0001c0006t0001g0279 |
3 | HG03130.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.512+491G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327688 | |||||||
| chr2:233327709 | A | AT | 48 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(45): Show |
51 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(48): Show |
intron_variant | MODIFIER | c.512+525dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 233327709 | ||||||
| chr2:233327750 | A | G | 1 | a0002c0002t0001g0201 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.512+553A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327750 | |||||||
| chr2:233327781 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.512+584C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327781 | |||||||
| chr2:233327868 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.513-610A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327868 | |||||||
| chr2:233328015 | GT | G | 26 | a0001c0006t0001g0121 a0002c0009t0001g0078 a0003c0004t0001g0006 others(23): Show |
27 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(24): Show |
intron_variant | MODIFIER | c.513-453delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 233328015 | ||||||
| chr2:233328042 | C | T | 25 | a0002c0009t0001g0078 a0003c0004t0001g0006 a0003c0004t0001g0106 others(22): Show |
26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.513-436C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328042 | |||||||
| chr2:233328054 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.513-424C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328054 | |||||||
| chr2:233328065 | C | T | 1 | a0002c0002t0001g0112 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.513-413C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328065 | |||||||
| chr2:233328067 | T | C | 123 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0020 others(120): Show |
127 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.513-411T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328067 | |||||||
| chr2:233328076 | T | C | 25 | a0002c0009t0001g0078 a0003c0004t0001g0006 a0003c0004t0001g0106 others(22): Show |
26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.513-402T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328076 | |||||||
| chr2:233328208 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.513-270C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328208 | |||||||
| chr2:233328215 | T | C | 98 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0020 others(95): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.513-263T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328215 | |||||||
| chr2:233328251 | C | T | 2 | a0003c0004t0001g0318 a0003c0004t0001g0319 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.513-227C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328251 | |||||||
| chr2:233328299 | C | T | 1 | a0002c0002t0001g0112 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.513-179C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328299 | |||||||
| chr2:233328305 | C | T | 25 | a0002c0009t0001g0078 a0003c0004t0001g0006 a0003c0004t0001g0106 others(22): Show |
26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.513-173C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328305 | |||||||
| chr2:233328309 | G | A | 25 | a0002c0009t0001g0078 a0003c0004t0001g0006 a0003c0004t0001g0106 others(22): Show |
26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.513-169G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328309 | |||||||
| chr2:233328319 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.513-159C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328319 | |||||||
| chr2:233328340 | G | C | 25 | a0002c0009t0001g0078 a0003c0004t0001g0006 a0003c0004t0001g0106 others(22): Show |
26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.513-138G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328340 | |||||||
| chr2:233328357 | C | A | 1 | a0001c0001t0001g0270 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.513-121C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328357 | |||||||
| chr2:233328402 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.513-76A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328402 | |||||||
| chr2:233328671 | A | T | 1 | a0002c0002t0001g0112 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.648+58A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 8/15 | chr2 | 233328671 | |||||||
| chr2:233328741 | A | G | 120 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0148 others(117): Show |
127 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.648+128A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 8/15 | chr2 | 233328741 | |||||||
| chr2:233328813 | C | T | 1 | a0002c0009t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.648+200C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 8/15 | chr2 | 233328813 | |||||||
| chr2:233329119 | T | G | 242 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(239): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.649-374T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 8/15 | chr2 | 233329119 | |||||||
| chr2:233329254 | AC | A | 7 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(4): Show |
7 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.649-235delC | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 233329254 | ||||||
| chr2:233329608 | T | G | 242 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(239): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.733+31T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233329608 | |||||||
| chr2:233329724 | C | T | 1 | a0001c0001t0001g0314 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.733+147C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233329724 | |||||||
| chr2:233329725 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0303 |
2 | HG02155.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.733+148G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233329725 | |||||||
| chr2:233329775 | C | A | 1 | a0002c0002t0001g0331 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.733+198C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233329775 | |||||||
| chr2:233329791 | T | A | 1 | a0002c0002t0001g0112 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.733+214T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233329791 | |||||||
| chr2:233329936 | A | G | 7 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(4): Show |
7 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.733+359A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233329936 | |||||||
| chr2:233330013 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.733+436G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330013 | |||||||
| chr2:233330038 | G | T | 1 | a0001c0003t0001g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.733+461G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330038 | |||||||
| chr2:233330138 | A | G | 242 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(239): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.733+561A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330138 | |||||||
| chr2:233330254 | A | G | 242 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(239): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.733+677A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330254 | |||||||
| chr2:233330303 | G | A | 15 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(12): Show |
15 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.733+726G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330303 | |||||||
| chr2:233330426 | A | G | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(15): Show |
20 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.733+849A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330426 | |||||||
| chr2:233330465 | TTCCC | T | 41 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0052 others(38): Show |
42 | HG00642.hp1 HG00741.hp2 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.733+898_733+901del others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330465 | ||||||
| chr2:233330471 | C | CCCTT | 3 | a0001c0003t0001g0101 a0001c0019t0001g0169 a0002c0005t0001g0039 |
3 | HG01106.hp2 HG03579.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.733+897_733+898ins others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330471 | ||||||
| chr2:233330471 | CCCTCCCT others(1): Show |
C | 77 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0026 others(74): Show |
81 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+898_733+905del others(8): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330471 | ||||||
| chr2:233330471 | CCCTCCCT others(5): Show |
C | 62 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0022 others(59): Show |
63 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.733+898_733+909del others(12): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330471 | ||||||
| chr2:233330471 | CCCTCCCT others(9): Show |
C | 23 | a0001c0001t0001g0037 a0001c0001t0001g0260 a0001c0001t0007g0069 others(20): Show |
25 | HG00140.hp2 HG00558.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.733+898_733+913del others(16): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330471 | ||||||
| chr2:233330471 | CCCTCCCT others(13): Show |
C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0050 others(3): Show |
6 | HG02109.hp1 HG02615.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.733+898_733+917del others(20): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330471 | ||||||
| chr2:233330471 | CCCTCCCT others(17): Show |
C | 3 | a0001c0001t0001g0049 a0001c0001t0001g0053 a0001c0003t0001g0317 |
3 | HG01358.hp2 HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.733+898_733+921del others(24): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330471 | ||||||
| chr2:233330471 | CCCTCCCT others(25): Show |
C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0051 |
2 | NA18947.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.733+898_733+929del others(32): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330471 | ||||||
| chr2:233330475 | C | CCCTT | 14 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0019 others(11): Show |
15 | HG01099.hp2 HG01257.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.733+962_733+965dup others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330475 | ||||||
| chr2:233330475 | C | T | 17 | a0001c0001t0001g0044 a0001c0001t0001g0066 a0001c0001t0001g0067 others(14): Show |
18 | HG01106.hp2 HG01978.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.733+898C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330475 | |||||||
| chr2:233330475 | CCCTT | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0014 others(50): Show |
53 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.733+962_733+965del others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330475 | ||||||
| chr2:233330475 | CCCTTCCT others(1): Show |
C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0074 others(26): Show |
29 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.733+958_733+965del others(8): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330475 | ||||||
| chr2:233330475 | CCCTTCCT others(5): Show |
C | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0107 others(6): Show |
10 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.733+954_733+965del others(12): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330475 | ||||||
| chr2:233330475 | CCCTTCCT others(9): Show |
C | 1 | a0001c0001t0001g0001 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.733+950_733+965del others(16): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330475 | ||||||
| chr2:233330479 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0303 |
2 | HG03225.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.733+902T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330479 | |||||||
| chr2:233330483 | T | C | 5 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0001t0002g0197 others(2): Show |
5 | HG00735.hp2 HG01192.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.733+906T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330483 | |||||||
| chr2:233330487 | T | C | 4 | a0001c0001t0001g0240 a0001c0001t0002g0179 a0001c0001t0002g0224 others(1): Show |
4 | HG01168.hp2 HG01943.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+910T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330487 | |||||||
| chr2:233330491 | T | C | 1 | a0001c0001t0002g0198 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.733+914T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330491 | |||||||
| chr2:233330675 | C | T | 9 | a0001c0006t0001g0118 a0001c0006t0001g0121 a0001c0006t0001g0122 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.734-965C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330675 | |||||||
| chr2:233330781 | C | T | 5 | a0001c0003t0001g0094 a0001c0003t0001g0096 a0001c0003t0001g0097 others(2): Show |
5 | HG02257.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-859C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330781 | |||||||
| chr2:233331052 | T | G | 1 | a0002c0002t0001g0112 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.734-588T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233331052 | |||||||
| chr2:233331054 | A | T | 1 | a0002c0002t0001g0112 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.734-586A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233331054 | |||||||
| chr2:233331089 | A | G | 33 | a0001c0003t0001g0004 a0001c0003t0001g0079 a0001c0003t0001g0081 others(30): Show |
34 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.734-551A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233331089 | |||||||
| chr2:233331195 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0257 |
2 | HG00609.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.734-445C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233331195 | |||||||
| chr2:233331265 | C | T | 1 | a0002c0002t0001g0152 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.734-375C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233331265 | |||||||
| chr2:233331558 | C | T | 1 | a0001c0001t0003g0125 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.734-82C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233331558 | |||||||
| chr2:233331578 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.734-62A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233331578 | |||||||
| chr2:233331776 | G | A | 1 | a0004c0008t0001g0075 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.806+64G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233331776 | |||||||
| chr2:233331822 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0103 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.806+110C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233331822 | |||||||
| chr2:233331932 | A | T | 1 | a0002c0005t0001g0005 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.806+220A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233331932 | |||||||
| chr2:233331933 | T | C | 1 | a0002c0002t0001g0186 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.806+221T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233331933 | |||||||
| chr2:233332038 | G | A | 242 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(239): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.806+326G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233332038 | |||||||
| chr2:233332419 | T | G | 1 | a0001c0001t0001g0270 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.806+707T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233332419 | |||||||
| chr2:233332452 | A | G | 242 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(239): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.806+740A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233332452 | |||||||
| chr2:233332646 | A | C | 242 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(239): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.806+934A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233332646 | |||||||
| chr2:233332663 | A | AT | 38 | a0001c0001t0001g0193 a0001c0001t0001g0210 a0001c0001t0001g0303 others(35): Show |
39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.806+966dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 233332663 | ||||||
| chr2:233332663 | A | ATT | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0104 others(9): Show |
14 | HG02109.hp2 HG02145.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.806+965_806+966dup others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 233332663 | ||||||
| chr2:233332663 | A | ATTT | 10 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(7): Show |
10 | HG01109.hp2 HG02074.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.806+964_806+966dup others(3): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 233332663 | ||||||
| chr2:233332663 | A | ATTTT | 114 | a0001c0001t0001g0148 a0001c0001t0001g0154 a0001c0001t0001g0159 others(111): Show |
121 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.806+963_806+966dup others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 233332663 | ||||||
| chr2:233332663 | A | ATTTTT | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0002c0002t0001g0112 others(3): Show |
6 | HG01175.hp1 HG02647.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.806+962_806+966dup others(5): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 233332663 | ||||||
| chr2:233332863 | A | G | 30 | a0001c0003t0001g0004 a0001c0003t0001g0079 a0001c0003t0001g0081 others(27): Show |
31 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.806+1151A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233332863 | |||||||
| chr2:233332944 | T | C | 1 | a0002c0002t0001g0114 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.806+1232T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233332944 | |||||||
| chr2:233333016 | A | G | 38 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(35): Show |
38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.806+1304A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333016 | |||||||
| chr2:233333048 | A | G | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(15): Show |
20 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.806+1336A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333048 | |||||||
| chr2:233333116 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0051 |
3 | NA18947.hp2 NA18990.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.806+1404G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333116 | |||||||
| chr2:233333444 | C | T | 1 | a0002c0002t0001g0113 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.807-1518C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333444 | |||||||
| chr2:233333617 | C | G | 1 | a0001c0003t0001g0079 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.807-1345C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333617 | |||||||
| chr2:233333701 | C | T | 110 | a0001c0001t0001g0148 a0001c0001t0001g0154 a0001c0001t0001g0159 others(107): Show |
116 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.807-1261C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333701 | |||||||
| chr2:233333850 | G | T | 1 | a0001c0001t0001g0193 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.807-1112G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333850 | |||||||
| chr2:233333859 | C | G | 1 | a0001c0001t0001g0240 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.807-1103C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333859 | |||||||
| chr2:233334097 | AG | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0203 a0001c0001t0001g0273 others(2): Show |
6 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.807-864delG | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334097 | |||||||
| chr2:233334203 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.807-759C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334203 | |||||||
| chr2:233334204 | A | T | 1 | a0002c0005t0001g0005 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.807-758A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334204 | |||||||
| chr2:233334238 | C | T | 2 | a0002c0007t0001g0072 a0002c0007t0001g0073 |
2 | HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.807-724C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334238 | |||||||
| chr2:233334313 | G | C | 1 | a0002c0002t0001g0176 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.807-649G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334313 | |||||||
| chr2:233334504 | G | A | 79 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(76): Show |
83 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.807-458G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334504 | |||||||
| chr2:233334594 | C | T | 1 | a0002c0002t0001g0217 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.807-368C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334594 | |||||||
| chr2:233334630 | C | T | 6 | a0001c0006t0001g0118 a0001c0006t0001g0286 a0001c0006t0001g0292 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.807-332C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334630 | |||||||
| chr2:233334676 | T | C | 212 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(209): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.807-286T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334676 | |||||||
| chr2:233334769 | T | A | 1 | a0002c0002t0001g0112 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.807-193T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334769 | |||||||
| chr2:233334792 | C | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(16): Show |
21 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.807-170C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334792 | |||||||
| chr2:233334806 | C | A | 1 | a0003c0004t0001g0138 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.807-156C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334806 | |||||||
| chr2:233334811 | C | T | 8 | a0002c0005t0001g0281 a0002c0005t0001g0282 a0002c0005t0001g0283 others(5): Show |
8 | HG02965.hp1 HG03453.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.807-151C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334811 | |||||||
| chr2:233334812 | G | A | 10 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0058 others(7): Show |
10 | HG02074.hp2 HG02083.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.807-150G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334812 | |||||||
| chr2:233334936 | A | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0002c0009t0001g0280 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.807-26A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334936 | |||||||
| chr2:233334937 | A | G | 16 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0104 others(13): Show |
18 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.807-25A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334937 | |||||||
| chr2:233335191 | C | T | 7 | a0002c0005t0001g0281 a0002c0005t0001g0282 a0002c0005t0001g0283 others(4): Show |
7 | HG02965.hp1 HG03453.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.944+92C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335191 | |||||||
| chr2:233335231 | T | C | 1 | a0002c0010t0001g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.944+132T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335231 | |||||||
| chr2:233335242 | G | C | 1 | a0002c0002t0001g0058 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.944+143G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335242 | |||||||
| chr2:233335422 | T | C | 1 | a0002c0002t0001g0160 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.944+323T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335422 | |||||||
| chr2:233335464 | G | A | 2 | a0002c0002t0001g0173 a0002c0002t0001g0174 |
2 | HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.944+365G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335464 | |||||||
| chr2:233335558 | G | A | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0006t0001g0118 others(15): Show |
18 | HG02145.hp1 HG02258.hp1 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.944+459G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335558 | |||||||
| chr2:233335575 | G | GTTCA | 113 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(110): Show |
122 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.944+496_944+499dup others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 233335575 | ||||||
| chr2:233335575 | G | GTTCATTC others(1): Show |
6 | a0002c0005t0001g0281 a0002c0005t0001g0282 a0002c0005t0001g0283 others(3): Show |
6 | HG02965.hp1 HG03453.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.944+492_944+499dup others(8): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 233335575 | ||||||
| chr2:233335672 | C | T | 175 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(172): Show |
185 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.944+573C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335672 | |||||||
| chr2:233335749 | G | A | 30 | a0002c0005t0001g0039 a0002c0005t0001g0194 a0002c0005t0001g0199 others(27): Show |
31 | HG01433.hp2 HG01934.hp2 HG01981.hp1 others(28): Show |
intron_variant | MODIFIER | c.944+650G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335749 | |||||||
| chr2:233335759 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0305 a0001c0001t0001g0307 others(3): Show |
7 | HG02109.hp2 HG02622.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.944+660C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335759 | |||||||
| chr2:233336059 | T | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0104 others(8): Show |
13 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.944+960T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336059 | |||||||
| chr2:233336103 | A | C | 1 | a0003c0004t0001g0129 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.944+1004A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336103 | |||||||
| chr2:233336228 | G | A | 7 | a0002c0005t0001g0281 a0002c0005t0001g0282 a0002c0005t0001g0283 others(4): Show |
7 | HG02965.hp1 HG03453.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.944+1129G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336228 | |||||||
| chr2:233336399 | C | T | 1 | a0002c0002t0001g0162 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.944+1300C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336399 | |||||||
| chr2:233336499 | G | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(14): Show |
19 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.944+1400G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336499 | |||||||
| chr2:233336515 | G | GA | 24 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0103 others(21): Show |
24 | HG00140.hp1 HG00280.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.944+1429dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 233336515 | ||||||
| chr2:233336587 | AT | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.944+1491delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 233336587 | ||||||
| chr2:233336738 | G | A | 31 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(28): Show |
31 | HG00323.hp1 HG00423.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.944+1639G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336738 | |||||||
| chr2:233336754 | C | T | 11 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0058 others(8): Show |
11 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.944+1655C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336754 | |||||||
| chr2:233336786 | C | T | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | NA18952.hp2 NA18956.hp1 NA19001.hp1 others(4): Show |
intron_variant | MODIFIER | c.944+1687C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336786 | |||||||
| chr2:233336993 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.945-1683G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336993 | |||||||
| chr2:233337095 | C | CA | 13 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0104 others(10): Show |
15 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.945-1567dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 233337095 | ||||||
| chr2:233337095 | CA | C | 118 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0077 others(115): Show |
125 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.945-1567delA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 233337095 | ||||||
| chr2:233337234 | A | G | 1 | a0002c0002t0001g0335 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.945-1442A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337234 | |||||||
| chr2:233337247 | AT | A | 209 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(206): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.945-1420delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 233337247 | ||||||
| chr2:233337250 | T | G | 45 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0001c0001t0007g0069 others(42): Show |
47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.945-1426T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337250 | |||||||
| chr2:233337392 | C | G | 32 | a0002c0005t0001g0039 a0002c0005t0001g0194 a0002c0005t0001g0199 others(29): Show |
33 | HG01433.hp2 HG01934.hp2 HG01981.hp1 others(30): Show |
intron_variant | MODIFIER | c.945-1284C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337392 | |||||||
| chr2:233337395 | C | T | 1 | a0003c0016t0001g0133 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.945-1281C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337395 | |||||||
| chr2:233337485 | C | T | 1 | a0001c0003t0001g0091 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.945-1191C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337485 | |||||||
| chr2:233337491 | C | G | 180 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(177): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.945-1185C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337491 | |||||||
| chr2:233337579 | T | C | 190 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(187): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.945-1097T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337579 | |||||||
| chr2:233337618 | C | T | 96 | a0001c0001t0001g0164 a0001c0001t0001g0175 a0001c0001t0001g0297 others(93): Show |
103 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.945-1058C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337618 | |||||||
| chr2:233337724 | T | C | 139 | a0001c0001t0001g0164 a0001c0001t0001g0175 a0001c0001t0001g0297 others(136): Show |
147 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.945-952T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337724 | |||||||
| chr2:233337812 | T | C | 96 | a0001c0001t0001g0164 a0001c0001t0001g0175 a0001c0001t0001g0297 others(93): Show |
103 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.945-864T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337812 | |||||||
| chr2:233337857 | C | T | 32 | a0002c0005t0001g0039 a0002c0005t0001g0194 a0002c0005t0001g0199 others(29): Show |
33 | HG01433.hp2 HG01934.hp2 HG01981.hp1 others(30): Show |
intron_variant | MODIFIER | c.945-819C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337857 | |||||||
| chr2:233337892 | A | G | 2 | a0001c0003t0001g0290 a0001c0003t0001g0291 |
2 | HG00323.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.945-784A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337892 | |||||||
| chr2:233337899 | G | C | 1 | a0001c0003t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.945-777G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337899 | |||||||
| chr2:233337902 | C | T | 1 | a0001c0003t0001g0100 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.945-774C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337902 | |||||||
| chr2:233337976 | C | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.945-700C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337976 | |||||||
| chr2:233338152 | G | A | 26 | a0001c0001t0001g0054 a0001c0001t0001g0109 a0001c0001t0001g0119 others(23): Show |
26 | HG00438.hp2 HG00609.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.945-524G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338152 | |||||||
| chr2:233338164 | G | A | 1 | a0001c0003t0001g0079 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.945-512G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338164 | |||||||
| chr2:233338299 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.945-377C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338299 | |||||||
| chr2:233338348 | A | G | 95 | a0001c0001t0001g0164 a0001c0001t0001g0175 a0001c0001t0001g0297 others(92): Show |
101 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.945-328A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338348 | |||||||
| chr2:233338491 | G | A | 3 | a0002c0002t0001g0123 a0002c0002t0001g0181 a0002c0002t0001g0182 |
3 | HG00733.hp1 HG00741.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.945-185G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338491 | |||||||
| chr2:233338517 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.945-159C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338517 | |||||||
| chr2:233338618 | T | C | 1 | a0002c0002t0001g0156 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.945-58T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338618 | |||||||
| chr2:233338619 | C | T | 1 | a0002c0002t0001g0156 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.945-57C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338619 | |||||||
| chr2:233338620 | T | A | 1 | a0002c0002t0001g0156 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.945-56T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338620 | |||||||
| chr2:233338862 | C | G | 34 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0001c0001t0007g0069 others(31): Show |
36 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.1022+109C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233338862 | |||||||
| chr2:233338981 | T | C | 210 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(207): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1022+228T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233338981 | |||||||
| chr2:233339278 | G | A | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(176): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1022+525G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339278 | |||||||
| chr2:233339464 | C | G | 179 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0064 others(176): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1022+711C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339464 | |||||||
| chr2:233339537 | G | GT | 32 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(29): Show |
33 | HG00621.hp2 HG00738.hp1 HG01978.hp2 others(30): Show |
intron_variant | MODIFIER | c.1022+803dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 233339537 | ||||||
| chr2:233339537 | G | GTT | 16 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0104 others(13): Show |
18 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1022+802_1022+803d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 233339537 | ||||||
| chr2:233339537 | GT | G | 89 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0067 others(86): Show |
95 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1022+803delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 233339537 | ||||||
| chr2:233339542 | T | G | 1 | a0001c0001t0006g0296 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1022+789T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339542 | |||||||
| chr2:233339556 | T | C | 94 | a0001c0001t0001g0164 a0001c0001t0001g0175 a0001c0001t0001g0297 others(91): Show |
100 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1022+803T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339556 | |||||||
| chr2:233339557 | C | G | 11 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0058 others(8): Show |
11 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1022+804C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339557 | |||||||
| chr2:233339563 | G | A | 1 | a0001c0003t0001g0079 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1022+810G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339563 | |||||||
| chr2:233339700 | ATC | A | 208 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(205): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1023-750_1023-749d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 233339700 | ||||||
| chr2:233339702 | C | CTCACTCT others(8805): Show |
1 | a0004c0008t0001g0075 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1023-751_1023-750i others(8814): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 233339702 | ||||||
| chr2:233339851 | C | T | 3 | a0002c0010t0001g0068 a0002c0010t0001g0085 a0002c0010t0001g0102 |
3 | HG02257.hp1 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1023-604C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339851 | |||||||
| chr2:233339880 | C | G | 1 | a0002c0007t0001g0072 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1023-575C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339880 | |||||||
| chr2:233339882 | C | T | 1 | a0002c0005t0001g0005 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1023-573C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339882 | |||||||
| chr2:233339883 | G | A | 94 | a0001c0001t0001g0164 a0001c0001t0001g0175 a0001c0001t0001g0297 others(91): Show |
100 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1023-572G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339883 | |||||||
| chr2:233339901 | G | A | 37 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(34): Show |
38 | HG01109.hp2 HG01433.hp2 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.1023-554G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339901 | |||||||
| chr2:233339964 | C | CT | 128 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(125): Show |
135 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1023-481dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 233339964 | ||||||
| chr2:233339973 | T | C | 18 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0027 others(15): Show |
18 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1023-482T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339973 | |||||||
| chr2:233339999 | C | T | 45 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0001c0001t0007g0069 others(42): Show |
47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1023-456C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339999 | |||||||
| chr2:233340097 | C | A | 1 | a0001c0001t0001g0221 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1023-358C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233340097 | |||||||
| chr2:233340107 | C | T | 37 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(34): Show |
38 | HG01109.hp2 HG01433.hp2 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.1023-348C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233340107 | |||||||
| chr2:233340209 | G | A | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0006t0001g0118 others(13): Show |
16 | HG02145.hp1 HG02647.hp2 HG02922.hp2 others(13): Show |
intron_variant | MODIFIER | c.1023-246G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233340209 | |||||||
| chr2:233340362 | T | C | 1 | a0002c0009t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1023-93T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233340362 | |||||||
| chr2:233340436 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1023-19G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233340436 | |||||||
| chr2:233340551 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1046+73G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233340551 | |||||||
| chr2:233340618 | G | A | 11 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0058 others(8): Show |
11 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1046+140G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233340618 | |||||||
| chr2:233340739 | C | T | 94 | a0001c0001t0001g0164 a0001c0001t0001g0175 a0001c0001t0001g0297 others(91): Show |
100 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1046+261C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233340739 | |||||||
| chr2:233340751 | T | TTG | 59 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0103 others(56): Show |
63 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1046+291_1046+292d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 233340751 | ||||||
| chr2:233340751 | TTG | T | 130 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(127): Show |
137 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1046+291_1046+292d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 233340751 | ||||||
| chr2:233340809 | T | C | 1 | a0002c0007t0001g0080 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1046+331T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233340809 | |||||||
| chr2:233340925 | C | T | 11 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0058 others(8): Show |
11 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1046+447C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233340925 | |||||||
| chr2:233341034 | G | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0104 others(9): Show |
14 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1046+556G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341034 | |||||||
| chr2:233341089 | T | C | 131 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(128): Show |
138 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1046+611T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341089 | |||||||
| chr2:233341132 | G | A | 7 | a0002c0005t0001g0281 a0002c0005t0001g0282 a0002c0005t0001g0283 others(4): Show |
7 | HG02965.hp1 HG03453.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1046+654G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341132 | |||||||
| chr2:233341265 | T | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0103 others(10): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1046+787T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341265 | |||||||
| chr2:233341275 | C | A | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0103 others(57): Show |
64 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.1046+797C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341275 | |||||||
| chr2:233341378 | G | A | 5 | a0001c0003t0001g0094 a0001c0003t0001g0096 a0001c0003t0001g0097 others(2): Show |
5 | HG02257.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1047-893G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341378 | |||||||
| chr2:233341836 | A | G | 94 | a0001c0001t0001g0164 a0001c0001t0001g0175 a0001c0001t0001g0297 others(91): Show |
100 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1047-435A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341836 | |||||||
| chr2:233341866 | C | A | 1 | a0002c0002t0001g0056 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1047-405C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341866 | |||||||
| chr2:233342123 | C | CA | 141 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(138): Show |
151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1047-131dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 233342123 | ||||||
| chr2:233342123 | C | CAA | 10 | a0001c0003t0001g0081 a0001c0003t0001g0082 a0001c0003t0003g0088 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1047-132_1047-131d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 233342123 | ||||||
| chr2:233342258 | T | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0104 others(10): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1047-13T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233342258 | |||||||
| chr2:233342410 | G | A | 1 | a0002c0002t0001g0042 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1102+84G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342410 | |||||||
| chr2:233342481 | A | G | 1 | a0001c0001t0006g0296 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1102+155A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342481 | |||||||
| chr2:233342550 | TA | T | 5 | a0001c0003t0001g0094 a0001c0003t0001g0096 a0001c0003t0001g0097 others(2): Show |
5 | HG02257.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1102+225delA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342550 | |||||||
| chr2:233342676 | T | G | 139 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(136): Show |
148 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.1102+350T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342676 | |||||||
| chr2:233342715 | G | C | 1 | a0002c0005t0001g0005 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1102+389G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342715 | |||||||
| chr2:233342762 | A | AT | 30 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0054 others(27): Show |
30 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1102+451dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233342762 | ||||||
| chr2:233342790 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1102+464C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342790 | |||||||
| chr2:233342804 | G | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1102+478G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342804 | |||||||
| chr2:233342827 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1102+501A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342827 | |||||||
| chr2:233343063 | T | C | 1 | a0001c0001t0001g0271 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1102+737T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343063 | |||||||
| chr2:233343069 | T | G | 9 | a0002c0010t0001g0289 a0003c0004t0001g0129 a0003c0004t0001g0132 others(6): Show |
9 | NA18944.hp1 NA18966.hp1 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.1102+743T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343069 | |||||||
| chr2:233343077 | T | G | 1 | a0001c0003t0001g0099 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1102+751T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343077 | |||||||
| chr2:233343077 | T | TG | 11 | a0001c0001t0001g0159 a0002c0002t0001g0007 a0002c0002t0001g0040 others(8): Show |
11 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1102+755dupG | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233343077 | ||||||
| chr2:233343081 | G | GT | 127 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(124): Show |
133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1102+777dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233343081 | ||||||
| chr2:233343081 | G | GTT | 27 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0030 others(24): Show |
27 | HG00423.hp2 HG00735.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1102+776_1102+777d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233343081 | ||||||
| chr2:233343081 | G | GTTT | 7 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0059 others(4): Show |
7 | HG02083.hp1 HG02132.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.1102+775_1102+777d others(5): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233343081 | ||||||
| chr2:233343081 | G | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0051 |
2 | HG02647.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1102+755G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343081 | |||||||
| chr2:233343081 | GT | G | 11 | a0001c0003t0001g0004 a0001c0003t0001g0079 a0001c0003t0001g0081 others(8): Show |
12 | HG02080.hp1 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1102+777delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233343081 | ||||||
| chr2:233343081 | GTTTTT | G | 39 | a0001c0001t0001g0077 a0002c0005t0001g0009 a0002c0005t0001g0039 others(36): Show |
41 | HG00741.hp2 HG01261.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.1102+773_1102+777d others(7): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233343081 | ||||||
| chr2:233343082 | T | G | 70 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0010 others(67): Show |
76 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1102+756T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343082 | |||||||
| chr2:233343083 | T | G | 5 | a0002c0002t0001g0042 a0002c0002t0001g0112 a0002c0002t0001g0206 others(2): Show |
5 | HG02080.hp1 NA18945.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102+757T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343083 | |||||||
| chr2:233343236 | C | A | 1 | a0002c0002t0001g0160 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1102+910C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343236 | |||||||
| chr2:233343261 | G | T | 207 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(204): Show |
220 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.1102+935G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343261 | |||||||
| chr2:233343372 | G | A | 2 | a0002c0010t0001g0068 a0002c0010t0001g0085 |
2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1102+1046G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343372 | |||||||
| chr2:233343378 | C | T | 4 | a0001c0006t0001g0118 a0001c0006t0001g0292 a0002c0009t0001g0078 others(1): Show |
4 | HG02145.hp1 HG02976.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1102+1052C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343378 | |||||||
| chr2:233343903 | T | C | 2 | a0002c0005t0001g0283 a0011c0013t0001g0285 |
2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1102+1577T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343903 | |||||||
| chr2:233343912 | C | T | 1 | a0001c0003t0001g0317 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1102+1586C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343912 | |||||||
| chr2:233343971 | A | G | 4 | a0002c0002t0001g0042 a0002c0007t0001g0072 a0002c0007t0001g0073 others(1): Show |
4 | HG02080.hp1 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1102+1645A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343971 | |||||||
| chr2:233344228 | T | A | 1 | a0002c0005t0001g0039 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1102+1902T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344228 | |||||||
| chr2:233344240 | G | A | 1 | a0002c0005t0001g0005 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1102+1914G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344240 | |||||||
| chr2:233344257 | G | A | 81 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0001g0066 others(78): Show |
85 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.1102+1931G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344257 | |||||||
| chr2:233344264 | G | A | 91 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(88): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1102+1938G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344264 | |||||||
| chr2:233344318 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1102+1992G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344318 | |||||||
| chr2:233344339 | T | G | 32 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(29): Show |
34 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1102+2013T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344339 | |||||||
| chr2:233344438 | T | C | 1 | a0001c0001t0006g0296 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1103-1965T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344438 | |||||||
| chr2:233344450 | C | T | 2 | a0001c0003t0003g0087 a0001c0003t0003g0088 |
2 | NA18940.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1103-1953C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344450 | |||||||
| chr2:233344467 | G | A | 1 | a0002c0005t0001g0005 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1103-1936G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344467 | |||||||
| chr2:233344503 | C | A | 1 | a0001c0001t0001g0225 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1103-1900C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344503 | |||||||
| chr2:233344505 | A | G | 1 | a0002c0002t0001g0058 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1103-1898A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344505 | |||||||
| chr2:233344666 | A | C | 1 | a0002c0002t0001g0332 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1103-1737A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344666 | |||||||
| chr2:233344723 | G | A | 1 | a0001c0001t0006g0296 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1103-1680G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344723 | |||||||
| chr2:233344951 | A | C | 110 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(107): Show |
119 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1103-1452A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344951 | |||||||
| chr2:233345001 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1103-1402T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233345001 | |||||||
| chr2:233345041 | C | T | 1 | a0001c0003t0001g0291 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1103-1362C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233345041 | |||||||
| chr2:233345316 | G | C | 53 | a0001c0001t0001g0017 a0001c0001t0001g0077 a0001c0006t0001g0118 others(50): Show |
55 | HG00741.hp2 HG01261.hp1 HG01433.hp2 others(52): Show |
intron_variant | MODIFIER | c.1103-1087G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233345316 | |||||||
| chr2:233345419 | A | G | 49 | a0001c0001t0001g0017 a0001c0001t0001g0077 a0002c0005t0001g0009 others(46): Show |
51 | HG00741.hp2 HG01261.hp1 HG01433.hp2 others(48): Show |
intron_variant | MODIFIER | c.1103-984A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233345419 | |||||||
| chr2:233345585 | G | A | 32 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(29): Show |
34 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1103-818G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233345585 | |||||||
| chr2:233345628 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1103-775G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233345628 | |||||||
| chr2:233346000 | A | G | 5 | a0002c0005t0001g0281 a0002c0005t0001g0282 a0002c0005t0001g0287 others(2): Show |
5 | HG03453.hp1 HG03486.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1103-403A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233346000 | |||||||
| chr2:233346054 | G | T | 3 | a0001c0006t0001g0121 a0001c0006t0001g0122 a0001c0006t0001g0279 |
3 | HG03130.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1103-349G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233346054 | |||||||
| chr2:233346061 | G | A | 32 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(29): Show |
34 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1103-342G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233346061 | |||||||
| chr2:233346130 | G | C | 1 | a0001c0001t0001g0263 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1103-273G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233346130 | |||||||
| chr2:233346164 | T | TAATAAAA others(3): Show |
101 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(98): Show |
107 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1103-234_1103-225d others(12): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233346164 | ||||||
| chr2:233346179 | T | A | 1 | a0001c0001t0001g0297 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1103-224T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233346179 | |||||||
| chr2:233346244 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1103-159C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233346244 | |||||||
| chr2:233346276 | T | A | 1 | a0001c0001t0001g0297 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1103-127T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233346276 | |||||||
| chr2:233346499 | A | C | 49 | a0002c0002t0001g0002 a0002c0002t0001g0016 a0002c0002t0001g0040 others(46): Show |
53 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1112+87A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 15/15 | chr2 | 233346499 | |||||||
| chr2:233346499 | A | G | 1 | a0002c0002t0001g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1112+87A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 15/15 | chr2 | 233346499 | |||||||
| chr2:233346578 | G | A | 2 | a0001c0006t0001g0118 a0001c0006t0001g0292 |
2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1112+166G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 15/15 | chr2 | 233346578 | |||||||
| chr2:233346587 | C | T | 1 | a0001c0003t0001g0337 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1112+175C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 15/15 | chr2 | 233346587 | |||||||
| chr2:233346625 | T | A | 1 | a0001c0001t0001g0027 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1113-182T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 15/15 | chr2 | 233346625 | |||||||
| chr2:233346698 | A | G | 1 | a0002c0007t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1113-109A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 15/15 | chr2 | 233346698 | |||||||
| chr2:233346732 | A | T | 1 | a0001c0001t0001g0027 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1113-75A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 15/15 | chr2 | 233346732 |