Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1278 |
| ensemblid | ENSG00000164692.19 |
| hgncid | 2198 |
| symbol | COL1A2 |
| name | collagen type I alpha 2 chain |
| refseq_nuc | NM_000089.4 |
| refseq_prot | NP_000080.2 |
| ensembl_nuc | ENST00000297268.11 |
| ensembl_prot | ENSP00000297268.6 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 94394895 |
| end | 94431227 |
| strand | + |
| ver | v1.2 |
| region | chr7:94394895-94431227 |
| region5000 | chr7:94389895-94436227 |
| regionname0 | COL1A2_chr7_94394895_94431227 |
| regionname5000 | COL1A2_chr7_94389895_94436227 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1366 | 364 | 82 | 62 | 183 | 5 | 31 | 144 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(1361): Show |
chr7 | 94389895 | 94436227 |
| a0002 | 1/0 | 1366 | 58 | 8 | 9 | 15 | 8 | 17 | 8 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(1361): Show |
chr7 | 94389895 | 94436227 |
| a0003 | 0/0 | 1366 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(1361): Show |
chr7 | 94389895 | 94436227 |
| a0004 | 0/0 | 1366 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(1361): Show |
chr7 | 94389895 | 94436227 |
| a0005 | 0/0 | 1366 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(1361): Show |
chr7 | 94389895 | 94436227 |
| a0006 | 0/0 | 1366 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(1361): Show |
chr7 | 94389895 | 94436227 |
| a0007 | 0/0 | 1366 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(1361): Show |
chr7 | 94389895 | 94436227 |
| a0008 | 0/0 | 1366 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(1361): Show |
chr7 | 94389895 | 94436227 |
| a0009 | 0/0 | 829 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(824): Show |
chr7 | 94389895 | 94436227 |
| a0010 | 0/0 | 1366 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(1361): Show |
chr7 | 94389895 | 94436227 |
| a0011 | 0/0 | 1366 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(1361): Show |
chr7 | 94389895 | 94436227 |
| a0012 | 0/0 | 1366 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(1361): Show |
chr7 | 94389895 | 94436227 |
| a0013 | 0/0 | 1366 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(1361): Show |
chr7 | 94389895 | 94436227 |
| a0014 | 0/0 | 1281 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(1276): Show |
chr7 | 94389895 | 94436227 |
| a0015 | 0/0 | 1366 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | MLSFV others(1361): Show |
chr7 | 94389895 | 94436227 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4098 | 91 | 28 | 29 | 22 | 1 | 10 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0002 | 0/0 | 4098 | 78 | 5 | 18 | 48 | 1 | 6 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0003 | 0/0 | 4098 | 70 | 0 | 1 | 68 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0005 | 0/0 | 4098 | 38 | 0 | 3 | 22 | 0 | 13 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0006 | 0/0 | 4098 | 34 | 5 | 10 | 16 | 3 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0007 | 0/0 | 4098 | 16 | 14 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0008 | 0/0 | 4098 | 15 | 15 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0009 | 0/0 | 4098 | 8 | 7 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0011 | 0/0 | 4098 | 3 | 0 | 0 | 3 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0014 | 0/0 | 4098 | 2 | 1 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0015 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0017 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0020 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0021 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0022 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0024 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0029 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0035 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0001c0037 | 0/0 | 4098 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0002c0004 | 1/0 | 4098 | 53 | 6 | 9 | 12 | 8 | 17 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0002c0010 | 0/0 | 4098 | 3 | 0 | 0 | 3 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0002c0019 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0002c0026 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0003c0013 | 0/0 | 4098 | 2 | 1 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0003c0033 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0004c0012 | 0/0 | 4098 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0005c0030 | 0/0 | 4098 | 1 | 0 | 0 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0006c0016 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0007c0031 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0008c0018 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0009c0034 | 0/0 | 4098 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0010c0027 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0011c0025 | 0/0 | 4098 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0012c0036 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0013c0032 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 | ||
| a0014c0028 | 0/0 | 4085 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4080): Show |
chr7 | 94389895 | 94436227 | ||
| a0015c0023 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | ATGCT others(4093): Show |
chr7 | 94389895 | 94436227 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5079 | 45 | 22 | 10 | 11 | 1 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0001t0002 | 0/0 | 5079 | 33 | 1 | 15 | 10 | 0 | 7 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0001t0003 | 0/1 | 5072 | 8 | 1 | 4 | 0 | 0 | 2 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5067): Show |
chr7 | 94389895 | 94436227 |
| a0001c0001t0004 | 0/0 | 5079 | 2 | 1 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0001t0005 | 0/0 | 5079 | 3 | 3 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0002t0001 | 0/0 | 5079 | 58 | 3 | 7 | 44 | 0 | 4 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0002t0002 | 0/0 | 5079 | 6 | 0 | 1 | 4 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0002t0003 | 0/0 | 5072 | 12 | 1 | 9 | 0 | 1 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5067): Show |
chr7 | 94389895 | 94436227 |
| a0001c0002t0004 | 0/0 | 5079 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0002t0006 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0003t0001 | 0/0 | 5079 | 50 | 0 | 1 | 48 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0003t0002 | 0/0 | 5079 | 12 | 0 | 0 | 12 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0003t0003 | 0/0 | 5072 | 7 | 0 | 0 | 7 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5067): Show |
chr7 | 94389895 | 94436227 |
| a0001c0003t0004 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0005t0001 | 0/0 | 5079 | 22 | 0 | 2 | 14 | 0 | 6 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0005t0002 | 0/0 | 5079 | 10 | 0 | 1 | 3 | 0 | 6 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0005t0003 | 0/0 | 5072 | 6 | 0 | 0 | 5 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5067): Show |
chr7 | 94389895 | 94436227 |
| a0001c0006t0001 | 0/0 | 5079 | 10 | 3 | 2 | 4 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0006t0002 | 0/0 | 5079 | 5 | 1 | 3 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0006t0003 | 0/0 | 5072 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5067): Show |
chr7 | 94389895 | 94436227 |
| a0001c0006t0004 | 0/0 | 5079 | 18 | 1 | 4 | 12 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0007t0001 | 0/0 | 5079 | 10 | 8 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0007t0004 | 0/0 | 5079 | 4 | 4 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0007t0005 | 0/0 | 5079 | 2 | 2 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0008t0001 | 0/0 | 5079 | 14 | 14 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0008t0003 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5067): Show |
chr7 | 94389895 | 94436227 |
| a0001c0009t0001 | 0/0 | 5079 | 4 | 3 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0009t0003 | 0/0 | 5072 | 4 | 4 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5067): Show |
chr7 | 94389895 | 94436227 |
| a0001c0011t0001 | 0/0 | 5079 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0011t0003 | 0/0 | 5072 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5067): Show |
chr7 | 94389895 | 94436227 |
| a0001c0014t0001 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0014t0002 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0015t0005 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0017t0006 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0020t0003 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5067): Show |
chr7 | 94389895 | 94436227 |
| a0001c0021t0001 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0022t0001 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0024t0001 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0029t0007 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0035t0001 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0001c0037t0002 | 0/0 | 5079 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0002c0004t0001 | 0/0 | 5079 | 8 | 2 | 0 | 2 | 0 | 4 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0002c0004t0002 | 0/0 | 5079 | 24 | 2 | 2 | 6 | 4 | 10 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0002c0004t0003 | 1/0 | 5072 | 20 | 1 | 7 | 4 | 4 | 3 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5067): Show |
chr7 | 94389895 | 94436227 |
| a0002c0004t0004 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0002c0010t0003 | 0/0 | 5072 | 3 | 0 | 0 | 3 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5067): Show |
chr7 | 94389895 | 94436227 |
| a0002c0019t0001 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0002c0026t0001 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0003c0013t0001 | 0/0 | 5079 | 2 | 1 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0003c0033t0001 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0004c0012t0001 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0004c0012t0004 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0005c0030t0001 | 0/0 | 5079 | 1 | 0 | 0 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0006c0016t0001 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0007c0031t0001 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0008c0018t0001 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0009c0034t0001 | 0/0 | 5079 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0010c0027t0001 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0011c0025t0001 | 0/0 | 5079 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0012c0036t0001 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0013c0032t0001 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| a0014c0028t0002 | 0/0 | 5066 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5061): Show |
chr7 | 94389895 | 94436227 |
| a0015c0023t0004 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | AGCAC others(5074): Show |
chr7 | 94389895 | 94436227 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0022 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0023 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0062 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0002 | 0/0 | 17 | 0 | 10 | 3 | 0 | 4 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0003g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0001 | 0/0 | 27 | 0 | 3 | 22 | 0 | 2 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0003g0011 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0003g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0003g0031 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0002t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0003 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0002g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0002g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0003g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0003g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0003t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0001g0010 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0002g0026 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0002g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0005t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0002g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0004g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0004g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0004g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0006t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0007t0001g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0007t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0007t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0007t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0007t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0007t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0007t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0007t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0007t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0007t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0007t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0007t0005g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0008t0001g0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0008t0001g0061 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0008t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0008t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0008t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0008t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0008t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0009t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0009t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0009t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0009t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0009t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0009t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0009t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0009t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0011t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0011t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0011t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0014t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0014t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0015t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0017t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0020t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0021t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0022t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0024t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0029t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0035t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0001c0037t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0012 | 0/0 | 5 | 1 | 1 | 0 | 0 | 3 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0003g0020 | 1/0 | 4 | 1 | 1 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0003g0027 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0003g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0004t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0010t0003g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0019t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0002c0026t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0003c0013t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0003c0013t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0003c0033t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0004c0012t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0004c0012t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0005c0030t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0006c0016t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0007c0031t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0008c0018t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0009c0034t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0010c0027t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0011c0025t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0012c0036t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0013c0032t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0014c0028t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| a0015c0023t0004g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0006 | t0001 | g0024 | EUR | GBR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00280 | hp1 | a0002 | c0004 | t0002 | g0028 | EUR | FIN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00280 | hp2 | a0001 | c0006 | t0002 | g0035 | EUR | FIN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00323 | hp1 | a0005 | c0030 | t0001 | g0096 | EUR | FIN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00323 | hp2 | a0002 | c0004 | t0003 | g0028 | EUR | FIN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0228 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00438 | hp2 | a0001 | c0006 | t0004 | g0004 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00544 | hp1 | a0002 | c0004 | t0002 | g0186 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00558 | hp1 | a0001 | c0005 | t0002 | g0123 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00558 | hp2 | a0001 | c0003 | t0002 | g0223 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00597 | hp2 | a0001 | c0003 | t0001 | g0225 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00609 | hp2 | a0002 | c0004 | t0003 | g0153 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00621 | hp1 | a0001 | c0005 | t0001 | g0125 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00621 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0011 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00642 | hp2 | a0002 | c0004 | t0002 | g0141 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | CHS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00733 | hp1 | a0001 | c0006 | t0002 | g0035 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00735 | hp1 | a0001 | c0006 | t0004 | g0016 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00738 | hp1 | a0001 | c0009 | t0001 | g0139 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01069 | hp1 | a0001 | c0006 | t0004 | g0032 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01070 | hp1 | a0001 | c0006 | t0004 | g0032 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01081 | hp1 | a0002 | c0004 | t0003 | g0143 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01081 | hp2 | a0002 | c0004 | t0002 | g0012 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01099 | hp1 | a0001 | c0006 | t0002 | g0080 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01106 | hp1 | a0001 | c0006 | t0001 | g0024 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0017 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01109 | hp2 | a0002 | c0004 | t0003 | g0132 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01167 | hp2 | a0001 | c0006 | t0002 | g0081 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01175 | hp1 | a0001 | c0005 | t0001 | g0010 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01175 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01192 | hp2 | a0002 | c0004 | t0003 | g0020 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0017 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01243 | hp2 | a0003 | c0013 | t0001 | g0066 | AMR | PUR | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01255 | hp1 | a0002 | c0004 | t0003 | g0028 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01256 | hp1 | a0001 | c0006 | t0004 | g0016 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0031 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01258 | hp1 | a0001 | c0002 | t0003 | g0031 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01261 | hp1 | a0001 | c0002 | t0004 | g0124 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01346 | hp1 | a0001 | c0006 | t0003 | g0016 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01433 | hp1 | a0001 | c0005 | t0001 | g0010 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0093 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01496 | hp2 | a0002 | c0004 | t0003 | g0027 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01515 | hp1 | a0002 | c0004 | t0003 | g0156 | EUR | IBS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0031 | EUR | IBS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01517 | hp1 | a0001 | c0006 | t0004 | g0016 | EUR | IBS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01517 | hp2 | a0002 | c0004 | t0003 | g0027 | EUR | IBS | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01891 | hp2 | a0001 | c0002 | t0006 | g0084 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0226 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01943 | hp2 | a0002 | c0004 | t0003 | g0149 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01952 | hp1 | a0002 | c0004 | t0003 | g0148 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01981 | hp1 | a0001 | c0005 | t0002 | g0043 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02015 | hp1 | a0002 | c0004 | t0001 | g0145 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02027 | hp1 | a0002 | c0004 | t0003 | g0020 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02027 | hp2 | a0001 | c0005 | t0003 | g0007 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02040 | hp2 | a0006 | c0016 | t0001 | g0236 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02055 | hp1 | a0001 | c0007 | t0001 | g0021 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02055 | hp2 | a0001 | c0009 | t0003 | g0245 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02056 | hp1 | a0001 | c0011 | t0001 | g0202 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02056 | hp2 | a0001 | c0014 | t0001 | g0109 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02071 | hp2 | a0002 | c0004 | t0003 | g0131 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02074 | hp2 | a0001 | c0005 | t0003 | g0007 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02080 | hp2 | a0001 | c0003 | t0003 | g0199 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02083 | hp1 | a0002 | c0004 | t0001 | g0075 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02129 | hp1 | a0001 | c0011 | t0001 | g0213 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02129 | hp2 | a0001 | c0003 | t0001 | g0060 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02132 | hp1 | a0001 | c0003 | t0003 | g0013 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02135 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02145 | hp2 | a0001 | c0007 | t0005 | g0056 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02155 | hp1 | a0001 | c0003 | t0003 | g0013 | EAS | CDX | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02155 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | CDX | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02165 | hp1 | a0002 | c0004 | t0002 | g0130 | EAS | CDX | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | CDX | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02257 | hp1 | a0001 | c0008 | t0003 | g0005 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02257 | hp2 | a0001 | c0009 | t0003 | g0241 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02258 | hp1 | a0001 | c0008 | t0001 | g0005 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02280 | hp2 | a0002 | c0004 | t0003 | g0020 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02451 | hp1 | a0001 | c0007 | t0004 | g0192 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02523 | hp2 | a0007 | c0031 | t0001 | g0091 | EAS | KHV | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02572 | hp1 | a0001 | c0007 | t0001 | g0194 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02572 | hp2 | a0001 | c0006 | t0002 | g0134 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02602 | hp1 | a0002 | c0004 | t0002 | g0070 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02602 | hp2 | a0001 | c0005 | t0001 | g0129 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02615 | hp1 | a0001 | c0009 | t0001 | g0137 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02615 | hp2 | a0001 | c0007 | t0005 | g0056 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02630 | hp1 | a0001 | c0008 | t0001 | g0189 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02630 | hp2 | a0002 | c0004 | t0001 | g0170 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02647 | hp1 | a0001 | c0008 | t0001 | g0005 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02647 | hp2 | a0001 | c0002 | t0003 | g0104 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02683 | hp1 | a0002 | c0004 | t0002 | g0158 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02698 | hp1 | a0002 | c0004 | t0003 | g0239 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02717 | hp1 | a0001 | c0024 | t0001 | g0133 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02717 | hp2 | a0001 | c0008 | t0001 | g0005 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02723 | hp1 | a0001 | c0007 | t0004 | g0185 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02723 | hp2 | a0001 | c0008 | t0001 | g0005 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02735 | hp2 | a0002 | c0004 | t0003 | g0027 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02738 | hp2 | a0001 | c0005 | t0002 | g0026 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02818 | hp1 | a0003 | c0013 | t0001 | g0065 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02818 | hp2 | a0001 | c0008 | t0001 | g0197 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02886 | hp2 | a0002 | c0004 | t0004 | g0164 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02896 | hp1 | a0001 | c0008 | t0001 | g0005 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02897 | hp2 | a0001 | c0008 | t0001 | g0005 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02922 | hp2 | a0001 | c0007 | t0004 | g0175 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02965 | hp1 | a0001 | c0007 | t0001 | g0021 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02965 | hp2 | a0002 | c0019 | t0001 | g0246 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02970 | hp1 | a0002 | c0004 | t0001 | g0142 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02970 | hp2 | a0008 | c0018 | t0001 | g0029 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03017 | hp1 | a0009 | c0034 | t0001 | g0039 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03017 | hp2 | a0002 | c0004 | t0002 | g0152 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03041 | hp2 | a0001 | c0008 | t0001 | g0198 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03098 | hp1 | a0001 | c0006 | t0001 | g0232 | AFR | MSL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0082 | AFR | MSL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03130 | hp1 | a0001 | c0008 | t0001 | g0061 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03130 | hp2 | a0001 | c0008 | t0001 | g0231 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03139 | hp2 | a0001 | c0007 | t0001 | g0021 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03195 | hp1 | a0001 | c0022 | t0001 | g0161 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | MSL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0108 | AFR | MSL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03225 | hp1 | a0001 | c0029 | t0007 | g0168 | AFR | MSL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03225 | hp2 | a0001 | c0020 | t0003 | g0242 | AFR | MSL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03239 | hp2 | a0002 | c0004 | t0002 | g0165 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03453 | hp1 | a0010 | c0027 | t0001 | g0052 | AFR | MSL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03453 | hp2 | a0001 | c0007 | t0001 | g0196 | AFR | MSL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | MSL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03486 | hp2 | a0001 | c0015 | t0005 | g0155 | AFR | MSL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03490 | hp1 | a0002 | c0004 | t0003 | g0147 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03491 | hp1 | a0001 | c0005 | t0001 | g0041 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03491 | hp2 | a0002 | c0004 | t0001 | g0140 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03492 | hp2 | a0001 | c0005 | t0001 | g0041 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03516 | hp2 | a0001 | c0006 | t0001 | g0048 | AFR | ESN | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03540 | hp1 | a0001 | c0007 | t0001 | g0174 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03540 | hp2 | a0001 | c0014 | t0002 | g0210 | AFR | GWD | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03579 | hp1 | a0001 | c0008 | t0001 | g0061 | AFR | MSL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03654 | hp1 | a0002 | c0004 | t0002 | g0012 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0183 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0017 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | STU | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03688 | hp2 | a0002 | c0004 | t0002 | g0012 | SAS | STU | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03710 | hp1 | a0002 | c0004 | t0002 | g0050 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03831 | hp1 | a0002 | c0004 | t0002 | g0144 | SAS | BEB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03831 | hp2 | a0001 | c0005 | t0002 | g0047 | SAS | BEB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03834 | hp1 | a0011 | c0025 | t0001 | g0064 | SAS | BEB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03834 | hp2 | a0001 | c0005 | t0001 | g0116 | SAS | BEB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03927 | hp1 | a0001 | c0005 | t0001 | g0074 | SAS | BEB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0151 | SAS | BEB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03942 | hp1 | a0002 | c0004 | t0001 | g0064 | SAS | BEB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG03942 | hp2 | a0001 | c0037 | t0002 | g0043 | SAS | BEB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG04115 | hp1 | a0002 | c0004 | t0001 | g0049 | SAS | STU | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG04115 | hp2 | a0002 | c0004 | t0002 | g0050 | SAS | STU | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG04184 | hp1 | a0001 | c0005 | t0002 | g0026 | SAS | BEB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG04184 | hp2 | a0002 | c0004 | t0002 | g0012 | SAS | BEB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | STU | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG04204 | hp1 | a0001 | c0005 | t0001 | g0107 | SAS | STU | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG04204 | hp2 | a0001 | c0005 | t0002 | g0047 | SAS | STU | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG04228 | hp1 | a0002 | c0004 | t0001 | g0049 | SAS | STU | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG04228 | hp2 | a0001 | c0005 | t0002 | g0026 | SAS | STU | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | YRI | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | CHB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18747 | hp1 | a0001 | c0003 | t0002 | g0190 | EAS | CHB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18747 | hp2 | a0001 | c0005 | t0001 | g0010 | EAS | CHB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18906 | hp2 | a0001 | c0007 | t0001 | g0021 | AFR | YRI | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18940 | hp1 | a0001 | c0006 | t0004 | g0004 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18942 | hp1 | a0012 | c0036 | t0001 | g0180 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18942 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18944 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18944 | hp2 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18946 | hp1 | a0001 | c0035 | t0001 | g0089 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18947 | hp1 | a0001 | c0005 | t0002 | g0166 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18947 | hp2 | a0001 | c0003 | t0001 | g0063 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18948 | hp2 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18949 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18953 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18953 | hp2 | a0001 | c0006 | t0004 | g0004 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0181 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18954 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18956 | hp1 | a0001 | c0007 | t0001 | g0182 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18961 | hp1 | a0001 | c0011 | t0003 | g0179 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18961 | hp2 | a0001 | c0006 | t0004 | g0004 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18964 | hp1 | a0001 | c0006 | t0004 | g0034 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18965 | hp2 | a0001 | c0006 | t0004 | g0004 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18966 | hp1 | a0001 | c0007 | t0001 | g0076 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18967 | hp2 | a0001 | c0003 | t0002 | g0057 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18969 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0233 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18974 | hp2 | a0001 | c0005 | t0001 | g0119 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18977 | hp1 | a0001 | c0005 | t0001 | g0010 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18978 | hp1 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18978 | hp2 | a0001 | c0006 | t0004 | g0077 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18979 | hp1 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18979 | hp2 | a0001 | c0006 | t0004 | g0004 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18980 | hp2 | a0001 | c0003 | t0003 | g0055 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18981 | hp1 | a0002 | c0010 | t0003 | g0019 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18981 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18982 | hp1 | a0001 | c0005 | t0002 | g0214 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18983 | hp1 | a0013 | c0032 | t0001 | g0095 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18983 | hp2 | a0001 | c0003 | t0002 | g0184 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18984 | hp1 | a0002 | c0004 | t0002 | g0018 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18985 | hp1 | a0001 | c0003 | t0004 | g0221 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18986 | hp1 | a0001 | c0005 | t0003 | g0033 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18986 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18987 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18987 | hp2 | a0001 | c0005 | t0001 | g0010 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18989 | hp1 | a0001 | c0003 | t0002 | g0057 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18989 | hp2 | a0001 | c0005 | t0001 | g0045 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18991 | hp1 | a0002 | c0004 | t0002 | g0018 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18991 | hp2 | a0001 | c0003 | t0001 | g0219 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18993 | hp1 | a0001 | c0003 | t0001 | g0063 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18997 | hp2 | a0014 | c0028 | t0002 | g0207 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18999 | hp1 | a0001 | c0005 | t0001 | g0135 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19000 | hp2 | a0001 | c0005 | t0003 | g0033 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19001 | hp1 | a0001 | c0006 | t0001 | g0015 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19001 | hp2 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0224 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19003 | hp2 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19006 | hp1 | a0002 | c0010 | t0003 | g0019 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0191 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19009 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19010 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19011 | hp2 | a0001 | c0005 | t0001 | g0044 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19030 | hp1 | a0001 | c0007 | t0001 | g0187 | AFR | LWK | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | LWK | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19043 | hp2 | a0001 | c0006 | t0004 | g0079 | AFR | LWK | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19054 | hp2 | a0001 | c0005 | t0001 | g0044 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19057 | hp1 | a0002 | c0004 | t0002 | g0018 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19057 | hp2 | a0001 | c0003 | t0003 | g0055 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19058 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19058 | hp2 | a0002 | c0004 | t0002 | g0018 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19060 | hp1 | a0001 | c0003 | t0002 | g0188 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19062 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19062 | hp2 | a0002 | c0010 | t0003 | g0019 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19064 | hp1 | a0004 | c0012 | t0001 | g0222 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19065 | hp2 | a0001 | c0006 | t0004 | g0004 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19067 | hp1 | a0001 | c0006 | t0001 | g0015 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19070 | hp1 | a0001 | c0006 | t0004 | g0078 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19070 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19072 | hp1 | a0001 | c0003 | t0001 | g0195 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19072 | hp2 | a0001 | c0006 | t0004 | g0034 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19074 | hp2 | a0001 | c0005 | t0001 | g0045 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19075 | hp2 | a0015 | c0023 | t0004 | g0004 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19079 | hp1 | a0001 | c0005 | t0001 | g0069 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19079 | hp2 | a0001 | c0006 | t0001 | g0015 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19080 | hp2 | a0001 | c0003 | t0001 | g0220 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19081 | hp1 | a0002 | c0004 | t0003 | g0019 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19081 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19082 | hp1 | a0001 | c0006 | t0004 | g0004 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19082 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19083 | hp1 | a0004 | c0012 | t0004 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19085 | hp2 | a0001 | c0005 | t0003 | g0007 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19090 | hp1 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19090 | hp2 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19091 | hp2 | a0001 | c0006 | t0001 | g0015 | EAS | JPT | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19240 | hp1 | a0003 | c0033 | t0001 | g0068 | AFR | YRI | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA19240 | hp2 | a0001 | c0008 | t0001 | g0005 | AFR | YRI | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA20129 | hp1 | a0001 | c0017 | t0006 | g0234 | AFR | ASW | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA20129 | hp2 | a0001 | c0009 | t0001 | g0073 | AFR | ASW | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA20752 | hp1 | a0002 | c0004 | t0002 | g0238 | EUR | TSI | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA20752 | hp2 | a0002 | c0004 | t0002 | g0154 | EUR | TSI | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA20805 | hp1 | a0002 | c0004 | t0003 | g0212 | EUR | TSI | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA20805 | hp2 | a0002 | c0004 | t0002 | g0136 | EUR | TSI | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA20905 | hp1 | a0001 | c0005 | t0003 | g0115 | SAS | GIH | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA20905 | hp2 | a0001 | c0005 | t0002 | g0121 | SAS | GIH | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01123 | hp1 | a0001 | c0006 | t0001 | g0024 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02109 | hp1 | a0001 | c0008 | t0001 | g0005 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02109 | hp2 | a0001 | c0009 | t0001 | g0162 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02486 | hp1 | a0001 | c0006 | t0001 | g0048 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02559 | hp1 | a0001 | c0007 | t0004 | g0193 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG06807 | hp1 | a0002 | c0004 | t0002 | g0157 | AFR | USA | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| HG06807 | hp2 | a0001 | c0009 | t0003 | g0244 | AFR | USA | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA20300 | hp1 | a0002 | c0004 | t0002 | g0012 | AFR | USA | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA20300 | hp2 | a0002 | c0026 | t0001 | g0163 | AFR | USA | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA21309 | hp1 | a0001 | c0009 | t0003 | g0243 | AFR | LWK | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| NA21309 | hp2 | a0001 | c0021 | t0001 | g0138 | AFR | LWK | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0208 | REF | REF | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| homoSapiens | grch38p0 | a0002 | c0004 | t0003 | g0020 | REF | REF | COL1A2_chr7_94389895_94436227 | COL1A2 | chr7 | 94389895 | 94436227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:94400218 | G | C | 1 | a0008 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.155G>C | p.Arg52Thr | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 5/52 | 292/5072 | 155/4101 | 52/1366 | chr7 | 94400218 | |||
| chr7:94410254 | C | T | 1 | a0012 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.1048C>T | p.Pro350Ser | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 20/52 | 1185/5072 | 1048/4101 | 350/1366 | chr7 | 94410254 | |||
| chr7:94413115 | T | G | 1 | a0004 | 2 | NA19064.hp1 NA19083.hp1 |
missense_variant | MODERATE | c.1536T>G | p.His512Gln | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 26/52 | 1673/5072 | 1536/4101 | 512/1366 | chr7 | 94413115 | |||
| chr7:94413742 | A | G | 1 | a0015 | 1 | NA19075.hp2 | missense_variant&splice_region_variant | MODERATE | c.1610A>G | p.Gln537Arg | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 27/52 | 1747/5072 | 1610/4101 | 537/1366 | chr7 | 94413742 | |||
| chr7:94413927 | C | G | 13 | a0001 a0003 a0004 others(10): Show |
378 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(375): Show |
missense_variant | MODERATE | c.1645C>G | p.Pro549Ala | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 28/52 | 1782/5072 | 1645/4101 | 549/1366 | chr7 | 94413927 | |||
| chr7:94419550 | G | A | 1 | a0005 | 1 | HG00323.hp1 | missense_variant&splice_region_variant | MODERATE | c.2078G>A | p.Arg693Gln | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 34/52 | 2215/5072 | 2078/4101 | 693/1366 | chr7 | 94419550 | |||
| chr7:94423041 | C | T | 1 | a0009 | 1 | HG03017.hp1 | stop_gained | HIGH | c.2488C>T | p.Arg830* | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/52 | 2625/5072 | 2488/4101 | 830/1366 | chr7 | 94423041 | |||
| chr7:94425775 | T | C | 1 | a0011 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.2861T>C | p.Ile954Thr | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 44/52 | 2998/5072 | 2861/4101 | 954/1366 | chr7 | 94425775 | |||
| chr7:94425847 | G | A | 1 | a0007 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.2933G>A | p.Arg978His | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 44/52 | 3070/5072 | 2933/4101 | 978/1366 | chr7 | 94425847 | |||
| chr7:94427041 | G | A | 1 | a0010 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.3139G>A | p.Val1047Met | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 47/52 | 3276/5072 | 3139/4101 | 1047/1366 | chr7 | 94427041 | |||
| chr7:94427672 | G | A | 1 | a0013 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.3313G>A | p.Gly1105Ser | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 49/52 | 3450/5072 | 3313/4101 | 1105/1366 | chr7 | 94427672 | |||
| chr7:94428380 | G | A | 1 | a0003 | 3 | HG01243.hp2 HG02818.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.3614G>A | p.Arg1205Gln | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 50/52 | 3751/5072 | 3614/4101 | 1205/1366 | chr7 | 94428380 | |||
| chr7:94429215 | TCCAAGGA others(6): Show |
T | 1 | a0014 | 1 | NA18997.hp2 | frameshift_variant | HIGH | c.3740_3752delCCAAGG others(7): Show |
p.Ser1247fs | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/52 | 3877/5072 | 3740/4101 | 1247/1366 | chr7 | 94429215 | |||
| chr7:94429274 | G | T | 1 | a0014 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.3798G>T | p.Gln1266His | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/52 | 3935/5072 | 3798/4101 | 1266/1366 | chr7 | 94429274 | |||
| chr7:94429287 | C | A | 1 | a0014 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.3811C>A | p.His1271Asn | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/52 | 3948/5072 | 3811/4101 | 1271/1366 | chr7 | 94429287 | |||
| chr7:94429291 | G | A | 1 | a0014 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.3815G>A | p.Cys1272Tyr | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/52 | 3952/5072 | 3815/4101 | 1272/1366 | chr7 | 94429291 | |||
| chr7:94429301 | C | A | 1 | a0014 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.3825C>A | p.Ser1275Arg | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/52 | 3962/5072 | 3825/4101 | 1275/1366 | chr7 | 94429301 | |||
| chr7:94429305 | G | C | 1 | a0014 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.3829G>C | p.Ala1277Pro | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/52 | 3966/5072 | 3829/4101 | 1277/1366 | chr7 | 94429305 | |||
| chr7:94429306 | C | A | 1 | a0014 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.3830C>A | p.Ala1277Glu | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/52 | 3967/5072 | 3830/4101 | 1277/1366 | chr7 | 94429306 | |||
| chr7:94429316 | T | G | 1 | a0014 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.3840T>G | p.Asp1280Glu | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/52 | 3977/5072 | 3840/4101 | 1280/1366 | chr7 | 94429316 | |||
| chr7:94429317 | G | A | 1 | a0014 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.3841G>A | p.Glu1281Lys | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/52 | 3978/5072 | 3841/4101 | 1281/1366 | chr7 | 94429317 | |||
| chr7:94429322 | G | T | 1 | a0014 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.3846G>T | p.Glu1282Asp | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/52 | 3983/5072 | 3846/4101 | 1282/1366 | chr7 | 94429322 | |||
| chr7:94429327 | G | T | 1 | a0014 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.3851G>T | p.Gly1284Val | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/52 | 3988/5072 | 3851/4101 | 1284/1366 | chr7 | 94429327 | |||
| chr7:94429342 | C | G | 1 | a0006 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.3866C>G | p.Ala1289Gly | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/52 | 4003/5072 | 3866/4101 | 1289/1366 | chr7 | 94429342 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:94398387 | T | C | 7 | a0001c0003 a0001c0007 a0001c0008 others(4): Show |
106 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(103): Show |
synonymous_variant | LOW | c.87T>C | p.Thr29Thr | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 3/52 | 224/5072 | 87/4101 | 29/1366 | chr7 | 94398387 | |||
| chr7:94401587 | T | C | 15 | a0001c0003 a0001c0006 a0001c0007 others(12): Show |
154 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(151): Show |
synonymous_variant | LOW | c.246T>C | p.Asp82Asp | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/52 | 383/5072 | 246/4101 | 82/1366 | chr7 | 94401587 | |||
| chr7:94408814 | T | C | 1 | a0002c0010 | 3 | NA18981.hp1 NA19006.hp1 NA19062.hp2 |
synonymous_variant | LOW | c.783T>C | p.Pro261Pro | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 16/52 | 920/5072 | 783/4101 | 261/1366 | chr7 | 94408814 | |||
| chr7:94409767 | C | T | 1 | a0001c0037 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.981C>T | p.Arg327Arg | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 19/52 | 1118/5072 | 981/4101 | 327/1366 | chr7 | 94409767 | |||
| chr7:94412100 | C | T | 1 | a0001c0024 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.1383C>T | p.Pro461Pro | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 24/52 | 1520/5072 | 1383/4101 | 461/1366 | chr7 | 94412100 | |||
| chr7:94412625 | A | C | 15 | a0001c0002 a0001c0006 a0001c0008 others(12): Show |
140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
synonymous_variant | LOW | c.1446A>C | p.Pro482Pro | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 25/52 | 1583/5072 | 1446/4101 | 482/1366 | chr7 | 94412625 | |||
| chr7:94417738 | G | T | 5 | a0001c0003 a0001c0011 a0001c0035 others(2): Show |
77 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(74): Show |
synonymous_variant | LOW | c.1878G>T | p.Val626Val | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 32/52 | 2015/5072 | 1878/4101 | 626/1366 | chr7 | 94417738 | |||
| chr7:94425143 | C | T | 1 | a0001c0015 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.2700C>T | p.Ala900Ala | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 42/52 | 2837/5072 | 2700/4101 | 900/1366 | chr7 | 94425143 | |||
| chr7:94426443 | C | T | 1 | a0001c0022 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.3018C>T | p.Gly1006Gly | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 46/52 | 3155/5072 | 3018/4101 | 1006/1366 | chr7 | 94426443 | |||
| chr7:94427037 | C | T | 7 | a0001c0005 a0001c0014 a0001c0017 others(4): Show |
45 | HG00558.hp1 HG00621.hp1 HG01175.hp1 others(42): Show |
synonymous_variant | LOW | c.3135C>T | p.Gly1045Gly | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 47/52 | 3272/5072 | 3135/4101 | 1045/1366 | chr7 | 94427037 | |||
| chr7:94427695 | C | T | 2 | a0001c0029 a0002c0026 |
2 | HG03225.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.3336C>T | p.Tyr1112Tyr | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 49/52 | 3473/5072 | 3336/4101 | 1112/1366 | chr7 | 94427695 | |||
| chr7:94428351 | T | C | 1 | a0001c0024 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.3585T>C | p.Cys1195Cys | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 50/52 | 3722/5072 | 3585/4101 | 1195/1366 | chr7 | 94428351 | |||
| chr7:94429307 | A | G | 1 | a0014c0028 | 1 | NA18997.hp2 | synonymous_variant | LOW | c.3831A>G | p.Ala1277Ala | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/52 | 3968/5072 | 3831/4101 | 1277/1366 | chr7 | 94429307 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:94430587 | C | T | 9 | a0001c0001t0002 a0001c0002t0002 a0001c0003t0002 others(6): Show |
93 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*194C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 52/52 | 194 | chr7 | 94430587 | ||||||
| chr7:94430598 | A | G | 3 | a0001c0001t0005 a0001c0007t0005 a0001c0015t0005 |
6 | HG02145.hp2 HG02615.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*205A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 52/52 | 205 | chr7 | 94430598 | ||||||
| chr7:94430676 | T | C | 2 | a0001c0002t0006 a0001c0017t0006 |
2 | HG01891.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*283T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 52/52 | 283 | chr7 | 94430676 | ||||||
| chr7:94430808 | T | G | 1 | a0001c0029t0007 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*415T>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 52/52 | 415 | chr7 | 94430808 | ||||||
| chr7:94431047 | A | AGTTGTCC | 52 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(49): Show |
374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
3_prime_UTR_variant | MODIFIER | c.*654_*655insGTTGTC others(1): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 52/52 | 655 | chr7 | 94431047 | ||||||
| chr7:94431197 | G | T | 8 | a0001c0001t0004 a0001c0002t0004 a0001c0003t0004 others(5): Show |
29 | HG00438.hp2 HG00735.hp1 HG01069.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*804G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 52/52 | 804 | chr7 | 94431197 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:94395346 | G | A | 2 | a0003c0013t0001g0065 a0003c0013t0001g0066 |
2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.70+245G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94395346 | |||||||
| chr7:94395380 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.70+279G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94395380 | |||||||
| chr7:94395591 | G | T | 1 | a0001c0002t0001g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.70+490G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94395591 | |||||||
| chr7:94395594 | T | C | 1 | a0001c0002t0001g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.70+493T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94395594 | |||||||
| chr7:94395619 | A | G | 6 | a0001c0009t0003g0241 a0001c0009t0003g0243 a0001c0009t0003g0244 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.70+518A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94395619 | |||||||
| chr7:94395640 | G | C | 1 | a0003c0033t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.70+539G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94395640 | |||||||
| chr7:94395760 | G | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0240 |
5 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+659G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94395760 | |||||||
| chr7:94395819 | TAA | T | 4 | a0002c0004t0001g0064 a0002c0004t0002g0238 a0002c0004t0003g0239 others(1): Show |
4 | HG02698.hp1 HG03834.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+719_70+720delAA | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94395819 | |||||||
| chr7:94395840 | T | G | 1 | a0001c0005t0001g0069 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.70+739T>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94395840 | |||||||
| chr7:94395942 | A | T | 1 | a0001c0001t0003g0237 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.70+841A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94395942 | |||||||
| chr7:94396039 | G | A | 1 | a0001c0001t0001g0014 | 4 | HG01358.hp2 HG01928.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+938G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94396039 | |||||||
| chr7:94396145 | TGAA | T | 1 | a0001c0002t0003g0031 | 3 | HG01256.hp2 HG01258.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.70+1050_70+1052del others(3): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr7 | 94396145 | ||||||
| chr7:94396213 | T | C | 1 | a0002c0004t0002g0070 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.70+1112T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94396213 | |||||||
| chr7:94396248 | C | A | 1 | a0001c0003t0001g0071 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.70+1147C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94396248 | |||||||
| chr7:94396251 | A | T | 1 | a0006c0016t0001g0236 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.70+1150A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94396251 | |||||||
| chr7:94396314 | T | TTG | 20 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(17): Show |
27 | HG00741.hp2 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.70+1241_70+1242dup others(2): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr7 | 94396314 | ||||||
| chr7:94396314 | T | TTGTG | 17 | a0001c0001t0001g0029 a0001c0001t0001g0171 a0001c0001t0002g0053 others(14): Show |
20 | HG02015.hp2 HG02922.hp2 HG02970.hp2 others(17): Show |
intron_variant | MODIFIER | c.70+1239_70+1242dup others(4): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr7 | 94396314 | ||||||
| chr7:94396314 | T | TTGTGTG | 68 | a0001c0001t0001g0022 a0001c0001t0001g0058 a0001c0001t0001g0067 others(65): Show |
126 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.70+1237_70+1242dup others(6): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr7 | 94396314 | ||||||
| chr7:94396314 | T | TTGTGTGT others(1): Show |
6 | a0001c0001t0001g0062 a0001c0003t0001g0233 a0001c0003t0002g0008 others(3): Show |
13 | HG00621.hp2 HG01943.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.70+1235_70+1242dup others(8): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr7 | 94396314 | ||||||
| chr7:94396314 | T | TTGTGTGT others(3): Show |
3 | a0001c0001t0002g0235 a0001c0003t0001g0063 a0001c0017t0006g0234 |
4 | HG02135.hp2 NA18947.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+1233_70+1242dup others(10): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr7 | 94396314 | ||||||
| chr7:94396314 | TTG | T | 7 | a0001c0005t0001g0135 a0001c0006t0001g0048 a0001c0006t0002g0134 others(4): Show |
8 | HG01109.hp2 HG02071.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.70+1241_70+1242del others(2): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr7 | 94396314 | ||||||
| chr7:94396314 | TTGTG | T | 92 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0042 others(89): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.70+1239_70+1242del others(4): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr7 | 94396314 | ||||||
| chr7:94396314 | TTGTGTG | T | 2 | a0001c0005t0001g0074 a0001c0005t0003g0033 |
3 | HG03927.hp1 NA18986.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.70+1237_70+1242del others(6): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr7 | 94396314 | ||||||
| chr7:94396314 | TTGTGTGT others(1): Show |
T | 2 | a0001c0002t0001g0072 a0001c0006t0004g0032 |
3 | HG01069.hp1 HG01070.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.70+1235_70+1242del others(8): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr7 | 94396314 | ||||||
| chr7:94396336 | G | C | 1 | a0001c0009t0001g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.70+1235G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94396336 | |||||||
| chr7:94396359 | T | G | 1 | a0002c0004t0002g0136 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.70+1258T>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94396359 | |||||||
| chr7:94396377 | A | C | 11 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
15 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.70+1276A>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94396377 | |||||||
| chr7:94396398 | G | A | 7 | a0001c0001t0001g0029 a0001c0001t0001g0159 a0001c0001t0001g0171 others(4): Show |
8 | HG00741.hp2 HG02922.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+1297G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94396398 | |||||||
| chr7:94396425 | A | G | 24 | a0001c0003t0001g0003 a0001c0003t0001g0006 a0001c0003t0001g0030 others(21): Show |
50 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.71-1323A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94396425 | |||||||
| chr7:94396463 | G | C | 1 | a0001c0006t0001g0048 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.71-1285G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94396463 | |||||||
| chr7:94396505 | G | C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.71-1243G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94396505 | |||||||
| chr7:94396612 | A | G | 132 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0022 others(129): Show |
218 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.71-1136A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94396612 | |||||||
| chr7:94396866 | G | A | 1 | a0001c0001t0005g0082 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-882G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94396866 | |||||||
| chr7:94396927 | TACCGTAG others(11): Show |
T | 1 | a0001c0006t0002g0081 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.71-818_71-801delCG others(16): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr7 | 94396927 | ||||||
| chr7:94396984 | G | C | 1 | a0001c0003t0002g0184 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.71-764G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94396984 | |||||||
| chr7:94397150 | CCATTTTC others(37): Show |
C | 1 | a0001c0006t0002g0081 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.71-597_71-554delCA others(42): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397150 | |||||||
| chr7:94397195 | G | A | 1 | a0001c0006t0002g0081 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.71-553G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397195 | |||||||
| chr7:94397219 | A | G | 3 | a0002c0004t0002g0012 a0002c0004t0002g0050 a0002c0004t0002g0158 |
8 | HG01081.hp2 HG02683.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-529A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397219 | |||||||
| chr7:94397270 | T | A | 9 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.71-478T>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397270 | |||||||
| chr7:94397292 | A | G | 1 | a0003c0033t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.71-456A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397292 | |||||||
| chr7:94397307 | G | A | 1 | a0001c0002t0001g0083 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.71-441G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397307 | |||||||
| chr7:94397320 | C | T | 3 | a0002c0004t0002g0028 a0002c0004t0002g0157 a0002c0004t0003g0028 |
4 | HG00280.hp1 HG00323.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-428C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397320 | |||||||
| chr7:94397363 | A | T | 9 | a0001c0001t0001g0029 a0001c0001t0001g0159 a0001c0001t0001g0171 others(6): Show |
10 | HG00741.hp2 HG01243.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.71-385A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397363 | |||||||
| chr7:94397390 | C | T | 34 | a0001c0001t0001g0022 a0001c0001t0001g0058 a0001c0001t0001g0062 others(31): Show |
56 | HG00597.hp1 HG00673.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.71-358C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397390 | |||||||
| chr7:94397416 | T | C | 2 | a0001c0009t0001g0162 a0001c0022t0001g0161 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.71-332T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397416 | |||||||
| chr7:94397498 | T | C | 2 | a0001c0009t0001g0162 a0001c0022t0001g0161 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.71-250T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397498 | |||||||
| chr7:94397550 | A | T | 1 | a0001c0006t0001g0232 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.71-198A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397550 | |||||||
| chr7:94397586 | G | A | 1 | a0001c0009t0001g0137 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.71-162G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397586 | |||||||
| chr7:94397669 | T | A | 1 | a0001c0003t0001g0071 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.71-79T>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397669 | |||||||
| chr7:94397731 | C | CT | 17 | a0001c0006t0001g0015 a0001c0006t0001g0024 a0001c0006t0002g0035 others(14): Show |
34 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(31): Show |
splice_region_variant&intron_variant | LOW | c.71-7dupT | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr7 | 94397731 | ||||||
| chr7:94397742 | C | T | 1 | a0001c0003t0001g0230 | 1 | NA19003.hp2 | splice_region_variant&intron_variant | LOW | c.71-6C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 1/51 | chr7 | 94397742 | |||||||
| chr7:94397813 | G | A | 1 | a0001c0006t0001g0048 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.81+55G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 2/51 | chr7 | 94397813 | |||||||
| chr7:94397860 | C | T | 1 | a0001c0005t0001g0129 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.81+102C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 2/51 | chr7 | 94397860 | |||||||
| chr7:94397931 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.81+173C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 2/51 | chr7 | 94397931 | |||||||
| chr7:94398137 | G | A | 9 | a0001c0001t0001g0029 a0001c0001t0001g0159 a0001c0001t0001g0171 others(6): Show |
10 | HG00741.hp2 HG01243.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.82-245G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 2/51 | chr7 | 94398137 | |||||||
| chr7:94398196 | C | T | 2 | a0001c0009t0001g0162 a0001c0022t0001g0161 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.82-186C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 2/51 | chr7 | 94398196 | |||||||
| chr7:94398219 | T | C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.82-163T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 2/51 | chr7 | 94398219 | |||||||
| chr7:94398370 | A | G | 6 | a0001c0009t0003g0241 a0001c0009t0003g0243 a0001c0009t0003g0244 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-12A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 2/51 | chr7 | 94398370 | |||||||
| chr7:94398406 | C | T | 2 | a0003c0013t0001g0065 a0003c0013t0001g0066 |
2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.96+10C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 3/51 | chr7 | 94398406 | |||||||
| chr7:94398456 | T | A | 1 | a0001c0007t0004g0185 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.96+60T>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 3/51 | chr7 | 94398456 | |||||||
| chr7:94398508 | A | G | 2 | a0001c0003t0002g0057 a0001c0003t0002g0184 |
3 | NA18967.hp2 NA18983.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.96+112A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 3/51 | chr7 | 94398508 | |||||||
| chr7:94398634 | AG | A | 9 | a0001c0001t0001g0029 a0001c0001t0001g0159 a0001c0001t0001g0171 others(6): Show |
10 | HG00741.hp2 HG01243.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.96+240delG | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 3/51 | INFO_REALIGN_3_PRIME | chr7 | 94398634 | ||||||
| chr7:94398636 | GA | G | 9 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+249delA | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 3/51 | INFO_REALIGN_3_PRIME | chr7 | 94398636 | ||||||
| chr7:94398826 | G | C | 1 | a0001c0002t0006g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.97-223G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 3/51 | chr7 | 94398826 | |||||||
| chr7:94398930 | C | G | 2 | a0001c0003t0001g0229 a0001c0003t0001g0233 |
2 | NA18971.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.97-119C>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 3/51 | chr7 | 94398930 | |||||||
| chr7:94398983 | T | C | 1 | a0001c0022t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97-66T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 3/51 | chr7 | 94398983 | |||||||
| chr7:94399115 | G | A | 44 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(41): Show |
84 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.132+31G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 4/51 | chr7 | 94399115 | |||||||
| chr7:94399280 | C | T | 2 | a0001c0001t0004g0172 a0001c0002t0001g0173 |
2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.132+196C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 4/51 | chr7 | 94399280 | |||||||
| chr7:94399485 | C | G | 9 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.132+401C>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 4/51 | chr7 | 94399485 | |||||||
| chr7:94399612 | A | G | 80 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0042 others(77): Show |
139 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.132+528A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 4/51 | chr7 | 94399612 | |||||||
| chr7:94399847 | G | A | 2 | a0001c0006t0001g0048 a0001c0021t0001g0138 |
3 | HG02486.hp1 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.133-349G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 4/51 | chr7 | 94399847 | |||||||
| chr7:94399883 | T | A | 1 | a0003c0033t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.133-313T>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 4/51 | chr7 | 94399883 | |||||||
| chr7:94400006 | A | G | 1 | a0001c0024t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.133-190A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 4/51 | chr7 | 94400006 | |||||||
| chr7:94400041 | C | T | 2 | a0003c0013t0001g0065 a0003c0013t0001g0066 |
2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.133-155C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 4/51 | chr7 | 94400041 | |||||||
| chr7:94400169 | T | C | 1 | a0001c0001t0003g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.133-27T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 4/51 | chr7 | 94400169 | |||||||
| chr7:94400497 | C | T | 9 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.225+209C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 5/51 | chr7 | 94400497 | |||||||
| chr7:94400670 | C | T | 56 | a0001c0003t0001g0003 a0001c0003t0001g0006 a0001c0003t0001g0013 others(53): Show |
105 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.225+382C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 5/51 | chr7 | 94400670 | |||||||
| chr7:94400855 | A | G | 80 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0042 others(77): Show |
139 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.225+567A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 5/51 | chr7 | 94400855 | |||||||
| chr7:94401034 | G | C | 80 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0042 others(77): Show |
139 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.226-533G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 5/51 | chr7 | 94401034 | |||||||
| chr7:94401310 | G | A | 1 | a0003c0033t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.226-257G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 5/51 | chr7 | 94401310 | |||||||
| chr7:94401345 | A | G | 9 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.226-222A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 5/51 | chr7 | 94401345 | |||||||
| chr7:94401544 | A | AT | 58 | a0001c0002t0001g0105 a0001c0003t0001g0003 a0001c0003t0001g0006 others(55): Show |
107 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.226-11dupT | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 5/51 | INFO_REALIGN_3_PRIME | chr7 | 94401544 | ||||||
| chr7:94401753 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.279+133T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94401753 | |||||||
| chr7:94401769 | T | C | 1 | a0001c0005t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.279+149T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94401769 | |||||||
| chr7:94401834 | A | T | 2 | a0003c0013t0001g0065 a0003c0013t0001g0066 |
2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.279+214A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94401834 | |||||||
| chr7:94401948 | G | T | 1 | a0001c0002t0001g0128 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.279+328G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94401948 | |||||||
| chr7:94402001 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.279+381G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94402001 | |||||||
| chr7:94402022 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.279+402C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94402022 | |||||||
| chr7:94402125 | C | T | 2 | a0001c0001t0001g0052 a0010c0027t0001g0052 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.279+505C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94402125 | |||||||
| chr7:94402145 | T | G | 80 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0042 others(77): Show |
139 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.279+525T>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94402145 | |||||||
| chr7:94402166 | C | G | 1 | a0012c0036t0001g0180 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.279+546C>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94402166 | |||||||
| chr7:94402281 | G | C | 1 | a0001c0029t0007g0168 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.279+661G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94402281 | |||||||
| chr7:94402493 | G | A | 58 | a0001c0003t0001g0003 a0001c0003t0001g0006 a0001c0003t0001g0013 others(55): Show |
107 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.279+873G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94402493 | |||||||
| chr7:94402645 | C | G | 1 | a0001c0001t0002g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.279+1025C>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94402645 | |||||||
| chr7:94402703 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.279+1083C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94402703 | |||||||
| chr7:94402779 | G | A | 1 | a0001c0006t0004g0077 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.279+1159G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94402779 | |||||||
| chr7:94402793 | G | A | 34 | a0001c0001t0001g0022 a0001c0001t0001g0058 a0001c0001t0001g0062 others(31): Show |
56 | HG00597.hp1 HG00673.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.279+1173G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94402793 | |||||||
| chr7:94402900 | A | G | 15 | a0001c0006t0001g0015 a0001c0006t0001g0024 a0001c0006t0002g0035 others(12): Show |
32 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.279+1280A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94402900 | |||||||
| chr7:94402973 | A | G | 9 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.279+1353A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94402973 | |||||||
| chr7:94402979 | A | T | 1 | a0001c0003t0001g0071 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.279+1359A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94402979 | |||||||
| chr7:94403013 | G | A | 35 | a0001c0001t0001g0088 a0001c0002t0001g0001 a0001c0002t0001g0017 others(32): Show |
71 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.279+1393G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403013 | |||||||
| chr7:94403114 | G | A | 1 | a0001c0006t0001g0232 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.280-1442G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403114 | |||||||
| chr7:94403174 | A | G | 1 | a0001c0017t0006g0234 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.280-1382A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403174 | |||||||
| chr7:94403198 | C | G | 2 | a0001c0009t0001g0073 a0001c0009t0001g0137 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.280-1358C>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403198 | |||||||
| chr7:94403198 | C | T | 1 | a0001c0008t0001g0061 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.280-1358C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403198 | |||||||
| chr7:94403309 | T | C | 1 | a0001c0002t0001g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.280-1247T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403309 | |||||||
| chr7:94403398 | T | C | 1 | a0003c0033t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.280-1158T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403398 | |||||||
| chr7:94403441 | A | G | 80 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0042 others(77): Show |
139 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.280-1115A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403441 | |||||||
| chr7:94403462 | A | T | 2 | a0001c0009t0001g0162 a0001c0022t0001g0161 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.280-1094A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403462 | |||||||
| chr7:94403476 | A | G | 1 | a0001c0003t0003g0199 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.280-1080A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403476 | |||||||
| chr7:94403613 | C | A | 7 | a0001c0001t0001g0029 a0001c0001t0001g0159 a0001c0001t0001g0171 others(4): Show |
8 | HG00741.hp2 HG02922.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.280-943C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403613 | |||||||
| chr7:94403630 | A | G | 123 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0022 others(120): Show |
208 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.280-926A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403630 | |||||||
| chr7:94403631 | T | C | 1 | a0001c0024t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.280-925T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403631 | |||||||
| chr7:94403648 | C | T | 1 | a0001c0024t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.280-908C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403648 | |||||||
| chr7:94403676 | C | A | 3 | a0001c0009t0001g0073 a0001c0009t0001g0137 a0001c0009t0001g0139 |
3 | HG00738.hp1 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.280-880C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403676 | |||||||
| chr7:94403719 | T | C | 123 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0022 others(120): Show |
208 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.280-837T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403719 | |||||||
| chr7:94403779 | A | G | 7 | a0001c0001t0001g0029 a0001c0001t0001g0159 a0001c0001t0001g0171 others(4): Show |
8 | HG00741.hp2 HG02922.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.280-777A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403779 | |||||||
| chr7:94403800 | C | T | 219 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0022 others(216): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(369): Show |
intron_variant | MODIFIER | c.280-756C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403800 | |||||||
| chr7:94403996 | C | T | 1 | a0001c0001t0004g0126 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.280-560C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94403996 | |||||||
| chr7:94404025 | T | G | 37 | a0001c0001t0001g0088 a0001c0002t0001g0001 a0001c0002t0001g0017 others(34): Show |
73 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.280-531T>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94404025 | |||||||
| chr7:94404204 | C | A | 1 | a0003c0033t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.280-352C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94404204 | |||||||
| chr7:94404208 | C | T | 1 | a0001c0024t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.280-348C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94404208 | |||||||
| chr7:94404236 | A | G | 1 | a0002c0004t0002g0154 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.280-320A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94404236 | |||||||
| chr7:94404300 | T | C | 7 | a0001c0003t0002g0008 a0001c0003t0002g0057 a0001c0003t0002g0184 others(4): Show |
14 | HG00621.hp2 HG02040.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.280-256T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94404300 | |||||||
| chr7:94404360 | A | T | 44 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0051 others(41): Show |
70 | HG00597.hp1 HG00673.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.280-196A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94404360 | |||||||
| chr7:94404454 | C | A | 1 | a0001c0003t0001g0219 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.280-102C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94404454 | |||||||
| chr7:94404488 | A | G | 43 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0051 others(40): Show |
69 | HG00597.hp1 HG00673.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.280-68A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 6/51 | chr7 | 94404488 | |||||||
| chr7:94404953 | T | G | 1 | a0001c0008t0001g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.432+61T>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 9/51 | chr7 | 94404953 | |||||||
| chr7:94405028 | A | T | 1 | a0002c0004t0003g0153 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.432+136A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 9/51 | chr7 | 94405028 | |||||||
| chr7:94405049 | A | C | 1 | a0003c0033t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.433-150A>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 9/51 | chr7 | 94405049 | |||||||
| chr7:94405107 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.433-92A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 9/51 | chr7 | 94405107 | |||||||
| chr7:94405348 | C | T | 1 | a0002c0019t0001g0246 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.486+96C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 10/51 | chr7 | 94405348 | |||||||
| chr7:94405377 | C | T | 58 | a0001c0003t0001g0003 a0001c0003t0001g0006 a0001c0003t0001g0013 others(55): Show |
107 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.486+125C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 10/51 | chr7 | 94405377 | |||||||
| chr7:94405385 | G | T | 1 | a0002c0004t0002g0152 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.486+133G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 10/51 | chr7 | 94405385 | |||||||
| chr7:94405529 | A | G | 7 | a0001c0001t0001g0029 a0001c0001t0001g0159 a0001c0001t0001g0171 others(4): Show |
8 | HG00741.hp2 HG02922.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-144A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 10/51 | chr7 | 94405529 | |||||||
| chr7:94405536 | A | G | 44 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0051 others(41): Show |
70 | HG00597.hp1 HG00673.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.487-137A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 10/51 | chr7 | 94405536 | |||||||
| chr7:94405553 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.487-120A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 10/51 | chr7 | 94405553 | |||||||
| chr7:94405622 | T | C | 1 | a0001c0024t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.487-51T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 10/51 | chr7 | 94405622 | |||||||
| chr7:94405820 | T | A | 1 | a0001c0003t0002g0190 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.540+94T>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 11/51 | chr7 | 94405820 | |||||||
| chr7:94405920 | C | A | 1 | a0001c0002t0001g0086 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.540+194C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 11/51 | chr7 | 94405920 | |||||||
| chr7:94405986 | G | A | 2 | a0001c0006t0001g0048 a0001c0021t0001g0138 |
3 | HG02486.hp1 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.540+260G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 11/51 | chr7 | 94405986 | |||||||
| chr7:94406050 | T | C | 1 | a0001c0002t0001g0086 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.541-200T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 11/51 | chr7 | 94406050 | |||||||
| chr7:94406051 | C | T | 1 | a0001c0002t0001g0086 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.541-199C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 11/51 | chr7 | 94406051 | |||||||
| chr7:94406106 | C | T | 1 | a0001c0005t0001g0125 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.541-144C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 11/51 | chr7 | 94406106 | |||||||
| chr7:94406121 | C | T | 8 | a0001c0006t0001g0024 a0001c0006t0002g0035 a0001c0006t0002g0080 others(5): Show |
14 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.541-129C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 11/51 | chr7 | 94406121 | |||||||
| chr7:94406164 | G | T | 1 | a0003c0033t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.541-86G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 11/51 | chr7 | 94406164 | |||||||
| chr7:94406520 | A | G | 1 | a0001c0001t0002g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.594+217A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 12/51 | chr7 | 94406520 | |||||||
| chr7:94406580 | C | T | 89 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0029 others(86): Show |
149 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.594+277C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 12/51 | chr7 | 94406580 | |||||||
| chr7:94406692 | G | A | 1 | a0002c0004t0001g0140 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.594+389G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 12/51 | chr7 | 94406692 | |||||||
| chr7:94407235 | C | T | 134 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(131): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.595-612C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 12/51 | chr7 | 94407235 | |||||||
| chr7:94407343 | C | CACTACT | 51 | a0001c0001t0001g0022 a0001c0001t0001g0029 a0001c0001t0001g0051 others(48): Show |
75 | HG00673.hp1 HG00733.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.595-489_595-484dup others(6): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 12/51 | INFO_REALIGN_3_PRIME | chr7 | 94407343 | ||||||
| chr7:94407343 | C | CACTACTA others(2): Show |
141 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(138): Show |
248 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.595-492_595-484dup others(9): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 12/51 | INFO_REALIGN_3_PRIME | chr7 | 94407343 | ||||||
| chr7:94407343 | C | CACTACTA others(5): Show |
17 | a0001c0002t0003g0104 a0001c0002t0004g0124 a0001c0006t0001g0015 others(14): Show |
34 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.595-495_595-484dup others(12): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 12/51 | INFO_REALIGN_3_PRIME | chr7 | 94407343 | ||||||
| chr7:94407350 | A | ACTACTAC others(5): Show |
9 | a0001c0006t0001g0048 a0001c0008t0001g0005 a0001c0008t0001g0061 others(6): Show |
18 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.595-486_595-485ins others(12): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 12/51 | INFO_REALIGN_3_PRIME | chr7 | 94407350 | ||||||
| chr7:94407361 | T | TACTACTA others(5): Show |
1 | a0001c0024t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.595-484_595-483ins others(12): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 12/51 | INFO_REALIGN_3_PRIME | chr7 | 94407361 | ||||||
| chr7:94407414 | T | C | 1 | a0001c0009t0001g0139 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.595-433T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 12/51 | chr7 | 94407414 | |||||||
| chr7:94407479 | T | A | 1 | a0001c0001t0002g0176 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.595-368T>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 12/51 | chr7 | 94407479 | |||||||
| chr7:94407722 | A | G | 42 | a0001c0001t0001g0088 a0001c0002t0001g0001 a0001c0002t0001g0017 others(39): Show |
83 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.595-125A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 12/51 | chr7 | 94407722 | |||||||
| chr7:94407827 | C | T | 2 | a0003c0013t0001g0065 a0003c0013t0001g0066 |
2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.595-20C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 12/51 | chr7 | 94407827 | |||||||
| chr7:94407945 | G | A | 1 | a0001c0003t0001g0220 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.639+54G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 13/51 | chr7 | 94407945 | |||||||
| chr7:94407960 | T | C | 2 | a0003c0013t0001g0065 a0003c0013t0001g0066 |
2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.639+69T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 13/51 | chr7 | 94407960 | |||||||
| chr7:94408120 | T | C | 1 | a0001c0009t0003g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.640-63T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 13/51 | chr7 | 94408120 | |||||||
| chr7:94408276 | A | C | 1 | a0001c0003t0001g0183 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.693+40A>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 14/51 | chr7 | 94408276 | |||||||
| chr7:94408423 | G | T | 1 | a0001c0005t0002g0047 | 2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.738+43G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 15/51 | chr7 | 94408423 | |||||||
| chr7:94408466 | T | A | 16 | a0001c0002t0003g0104 a0001c0002t0004g0124 a0001c0006t0001g0015 others(13): Show |
33 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.738+86T>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 15/51 | chr7 | 94408466 | |||||||
| chr7:94408474 | GA | G | 3 | a0001c0002t0001g0211 a0001c0014t0002g0210 a0001c0017t0006g0234 |
3 | HG03209.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.738+95delA | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 15/51 | chr7 | 94408474 | |||||||
| chr7:94408478 | C | A | 16 | a0001c0002t0003g0104 a0001c0002t0004g0124 a0001c0006t0001g0015 others(13): Show |
33 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.738+98C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 15/51 | chr7 | 94408478 | |||||||
| chr7:94408581 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.739-189C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 15/51 | chr7 | 94408581 | |||||||
| chr7:94408597 | T | C | 1 | a0001c0001t0002g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.739-173T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 15/51 | chr7 | 94408597 | |||||||
| chr7:94408705 | C | T | 1 | a0003c0033t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.739-65C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 15/51 | chr7 | 94408705 | |||||||
| chr7:94409497 | A | T | 2 | a0001c0002t0002g0040 a0001c0002t0002g0103 |
3 | HG02523.hp1 NA18998.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.892-67A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 17/51 | chr7 | 94409497 | |||||||
| chr7:94409622 | C | T | 223 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0022 others(220): Show |
380 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(377): Show |
intron_variant | MODIFIER | c.936+14C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 18/51 | chr7 | 94409622 | |||||||
| chr7:94409654 | G | A | 28 | a0001c0002t0003g0104 a0001c0002t0004g0124 a0001c0006t0001g0015 others(25): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.936+46G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 18/51 | chr7 | 94409654 | |||||||
| chr7:94409720 | C | T | 223 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0022 others(220): Show |
380 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(377): Show |
splice_region_variant&intron_variant | LOW | c.937-3C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 18/51 | chr7 | 94409720 | |||||||
| chr7:94409875 | A | G | 96 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0042 others(93): Show |
160 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.1035+54A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 19/51 | chr7 | 94409875 | |||||||
| chr7:94410098 | C | G | 96 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0042 others(93): Show |
160 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.1036-144C>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 19/51 | chr7 | 94410098 | |||||||
| chr7:94410197 | C | T | 1 | a0001c0022t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1036-45C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 19/51 | chr7 | 94410197 | |||||||
| chr7:94410204 | T | C | 1 | a0001c0008t0001g0197 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1036-38T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 19/51 | chr7 | 94410204 | |||||||
| chr7:94410228 | G | A | 1 | a0001c0006t0001g0232 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1036-14G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 19/51 | chr7 | 94410228 | |||||||
| chr7:94410230 | A | G | 1 | a0002c0004t0002g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1036-12A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 19/51 | chr7 | 94410230 | |||||||
| chr7:94410381 | T | A | 1 | a0001c0024t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1090-39T>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 20/51 | chr7 | 94410381 | |||||||
| chr7:94410581 | C | T | 2 | a0003c0013t0001g0065 a0003c0013t0001g0066 |
2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1197+54C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 21/51 | chr7 | 94410581 | |||||||
| chr7:94410588 | C | T | 222 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0022 others(219): Show |
379 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(376): Show |
intron_variant | MODIFIER | c.1197+61C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 21/51 | chr7 | 94410588 | |||||||
| chr7:94410738 | T | C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1198-151T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 21/51 | chr7 | 94410738 | |||||||
| chr7:94410821 | T | A | 245 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0022 others(242): Show |
414 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(411): Show |
intron_variant | MODIFIER | c.1198-68T>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 21/51 | chr7 | 94410821 | |||||||
| chr7:94410867 | T | C | 3 | a0001c0002t0001g0211 a0001c0014t0002g0210 a0001c0017t0006g0234 |
3 | HG03209.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1198-22T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 21/51 | chr7 | 94410867 | |||||||
| chr7:94410975 | G | A | 40 | a0001c0001t0001g0022 a0001c0001t0001g0029 a0001c0001t0001g0058 others(37): Show |
63 | HG00597.hp1 HG00673.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.1251+33G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 22/51 | chr7 | 94410975 | |||||||
| chr7:94411033 | G | GT | 5 | a0001c0002t0001g0039 a0001c0002t0001g0102 a0001c0002t0003g0031 others(2): Show |
7 | HG00621.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1252-7dupT | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 22/51 | INFO_REALIGN_3_PRIME | chr7 | 94411033 | ||||||
| chr7:94411033 | GT | G | 41 | a0001c0001t0001g0022 a0001c0001t0001g0029 a0001c0001t0001g0058 others(38): Show |
64 | HG00597.hp1 HG00673.hp1 HG00733.hp2 others(61): Show |
splice_region_variant&intron_variant | LOW | c.1252-7delT | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 22/51 | INFO_REALIGN_3_PRIME | chr7 | 94411033 | ||||||
| chr7:94411197 | C | T | 3 | a0001c0002t0001g0211 a0001c0014t0002g0210 a0001c0017t0006g0234 |
3 | HG03209.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1350+43C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 23/51 | chr7 | 94411197 | |||||||
| chr7:94411386 | A | G | 2 | a0003c0013t0001g0065 a0003c0013t0001g0066 |
2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1350+232A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 23/51 | chr7 | 94411386 | |||||||
| chr7:94411389 | G | T | 3 | a0001c0001t0002g0059 a0001c0001t0002g0217 a0001c0001t0002g0235 |
4 | HG01978.hp1 HG02135.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.1350+235G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 23/51 | chr7 | 94411389 | |||||||
| chr7:94411390 | A | AT | 3 | a0001c0001t0002g0059 a0001c0001t0002g0217 a0001c0001t0002g0235 |
4 | HG01978.hp1 HG02135.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.1350+237dupT | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 23/51 | INFO_REALIGN_3_PRIME | chr7 | 94411390 | ||||||
| chr7:94411504 | G | C | 73 | a0001c0002t0001g0001 a0001c0002t0001g0017 a0001c0002t0001g0025 others(70): Show |
139 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1350+350G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 23/51 | chr7 | 94411504 | |||||||
| chr7:94411643 | C | A | 4 | a0002c0004t0001g0075 a0002c0004t0002g0018 a0002c0004t0002g0130 others(1): Show |
7 | HG00544.hp1 HG02083.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.1351-425C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 23/51 | chr7 | 94411643 | |||||||
| chr7:94411648 | A | G | 5 | a0001c0002t0001g0038 a0001c0002t0001g0085 a0001c0002t0001g0086 others(2): Show |
6 | HG00438.hp1 HG00673.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1351-420A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 23/51 | chr7 | 94411648 | |||||||
| chr7:94411651 | G | A | 213 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0022 others(210): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(367): Show |
intron_variant | MODIFIER | c.1351-417G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 23/51 | chr7 | 94411651 | |||||||
| chr7:94411687 | T | C | 42 | a0001c0002t0001g0001 a0001c0002t0001g0017 a0001c0002t0001g0025 others(39): Show |
82 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1351-381T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 23/51 | chr7 | 94411687 | |||||||
| chr7:94411812 | T | G | 1 | a0002c0004t0002g0050 | 2 | HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1351-256T>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 23/51 | chr7 | 94411812 | |||||||
| chr7:94411864 | A | T | 1 | a0003c0033t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1351-204A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 23/51 | chr7 | 94411864 | |||||||
| chr7:94411941 | A | C | 1 | a0001c0003t0001g0228 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1351-127A>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 23/51 | chr7 | 94411941 | |||||||
| chr7:94412281 | A | G | 1 | a0002c0004t0003g0132 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1404+160A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 24/51 | chr7 | 94412281 | |||||||
| chr7:94412309 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0169 a0010c0027t0001g0052 |
3 | HG02451.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1404+188G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 24/51 | chr7 | 94412309 | |||||||
| chr7:94412568 | A | G | 1 | a0003c0033t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1405-16A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 24/51 | chr7 | 94412568 | |||||||
| chr7:94413007 | T | C | 1 | a0012c0036t0001g0180 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1504-76T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 25/51 | chr7 | 94413007 | |||||||
| chr7:94413079 | C | A | 1 | a0001c0001t0001g0110 | 1 | NA18522.hp1 | splice_region_variant&intron_variant | LOW | c.1504-4C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 25/51 | chr7 | 94413079 | |||||||
| chr7:94413294 | C | T | 2 | a0001c0002t0001g0108 a0001c0002t0006g0084 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1557+158C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 26/51 | chr7 | 94413294 | |||||||
| chr7:94413502 | T | C | 79 | a0001c0002t0003g0104 a0001c0002t0004g0124 a0001c0003t0001g0003 others(76): Show |
137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1558-188T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 26/51 | chr7 | 94413502 | |||||||
| chr7:94413555 | C | T | 1 | a0001c0006t0002g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1558-135C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 26/51 | chr7 | 94413555 | |||||||
| chr7:94413587 | A | T | 1 | a0001c0002t0001g0099 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1558-103A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 26/51 | chr7 | 94413587 | |||||||
| chr7:94413618 | C | T | 2 | a0001c0007t0001g0021 a0001c0009t0001g0162 |
5 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558-72C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 26/51 | chr7 | 94413618 | |||||||
| chr7:94413848 | T | C | 3 | a0001c0006t0001g0232 a0001c0009t0001g0073 a0001c0009t0001g0137 |
3 | HG02615.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1612-46T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 27/51 | chr7 | 94413848 | |||||||
| chr7:94413962 | A | G | 62 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0067 others(59): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1665+15A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 28/51 | chr7 | 94413962 | |||||||
| chr7:94414013 | C | T | 1 | a0001c0015t0005g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1665+66C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 28/51 | chr7 | 94414013 | |||||||
| chr7:94414085 | A | G | 1 | a0001c0009t0003g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1666-137A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 28/51 | chr7 | 94414085 | |||||||
| chr7:94414181 | G | A | 41 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0029 others(38): Show |
67 | HG00597.hp1 HG00673.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.1666-41G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 28/51 | chr7 | 94414181 | |||||||
| chr7:94414382 | T | C | 1 | a0001c0001t0005g0082 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1719+107T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 29/51 | chr7 | 94414382 | |||||||
| chr7:94414559 | C | T | 11 | a0002c0004t0001g0075 a0002c0004t0001g0145 a0002c0004t0002g0012 others(8): Show |
21 | HG00544.hp1 HG01081.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.1719+284C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 29/51 | chr7 | 94414559 | |||||||
| chr7:94414716 | C | A | 2 | a0001c0007t0001g0021 a0001c0009t0001g0162 |
5 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1719+441C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 29/51 | chr7 | 94414716 | |||||||
| chr7:94414776 | C | G | 1 | a0001c0001t0002g0178 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1720-450C>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 29/51 | chr7 | 94414776 | |||||||
| chr7:94414881 | C | T | 1 | a0001c0007t0001g0076 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1720-345C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 29/51 | chr7 | 94414881 | |||||||
| chr7:94414882 | G | A | 2 | a0003c0013t0001g0065 a0003c0013t0001g0066 |
2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1720-344G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 29/51 | chr7 | 94414882 | |||||||
| chr7:94414910 | T | C | 240 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0022 others(237): Show |
407 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(404): Show |
intron_variant | MODIFIER | c.1720-316T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 29/51 | chr7 | 94414910 | |||||||
| chr7:94414923 | T | G | 1 | a0001c0007t0001g0076 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1720-303T>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 29/51 | chr7 | 94414923 | |||||||
| chr7:94415021 | A | T | 2 | a0001c0003t0002g0188 a0001c0003t0003g0055 |
3 | NA18980.hp2 NA19057.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1720-205A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 29/51 | chr7 | 94415021 | |||||||
| chr7:94415090 | T | C | 1 | a0001c0022t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1720-136T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 29/51 | chr7 | 94415090 | |||||||
| chr7:94415355 | C | T | 5 | a0001c0014t0002g0210 a0001c0017t0006g0234 a0001c0020t0003g0242 others(2): Show |
5 | HG03225.hp1 HG03225.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1764+85C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 30/51 | chr7 | 94415355 | |||||||
| chr7:94415356 | C | T | 5 | a0001c0001t0004g0172 a0001c0009t0003g0241 a0001c0009t0003g0243 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1764+86C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 30/51 | chr7 | 94415356 | |||||||
| chr7:94415371 | T | C | 1 | a0001c0007t0005g0056 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1764+101T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 30/51 | chr7 | 94415371 | |||||||
| chr7:94415411 | T | C | 3 | a0001c0005t0001g0041 a0001c0005t0001g0116 a0001c0005t0003g0115 |
4 | HG03491.hp1 HG03492.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1764+141T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 30/51 | chr7 | 94415411 | |||||||
| chr7:94415491 | C | A | 61 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0067 others(58): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1764+221C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 30/51 | chr7 | 94415491 | |||||||
| chr7:94415762 | G | A | 54 | a0001c0003t0001g0003 a0001c0003t0001g0006 a0001c0003t0001g0013 others(51): Show |
96 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1764+492G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 30/51 | chr7 | 94415762 | |||||||
| chr7:94415772 | AGAACCAA others(18): Show |
A | 1 | a0001c0001t0002g0203 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1764+506_1764+530d others(27): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 30/51 | INFO_REALIGN_3_PRIME | chr7 | 94415772 | ||||||
| chr7:94415842 | T | C | 40 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0029 others(37): Show |
66 | HG00597.hp1 HG00673.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.1765-563T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 30/51 | chr7 | 94415842 | |||||||
| chr7:94415854 | C | T | 62 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0067 others(59): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1765-551C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 30/51 | chr7 | 94415854 | |||||||
| chr7:94415923 | C | T | 1 | a0001c0022t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1765-482C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 30/51 | chr7 | 94415923 | |||||||
| chr7:94416257 | G | A | 3 | a0001c0006t0001g0232 a0001c0009t0001g0073 a0001c0009t0001g0137 |
3 | HG02615.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1765-148G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 30/51 | chr7 | 94416257 | |||||||
| chr7:94416264 | G | A | 147 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0023 others(144): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.1765-141G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 30/51 | chr7 | 94416264 | |||||||
| chr7:94416648 | G | C | 1 | a0001c0006t0001g0048 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1863+145G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 31/51 | chr7 | 94416648 | |||||||
| chr7:94416766 | C | T | 4 | a0001c0003t0001g0054 a0001c0003t0001g0181 a0001c0003t0001g0226 others(1): Show |
5 | HG01934.hp2 HG02129.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.1863+263C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 31/51 | chr7 | 94416766 | |||||||
| chr7:94416887 | C | A | 40 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0029 others(37): Show |
66 | HG00597.hp1 HG00673.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.1863+384C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 31/51 | chr7 | 94416887 | |||||||
| chr7:94416993 | T | A | 1 | a0003c0033t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1863+490T>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 31/51 | chr7 | 94416993 | |||||||
| chr7:94417053 | A | T | 1 | a0001c0002t0001g0098 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1863+550A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 31/51 | chr7 | 94417053 | |||||||
| chr7:94417063 | A | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0169 others(2): Show |
8 | HG01891.hp1 HG02451.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1863+560A>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 31/51 | chr7 | 94417063 | |||||||
| chr7:94417156 | A | G | 59 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0067 others(56): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1864-568A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 31/51 | chr7 | 94417156 | |||||||
| chr7:94417195 | G | A | 1 | a0001c0014t0001g0109 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1864-529G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 31/51 | chr7 | 94417195 | |||||||
| chr7:94417229 | G | T | 101 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0023 others(98): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.1864-495G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 31/51 | chr7 | 94417229 | |||||||
| chr7:94417364 | C | T | 35 | a0001c0001t0001g0022 a0001c0001t0001g0029 a0001c0001t0001g0058 others(32): Show |
58 | HG00597.hp1 HG00673.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1864-360C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 31/51 | chr7 | 94417364 | |||||||
| chr7:94417540 | C | A | 3 | a0001c0006t0001g0232 a0001c0009t0001g0073 a0001c0009t0001g0137 |
3 | HG02615.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1864-184C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 31/51 | chr7 | 94417540 | |||||||
| chr7:94417545 | C | T | 1 | a0001c0007t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1864-179C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 31/51 | chr7 | 94417545 | |||||||
| chr7:94417605 | G | A | 1 | a0001c0001t0002g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1864-119G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 31/51 | chr7 | 94417605 | |||||||
| chr7:94417650 | GA | G | 5 | a0001c0014t0002g0210 a0001c0017t0006g0234 a0001c0020t0003g0242 others(2): Show |
5 | HG03225.hp1 HG03225.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1864-72delA | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 31/51 | INFO_REALIGN_3_PRIME | chr7 | 94417650 | ||||||
| chr7:94417849 | T | C | 1 | a0003c0033t0001g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1971+18T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 32/51 | chr7 | 94417849 | |||||||
| chr7:94417877 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1971+46G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 32/51 | chr7 | 94417877 | |||||||
| chr7:94417954 | C | A | 54 | a0001c0003t0001g0003 a0001c0003t0001g0006 a0001c0003t0001g0013 others(51): Show |
96 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1971+123C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 32/51 | chr7 | 94417954 | |||||||
| chr7:94417981 | A | G | 1 | a0002c0004t0002g0130 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1971+150A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 32/51 | chr7 | 94417981 | |||||||
| chr7:94418102 | T | A | 1 | a0002c0004t0003g0147 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1971+271T>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 32/51 | chr7 | 94418102 | |||||||
| chr7:94418165 | C | A | 1 | a0001c0002t0001g0211 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1971+334C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 32/51 | chr7 | 94418165 | |||||||
| chr7:94418166 | G | A | 1 | a0001c0002t0001g0090 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1972-333G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 32/51 | chr7 | 94418166 | |||||||
| chr7:94418349 | C | T | 1 | a0001c0001t0005g0082 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1972-150C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 32/51 | chr7 | 94418349 | |||||||
| chr7:94418365 | C | T | 56 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0110 others(53): Show |
100 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1972-134C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 32/51 | chr7 | 94418365 | |||||||
| chr7:94418480 | T | C | 1 | a0001c0003t0001g0191 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1972-19T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 32/51 | chr7 | 94418480 | |||||||
| chr7:94418582 | C | T | 1 | a0002c0004t0002g0144 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2025+30C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94418582 | |||||||
| chr7:94418591 | AT | A | 61 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0067 others(58): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2025+49delT | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | INFO_REALIGN_3_PRIME | chr7 | 94418591 | ||||||
| chr7:94418601 | TA | T | 75 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0110 others(72): Show |
122 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.2025+50delA | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94418601 | |||||||
| chr7:94418602 | A | T | 1 | a0001c0003t0004g0221 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2025+50A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94418602 | |||||||
| chr7:94418643 | CTT | C | 3 | a0001c0006t0001g0232 a0001c0009t0001g0073 a0001c0009t0001g0137 |
3 | HG02615.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2025+93_2025+94del others(2): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | INFO_REALIGN_3_PRIME | chr7 | 94418643 | ||||||
| chr7:94418816 | C | T | 5 | a0001c0014t0002g0210 a0001c0017t0006g0234 a0001c0020t0003g0242 others(2): Show |
5 | HG03225.hp1 HG03225.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2025+264C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94418816 | |||||||
| chr7:94418853 | C | T | 61 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0067 others(58): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2025+301C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94418853 | |||||||
| chr7:94418911 | A | T | 1 | a0001c0001t0002g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2025+359A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94418911 | |||||||
| chr7:94418914 | C | T | 1 | a0001c0003t0001g0225 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2025+362C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94418914 | |||||||
| chr7:94418917 | G | A | 61 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0067 others(58): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.2025+365G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94418917 | |||||||
| chr7:94418936 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG00140.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2025+384T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94418936 | |||||||
| chr7:94419170 | G | A | 85 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0029 others(82): Show |
151 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.2026-328G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94419170 | |||||||
| chr7:94419180 | C | G | 7 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0169 others(4): Show |
11 | HG01891.hp1 HG02451.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.2026-318C>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94419180 | |||||||
| chr7:94419222 | T | G | 10 | a0001c0002t0003g0104 a0001c0002t0004g0124 a0001c0006t0001g0024 others(7): Show |
16 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2026-276T>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94419222 | |||||||
| chr7:94419233 | G | A | 40 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0029 others(37): Show |
66 | HG00597.hp1 HG00673.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.2026-265G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94419233 | |||||||
| chr7:94419278 | C | A | 1 | a0002c0004t0001g0145 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2026-220C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94419278 | |||||||
| chr7:94419315 | TGA | T | 53 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0067 others(50): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.2026-179_2026-178d others(4): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | INFO_REALIGN_3_PRIME | chr7 | 94419315 | ||||||
| chr7:94419367 | C | T | 2 | a0001c0001t0002g0146 a0001c0022t0001g0161 |
2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2026-131C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | chr7 | 94419367 | |||||||
| chr7:94419464 | TTA | T | 40 | a0001c0003t0001g0003 a0001c0003t0001g0006 a0001c0003t0001g0013 others(37): Show |
77 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.2026-32_2026-31del others(2): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 33/51 | INFO_REALIGN_3_PRIME | chr7 | 94419464 | ||||||
| chr7:94419573 | G | C | 2 | a0001c0001t0002g0146 a0001c0022t0001g0161 |
2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2079+22G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 34/51 | chr7 | 94419573 | |||||||
| chr7:94419661 | A | G | 1 | a0001c0002t0001g0097 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2079+110A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 34/51 | chr7 | 94419661 | |||||||
| chr7:94419904 | A | G | 1 | a0001c0002t0001g0025 | 3 | HG02080.hp1 NA18952.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.2080-329A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 34/51 | chr7 | 94419904 | |||||||
| chr7:94419971 | A | C | 3 | a0001c0002t0001g0108 a0001c0002t0001g0173 a0001c0002t0006g0084 |
3 | HG01891.hp2 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2080-262A>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 34/51 | chr7 | 94419971 | |||||||
| chr7:94420037 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0240 |
5 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2080-196C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 34/51 | chr7 | 94420037 | |||||||
| chr7:94420041 | T | C | 3 | a0001c0001t0002g0146 a0001c0022t0001g0161 a0001c0024t0001g0133 |
3 | HG02717.hp1 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2080-192T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 34/51 | chr7 | 94420041 | |||||||
| chr7:94420044 | T | C | 146 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0023 others(143): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.2080-189T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 34/51 | chr7 | 94420044 | |||||||
| chr7:94420110 | C | T | 5 | a0001c0014t0002g0210 a0001c0017t0006g0234 a0001c0020t0003g0242 others(2): Show |
5 | HG03225.hp1 HG03225.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2080-123C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 34/51 | chr7 | 94420110 | |||||||
| chr7:94420157 | C | G | 1 | a0001c0001t0003g0122 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2080-76C>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 34/51 | chr7 | 94420157 | |||||||
| chr7:94420167 | T | C | 1 | a0007c0031t0001g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2080-66T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 34/51 | chr7 | 94420167 | |||||||
| chr7:94420172 | C | T | 3 | a0001c0014t0002g0210 a0001c0017t0006g0234 a0001c0020t0003g0242 |
3 | HG03225.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2080-61C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 34/51 | chr7 | 94420172 | |||||||
| chr7:94420185 | G | C | 1 | a0001c0002t0001g0087 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2080-48G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 34/51 | chr7 | 94420185 | |||||||
| chr7:94420695 | C | T | 1 | a0001c0022t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2295+47C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 37/51 | chr7 | 94420695 | |||||||
| chr7:94420769 | C | T | 1 | a0001c0003t0001g0030 | 3 | NA18971.hp2 NA18975.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.2295+121C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 37/51 | chr7 | 94420769 | |||||||
| chr7:94421078 | G | C | 3 | a0001c0002t0001g0108 a0001c0002t0001g0173 a0001c0002t0006g0084 |
3 | HG01891.hp2 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2349+16G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 38/51 | chr7 | 94421078 | |||||||
| chr7:94421102 | C | G | 3 | a0001c0002t0001g0108 a0001c0002t0001g0173 a0001c0002t0006g0084 |
3 | HG01891.hp2 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2349+40C>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 38/51 | chr7 | 94421102 | |||||||
| chr7:94421110 | A | G | 1 | a0001c0001t0002g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2349+48A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 38/51 | chr7 | 94421110 | |||||||
| chr7:94421296 | T | G | 32 | a0001c0001t0001g0159 a0001c0001t0004g0126 a0001c0002t0003g0104 others(29): Show |
56 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.2349+234T>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 38/51 | chr7 | 94421296 | |||||||
| chr7:94421346 | C | G | 1 | a0001c0022t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2349+284C>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 38/51 | chr7 | 94421346 | |||||||
| chr7:94421449 | C | T | 1 | a0001c0003t0002g0008 | 6 | HG00621.hp2 NA18944.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.2349+387C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 38/51 | chr7 | 94421449 | |||||||
| chr7:94421642 | A | G | 1 | a0001c0005t0002g0121 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2350-257A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 38/51 | chr7 | 94421642 | |||||||
| chr7:94421659 | C | G | 3 | a0001c0002t0001g0038 a0001c0002t0001g0086 a0001c0002t0001g0101 |
4 | HG00673.hp2 NA18975.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.2350-240C>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 38/51 | chr7 | 94421659 | |||||||
| chr7:94421772 | CCTACCTC others(31): Show |
C | 48 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0117 others(45): Show |
93 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.2350-124_2350-87de others(39): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 38/51 | INFO_REALIGN_3_PRIME | chr7 | 94421772 | ||||||
| chr7:94422098 | A | G | 1 | a0005c0030t0001g0096 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2403+146A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 39/51 | chr7 | 94422098 | |||||||
| chr7:94422138 | T | C | 2 | a0001c0002t0002g0151 a0001c0002t0003g0011 |
6 | HG00642.hp1 HG01069.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.2403+186T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 39/51 | chr7 | 94422138 | |||||||
| chr7:94422195 | GA | G | 186 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0022 others(183): Show |
319 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(316): Show |
intron_variant | MODIFIER | c.2403+255delA | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 39/51 | INFO_REALIGN_3_PRIME | chr7 | 94422195 | ||||||
| chr7:94422195 | GAA | G | 10 | a0001c0001t0002g0146 a0001c0008t0001g0005 a0001c0008t0001g0197 others(7): Show |
17 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2403+254_2403+255d others(4): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 39/51 | INFO_REALIGN_3_PRIME | chr7 | 94422195 | ||||||
| chr7:94422233 | A | T | 1 | a0014c0028t0002g0207 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2403+281A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 39/51 | chr7 | 94422233 | |||||||
| chr7:94422483 | C | A | 24 | a0001c0001t0004g0126 a0001c0002t0003g0104 a0001c0002t0004g0124 others(21): Show |
41 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.2404-474C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 39/51 | chr7 | 94422483 | |||||||
| chr7:94422498 | G | A | 1 | a0001c0002t0001g0090 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2404-459G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 39/51 | chr7 | 94422498 | |||||||
| chr7:94422572 | TA | T | 104 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0023 others(101): Show |
187 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.2404-370delA | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 39/51 | INFO_REALIGN_3_PRIME | chr7 | 94422572 | ||||||
| chr7:94422604 | G | A | 74 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0051 others(71): Show |
119 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.2404-353G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 39/51 | chr7 | 94422604 | |||||||
| chr7:94422639 | A | G | 1 | a0001c0022t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2404-318A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 39/51 | chr7 | 94422639 | |||||||
| chr7:94422721 | A | T | 1 | a0001c0029t0007g0168 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2404-236A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 39/51 | chr7 | 94422721 | |||||||
| chr7:94422843 | G | T | 1 | a0001c0003t0001g0227 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2404-114G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 39/51 | chr7 | 94422843 | |||||||
| chr7:94423183 | A | G | 48 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0117 others(45): Show |
93 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.2565+65A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | chr7 | 94423183 | |||||||
| chr7:94423282 | G | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 |
3 | HG02486.hp2 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2565+164G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | chr7 | 94423282 | |||||||
| chr7:94423291 | A | G | 30 | a0001c0005t0001g0007 a0001c0005t0001g0010 a0001c0005t0001g0041 others(27): Show |
45 | HG00558.hp1 HG00621.hp1 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.2565+173A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | chr7 | 94423291 | |||||||
| chr7:94423319 | C | A | 1 | a0007c0031t0001g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2565+201C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | chr7 | 94423319 | |||||||
| chr7:94423343 | A | T | 3 | a0001c0006t0001g0232 a0001c0009t0001g0073 a0001c0009t0001g0137 |
3 | HG02615.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2565+225A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | chr7 | 94423343 | |||||||
| chr7:94423351 | G | A | 48 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0117 others(45): Show |
93 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.2565+233G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | chr7 | 94423351 | |||||||
| chr7:94423364 | T | C | 2 | a0002c0004t0002g0141 a0002c0004t0002g0154 |
2 | HG00642.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2565+246T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | chr7 | 94423364 | |||||||
| chr7:94423461 | A | C | 1 | a0007c0031t0001g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2565+343A>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | chr7 | 94423461 | |||||||
| chr7:94423569 | C | CTTTTTGT others(6): Show |
1 | a0001c0009t0001g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2565+469_2565+481d others(15): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | INFO_REALIGN_3_PRIME | chr7 | 94423569 | ||||||
| chr7:94423569 | C | CTTTTTGT others(12): Show |
1 | a0001c0009t0001g0137 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2565+470_2565+488d others(21): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | INFO_REALIGN_3_PRIME | chr7 | 94423569 | ||||||
| chr7:94423569 | CTTTTTGT others(6): Show |
C | 1 | a0012c0036t0001g0180 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2565+469_2565+481d others(15): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | INFO_REALIGN_3_PRIME | chr7 | 94423569 | ||||||
| chr7:94423615 | G | A | 4 | a0001c0006t0001g0232 a0001c0009t0001g0073 a0001c0009t0001g0137 others(1): Show |
4 | HG02615.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2565+497G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | chr7 | 94423615 | |||||||
| chr7:94423693 | T | C | 200 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0023 others(197): Show |
347 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(344): Show |
intron_variant | MODIFIER | c.2565+575T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | chr7 | 94423693 | |||||||
| chr7:94423788 | T | A | 1 | a0001c0002t0001g0211 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2566-548T>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | chr7 | 94423788 | |||||||
| chr7:94424253 | A | G | 3 | a0001c0002t0001g0108 a0001c0002t0001g0173 a0001c0002t0006g0084 |
3 | HG01891.hp2 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2566-83A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 40/51 | chr7 | 94424253 | |||||||
| chr7:94424570 | T | C | 1 | a0001c0009t0001g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2673+127T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 41/51 | chr7 | 94424570 | |||||||
| chr7:94424688 | T | C | 200 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0023 others(197): Show |
347 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(344): Show |
intron_variant | MODIFIER | c.2673+245T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 41/51 | chr7 | 94424688 | |||||||
| chr7:94424707 | G | A | 1 | a0001c0006t0002g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2673+264G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 41/51 | chr7 | 94424707 | |||||||
| chr7:94424737 | A | G | 2 | a0001c0002t0001g0097 a0013c0032t0001g0095 |
2 | NA18951.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2673+294A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 41/51 | chr7 | 94424737 | |||||||
| chr7:94424803 | G | T | 3 | a0001c0006t0001g0232 a0001c0009t0001g0073 a0001c0009t0001g0137 |
3 | HG02615.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2674-314G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 41/51 | chr7 | 94424803 | |||||||
| chr7:94424840 | A | G | 1 | a0002c0004t0002g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2674-277A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 41/51 | chr7 | 94424840 | |||||||
| chr7:94424882 | C | T | 28 | a0001c0005t0001g0007 a0001c0005t0001g0010 a0001c0005t0001g0041 others(25): Show |
43 | HG00558.hp1 HG00621.hp1 HG01175.hp1 others(40): Show |
intron_variant | MODIFIER | c.2674-235C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 41/51 | chr7 | 94424882 | |||||||
| chr7:94424911 | C | T | 49 | a0001c0001t0001g0042 a0001c0003t0001g0003 a0001c0003t0001g0006 others(46): Show |
84 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.2674-206C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 41/51 | chr7 | 94424911 | |||||||
| chr7:94425869 | A | T | 1 | a0001c0009t0003g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2943+12A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 44/51 | chr7 | 94425869 | |||||||
| chr7:94425908 | T | C | 1 | a0001c0002t0003g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2943+51T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 44/51 | chr7 | 94425908 | |||||||
| chr7:94425930 | G | A | 1 | a0001c0005t0001g0119 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2944-68G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 44/51 | chr7 | 94425930 | |||||||
| chr7:94426158 | T | A | 10 | a0001c0001t0002g0146 a0001c0006t0001g0232 a0001c0008t0001g0005 others(7): Show |
17 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2997+107T>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 45/51 | chr7 | 94426158 | |||||||
| chr7:94426573 | G | A | 25 | a0001c0005t0001g0007 a0001c0005t0001g0010 a0001c0005t0001g0041 others(22): Show |
40 | HG00558.hp1 HG00621.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.3105+43G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 46/51 | chr7 | 94426573 | |||||||
| chr7:94426605 | A | T | 1 | a0001c0002t0002g0094 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3105+75A>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 46/51 | chr7 | 94426605 | |||||||
| chr7:94426621 | T | C | 36 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0052 others(33): Show |
64 | HG00597.hp1 HG00673.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.3105+91T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 46/51 | chr7 | 94426621 | |||||||
| chr7:94426675 | G | T | 1 | a0002c0004t0001g0075 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3105+145G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 46/51 | chr7 | 94426675 | |||||||
| chr7:94426694 | A | G | 117 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0023 others(114): Show |
205 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.3105+164A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 46/51 | chr7 | 94426694 | |||||||
| chr7:94426732 | G | T | 199 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0023 others(196): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.3105+202G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 46/51 | chr7 | 94426732 | |||||||
| chr7:94426787 | A | G | 30 | a0001c0005t0001g0007 a0001c0005t0001g0010 a0001c0005t0001g0041 others(27): Show |
45 | HG00558.hp1 HG00621.hp1 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.3106-221A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 46/51 | chr7 | 94426787 | |||||||
| chr7:94426833 | A | G | 7 | a0001c0001t0002g0146 a0001c0008t0001g0005 a0001c0008t0001g0197 others(4): Show |
14 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.3106-175A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 46/51 | chr7 | 94426833 | |||||||
| chr7:94426904 | G | A | 30 | a0001c0005t0001g0007 a0001c0005t0001g0010 a0001c0005t0001g0041 others(27): Show |
45 | HG00558.hp1 HG00621.hp1 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.3106-104G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 46/51 | chr7 | 94426904 | |||||||
| chr7:94426932 | C | G | 134 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0022 others(131): Show |
232 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.3106-76C>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 46/51 | chr7 | 94426932 | |||||||
| chr7:94426939 | GAA | G | 178 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0022 others(175): Show |
311 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.3106-56_3106-55del others(2): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 46/51 | INFO_REALIGN_3_PRIME | chr7 | 94426939 | ||||||
| chr7:94427329 | C | T | 1 | a0001c0005t0001g0125 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3267+34C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 48/51 | chr7 | 94427329 | |||||||
| chr7:94427389 | G | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0110 others(10): Show |
22 | HG00621.hp2 HG02145.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.3267+94G>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 48/51 | chr7 | 94427389 | |||||||
| chr7:94427462 | C | T | 1 | a0001c0035t0001g0089 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3268-165C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 48/51 | chr7 | 94427462 | |||||||
| chr7:94427544 | G | A | 1 | a0002c0004t0002g0144 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3268-83G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 48/51 | chr7 | 94427544 | |||||||
| chr7:94427962 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3526+77G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 49/51 | chr7 | 94427962 | |||||||
| chr7:94428098 | C | A | 1 | a0004c0012t0001g0222 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3527-195C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 49/51 | chr7 | 94428098 | |||||||
| chr7:94428106 | A | C | 29 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0169 others(26): Show |
47 | HG00280.hp2 HG00438.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.3527-187A>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 49/51 | chr7 | 94428106 | |||||||
| chr7:94428266 | A | G | 1 | a0001c0006t0001g0048 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3527-27A>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 49/51 | chr7 | 94428266 | |||||||
| chr7:94428525 | T | A | 1 | a0001c0006t0002g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3711+48T>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 50/51 | chr7 | 94428525 | |||||||
| chr7:94428816 | C | A | 5 | a0001c0006t0001g0232 a0001c0009t0001g0137 a0003c0013t0001g0065 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.3711+339C>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 50/51 | chr7 | 94428816 | |||||||
| chr7:94428886 | T | C | 65 | a0001c0001t0001g0042 a0001c0002t0001g0102 a0001c0002t0002g0093 others(62): Show |
113 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.3712-302T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 50/51 | chr7 | 94428886 | |||||||
| chr7:94428889 | GA | G | 12 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0110 others(9): Show |
21 | HG00621.hp2 HG02145.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.3712-297delA | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 50/51 | INFO_REALIGN_3_PRIME | chr7 | 94428889 | ||||||
| chr7:94429003 | A | C | 1 | a0001c0003t0001g0225 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3712-185A>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 50/51 | chr7 | 94429003 | |||||||
| chr7:94429083 | T | C | 146 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0042 others(143): Show |
231 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(228): Show |
intron_variant | MODIFIER | c.3712-105T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 50/51 | chr7 | 94429083 | |||||||
| chr7:94429086 | T | C | 9 | a0001c0001t0001g0112 a0001c0002t0001g0211 a0001c0007t0001g0174 others(6): Show |
16 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3712-102T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 50/51 | chr7 | 94429086 | |||||||
| chr7:94429106 | T | TTTC | 8 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0169 others(5): Show |
11 | HG00738.hp1 HG01891.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.3712-81_3712-80ins others(3): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 50/51 | INFO_REALIGN_3_PRIME | chr7 | 94429106 | ||||||
| chr7:94429107 | T | TTC | 154 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0051 others(151): Show |
257 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(254): Show |
intron_variant | MODIFIER | c.3712-81_3712-80ins others(2): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 50/51 | chr7 | 94429107 | |||||||
| chr7:94429108 | C | T | 162 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0042 others(159): Show |
268 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(265): Show |
intron_variant | MODIFIER | c.3712-80C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 50/51 | chr7 | 94429108 | |||||||
| chr7:94429117 | T | C | 1 | a0002c0004t0002g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3712-71T>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 50/51 | chr7 | 94429117 | |||||||
| chr7:94429175 | C | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0111 others(10): Show |
22 | HG00621.hp2 HG01243.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.3712-13C>T | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 50/51 | chr7 | 94429175 | |||||||
| chr7:94429506 | G | C | 2 | a0001c0002t0001g0036 a0001c0006t0004g0078 |
3 | NA18949.hp1 NA18984.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.3954+76G>C | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/51 | chr7 | 94429506 | |||||||
| chr7:94429545 | GAACT | G | 10 | a0001c0001t0001g0029 a0001c0001t0001g0159 a0001c0001t0001g0206 others(7): Show |
11 | HG00741.hp2 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3954+120_3954+123d others(6): Show |
COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/51 | INFO_REALIGN_3_PRIME | chr7 | 94429545 | ||||||
| chr7:94429663 | G | A | 1 | a0001c0022t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3954+233G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/51 | chr7 | 94429663 | |||||||
| chr7:94429854 | TA | T | 2 | a0001c0005t0001g0041 a0001c0005t0001g0116 |
3 | HG03491.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3955-392delA | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/51 | chr7 | 94429854 | |||||||
| chr7:94429924 | G | A | 13 | a0001c0001t0001g0117 a0001c0001t0001g0171 a0001c0002t0001g0037 others(10): Show |
19 | HG00621.hp1 HG01175.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.3955-323G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/51 | chr7 | 94429924 | |||||||
| chr7:94430005 | G | A | 53 | a0001c0001t0002g0002 a0001c0001t0002g0053 a0001c0001t0002g0059 others(50): Show |
89 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.3955-242G>A | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/51 | chr7 | 94430005 | |||||||
| chr7:94430032 | T | G | 57 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0062 others(54): Show |
105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.3955-215T>G | COL1A2 | ENSG00000164692.19 | transcript | ENST00000297268.11 | protein_coding | 51/51 | chr7 | 94430032 |