Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 129804 |
| ensemblid | ENSG00000144152.13 |
| hgncid | 26740 |
| symbol | FBLN7 |
| name | fibulin 7 |
| refseq_nuc | NM_153214.3 |
| refseq_prot | NP_694946.2 |
| ensembl_nuc | ENST00000331203.7 |
| ensembl_prot | ENSP00000331411.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 112138385 |
| end | 112188218 |
| strand | + |
| ver | v1.2 |
| region | chr2:112138385-112188218 |
| region5000 | chr2:112133385-112193218 |
| regionname0 | FBLN7_chr2_112138385_112188218 |
| regionname5000 | FBLN7_chr2_112133385_112193218 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 439 | 329 | 82 | 67 | 125 | 17 | 36 | 91 | FBLN7_chr2_112133385_112193218 | FBLN7 | MVPSS others(434): Show |
chr2 | 112133385 | 112193218 |
| a0002 | 0/0 | 439 | 6 | 5 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | MVPSS others(434): Show |
chr2 | 112133385 | 112193218 |
| a0003 | 0/0 | 438 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | MVPSS others(433): Show |
chr2 | 112133385 | 112193218 |
| a0004 | 0/0 | 439 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | MVPSS others(434): Show |
chr2 | 112133385 | 112193218 |
| a0005 | 0/0 | 439 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | MVPSS others(434): Show |
chr2 | 112133385 | 112193218 |
| a0006 | 0/0 | 439 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | MVPSS others(434): Show |
chr2 | 112133385 | 112193218 |
| a0007 | 0/0 | 439 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | MVPSS others(434): Show |
chr2 | 112133385 | 112193218 |
| a0008 | 0/0 | 439 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | MVPSS others(434): Show |
chr2 | 112133385 | 112193218 |
| a0009 | 0/0 | 439 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | MVPSS others(434): Show |
chr2 | 112133385 | 112193218 |
| a0010 | 0/0 | 439 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | MVPSS others(434): Show |
chr2 | 112133385 | 112193218 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1317 | 325 | 81 | 67 | 125 | 17 | 33 | FBLN7_chr2_112133385_112193218 | FBLN7 | ATGGT others(1312): Show |
chr2 | 112133385 | 112193218 | ||
| a0001c0005 | 0/0 | 1317 | 2 | 0 | 0 | 0 | 0 | 2 | FBLN7_chr2_112133385_112193218 | FBLN7 | ATGGT others(1312): Show |
chr2 | 112133385 | 112193218 | ||
| a0001c0007 | 0/0 | 1317 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | ATGGT others(1312): Show |
chr2 | 112133385 | 112193218 | ||
| a0001c0012 | 0/0 | 1317 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | ATGGT others(1312): Show |
chr2 | 112133385 | 112193218 | ||
| a0002c0002 | 0/0 | 1317 | 6 | 5 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | ATGGT others(1312): Show |
chr2 | 112133385 | 112193218 | ||
| a0003c0003 | 0/0 | 1314 | 3 | 3 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | ATGGT others(1309): Show |
chr2 | 112133385 | 112193218 | ||
| a0004c0004 | 0/0 | 1317 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | ATGGT others(1312): Show |
chr2 | 112133385 | 112193218 | ||
| a0005c0011 | 0/0 | 1317 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | ATGGT others(1312): Show |
chr2 | 112133385 | 112193218 | ||
| a0006c0008 | 0/0 | 1317 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | ATGGT others(1312): Show |
chr2 | 112133385 | 112193218 | ||
| a0007c0009 | 0/0 | 1317 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | ATGGT others(1312): Show |
chr2 | 112133385 | 112193218 | ||
| a0008c0010 | 0/0 | 1317 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | ATGGT others(1312): Show |
chr2 | 112133385 | 112193218 | ||
| a0009c0006 | 0/0 | 1317 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | ATGGT others(1312): Show |
chr2 | 112133385 | 112193218 | ||
| a0010c0013 | 0/0 | 1317 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | ATGGT others(1312): Show |
chr2 | 112133385 | 112193218 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2303 | 256 | 48 | 57 | 117 | 10 | 23 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0001c0001t0002 | 0/0 | 2303 | 21 | 8 | 4 | 2 | 4 | 3 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0001c0001t0003 | 1/0 | 2303 | 21 | 16 | 1 | 0 | 0 | 3 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0001c0001t0004 | 0/0 | 2303 | 9 | 0 | 3 | 5 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0001c0001t0005 | 0/0 | 2302 | 6 | 5 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2297): Show |
chr2 | 112133385 | 112193218 |
| a0001c0001t0006 | 0/0 | 2303 | 6 | 0 | 1 | 0 | 2 | 3 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0001c0001t0008 | 0/0 | 2303 | 2 | 2 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0001c0001t0010 | 0/0 | 2303 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0001c0001t0011 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0001c0001t0012 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0001c0001t0013 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0001c0005t0007 | 0/0 | 2303 | 2 | 0 | 0 | 0 | 0 | 2 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0001c0007t0001 | 0/0 | 2303 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0001c0012t0001 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0002c0002t0001 | 0/0 | 2303 | 2 | 2 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0002c0002t0002 | 0/0 | 2303 | 2 | 2 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0002c0002t0003 | 0/0 | 2303 | 2 | 1 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0003c0003t0001 | 0/0 | 2300 | 3 | 3 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2295): Show |
chr2 | 112133385 | 112193218 |
| a0004c0004t0002 | 0/0 | 2303 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0005c0011t0001 | 0/0 | 2303 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0006c0008t0001 | 0/0 | 2303 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0007c0009t0001 | 0/0 | 2303 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0008c0010t0001 | 0/0 | 2303 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0009c0006t0009 | 0/0 | 2303 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| a0010c0013t0001 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | CTTAG others(2298): Show |
chr2 | 112133385 | 112193218 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0017 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0069 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0004g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0008g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0008g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0010g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0011g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0012g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0001t0013g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0005t0007g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0007t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0001c0012t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0002c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0002c0002t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0003c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0003c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0003c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0004c0004t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0005c0011t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0006c0008t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0007c0009t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0008c0010t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0009c0006t0009g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| a0010c0013t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0107 | EUR | GBR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | GBR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0077 | EUR | GBR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0129 | EUR | FIN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00280 | hp2 | a0001 | c0001 | t0010 | g0210 | EUR | FIN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | FIN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0033 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01169 | hp1 | a0005 | c0011 | t0001 | g0248 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01257 | hp1 | a0004 | c0004 | t0002 | g0026 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01258 | hp1 | a0004 | c0004 | t0002 | g0026 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | IBS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | IBS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0054 | EUR | IBS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0082 | EUR | IBS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0017 | EUR | IBS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0136 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01884 | hp2 | a0003 | c0003 | t0001 | g0042 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01891 | hp2 | a0002 | c0002 | t0003 | g0145 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0127 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0125 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01934 | hp2 | a0006 | c0008 | t0001 | g0114 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01975 | hp1 | a0007 | c0009 | t0001 | g0078 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CDX | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | CDX | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0123 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0286 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0126 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0288 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0169 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0128 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0282 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0292 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0062 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0293 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0272 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03225 | hp2 | a0001 | c0001 | t0013 | g0289 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03239 | hp1 | a0001 | c0007 | t0001 | g0075 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0201 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03490 | hp2 | a0001 | c0005 | t0007 | g0020 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03491 | hp1 | a0008 | c0010 | t0001 | g0263 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03492 | hp1 | a0001 | c0005 | t0007 | g0020 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03516 | hp1 | a0001 | c0012 | t0001 | g0157 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0234 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03704 | hp1 | a0009 | c0006 | t0009 | g0290 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0086 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0134 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0131 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0067 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | YRI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0148 | AFR | YRI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0233 | AFR | YRI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18969 | hp1 | a0010 | c0013 | t0001 | g0221 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0072 | AFR | LWK | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19043 | hp1 | a0001 | c0001 | t0012 | g0300 | AFR | LWK | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | LWK | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19065 | hp1 | a0001 | c0001 | t0011 | g0003 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | TSI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | TSI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA20805 | hp1 | a0002 | c0002 | t0003 | g0064 | EUR | TSI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0280 | EUR | TSI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | USA | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | USA | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0202 | AFR | LWK | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | LWK | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0066 | REF | REF | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0069 | REF | REF | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112159787 | G | A | 1 | a0009 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.187G>A | p.Ala63Thr | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/8 | 458/2303 | 187/1320 | 63/439 | chr2 | 112159787 | |||
| chr2:112165061 | T | A | 1 | a0004 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.296T>A | p.Val99Glu | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/8 | 567/2303 | 296/1320 | 99/439 | chr2 | 112165061 | |||
| chr2:112165120 | G | A | 1 | a0002 | 6 | HG01891.hp2 HG02922.hp2 HG03486.hp1 others(3): Show |
missense_variant | MODERATE | c.355G>A | p.Val119Met | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/8 | 626/2303 | 355/1320 | 119/439 | chr2 | 112165120 | |||
| chr2:112175762 | TAGA | T | 1 | a0003 | 3 | HG01884.hp2 HG03041.hp2 NA18522.hp2 |
disruptive_inframe_deletion | MODERATE | c.458_460delAAG | p.Glu153del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/8 | 729/2303 | 458/1320 | 153/439 | INFO_REALIGN_3_PRIME | chr2 | 112175762 | ||
| chr2:112181760 | C | G | 1 | a0010 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.554C>G | p.Ala185Gly | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/8 | 825/2303 | 554/1320 | 185/439 | chr2 | 112181760 | |||
| chr2:112181861 | G | A | 1 | a0006 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.655G>A | p.Asp219Asn | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/8 | 926/2303 | 655/1320 | 219/439 | chr2 | 112181861 | |||
| chr2:112182833 | G | A | 1 | a0007 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.713G>A | p.Arg238Gln | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/8 | 984/2303 | 713/1320 | 238/439 | chr2 | 112182833 | |||
| chr2:112182853 | G | A | 1 | a0008 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.733G>A | p.Val245Met | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/8 | 1004/2303 | 733/1320 | 245/439 | chr2 | 112182853 | |||
| chr2:112187330 | G | A | 1 | a0005 | 1 | HG01169.hp1 | missense_variant | MODERATE | c.1144G>A | p.Gly382Ser | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 8/8 | 1415/2303 | 1144/1320 | 382/439 | chr2 | 112187330 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112165119 | C | T | 1 | a0001c0005 | 2 | HG03490.hp2 HG03492.hp1 |
synonymous_variant | LOW | c.354C>T | p.Ser118Ser | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/8 | 625/2303 | 354/1320 | 118/439 | chr2 | 112165119 | |||
| chr2:112181770 | C | A | 1 | a0001c0007 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.564C>A | p.Ser188Ser | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/8 | 835/2303 | 564/1320 | 188/439 | chr2 | 112181770 | |||
| chr2:112185262 | C | T | 1 | a0001c0012 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.870C>T | p.Thr290Thr | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/8 | 1141/2303 | 870/1320 | 290/439 | chr2 | 112185262 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112138525 | C | T | 2 | a0001c0001t0008 a0001c0001t0013 |
3 | HG03225.hp2 HG03540.hp1 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-131C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/8 | 131 | chr2 | 112138525 | ||||||
| chr2:112138535 | C | T | 4 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0012 others(1): Show |
18 | HG00140.hp1 HG00280.hp1 HG01928.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-121C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/8 | 121 | chr2 | 112138535 | ||||||
| chr2:112138615 | A | C | 1 | a0001c0001t0011 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-41A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/8 | 41 | chr2 | 112138615 | ||||||
| chr2:112187611 | T | A | 15 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(12): Show |
281 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*105T>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 8/8 | 105 | chr2 | 112187611 | ||||||
| chr2:112187643 | G | A | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(3): Show |
38 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*137G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 8/8 | 137 | chr2 | 112187643 | ||||||
| chr2:112187649 | C | T | 1 | a0001c0001t0010 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*143C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 8/8 | 143 | chr2 | 112187649 | ||||||
| chr2:112187801 | C | T | 1 | a0001c0005t0007 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*295C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 8/8 | 295 | chr2 | 112187801 | ||||||
| chr2:112187874 | GC | G | 1 | a0001c0001t0005 | 6 | HG01109.hp1 HG01884.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*371delC | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 8/8 | 371 | INFO_REALIGN_3_PRIME | chr2 | 112187874 | |||||
| chr2:112188213 | C | T | 1 | a0009c0006t0009 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*707C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 8/8 | 707 | chr2 | 112188213 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112138732 | TCAGTGTC others(20): Show |
T | 3 | a0001c0001t0001g0055 a0001c0001t0002g0017 a0001c0001t0002g0054 |
4 | HG01516.hp1 HG01517.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+60_75+86delTGTC others(23): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138732 | ||||||
| chr2:112138789 | GTGTCCCT others(42): Show |
G | 29 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(26): Show |
35 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.75+80_75+128delAGG others(46): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138789 | ||||||
| chr2:112138817 | CGTCCCTC others(15): Show |
C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(209): Show |
242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.75+129_75+150delCC others(20): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138817 | ||||||
| chr2:112138817 | CGTCCCTC others(37): Show |
C | 1 | a0001c0001t0001g0296 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.75+107_75+150delCC others(42): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138817 | ||||||
| chr2:112138835 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.75+105C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112138835 | |||||||
| chr2:112138839 | T | C | 29 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(26): Show |
35 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.75+109T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112138839 | |||||||
| chr2:112138842 | CCCTCCCG others(14): Show |
C | 1 | a0001c0001t0001g0056 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.75+115_75+135delTC others(19): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138842 | ||||||
| chr2:112138860 | CTGTCCCT others(856): Show |
C | 1 | a0001c0001t0001g0071 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.75+174_75+1036del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138860 | ||||||
| chr2:112138909 | CTGTCCCG others(20): Show |
C | 1 | a0001c0001t0012g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.75+186_75+212delGC others(25): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138909 | ||||||
| chr2:112138918 | GCGCCTCT others(915): Show |
G | 1 | a0001c0001t0002g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.75+234_75+1155del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138918 | ||||||
| chr2:112138964 | C | T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(208): Show |
244 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.75+234C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112138964 | |||||||
| chr2:112139014 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+284T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139014 | |||||||
| chr2:112139041 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+311C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139041 | |||||||
| chr2:112139050 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.75+320C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139050 | |||||||
| chr2:112139068 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+338T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139068 | |||||||
| chr2:112139095 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0299 |
2 | NA18961.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.75+365C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139095 | |||||||
| chr2:112139099 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0299 |
2 | NA18961.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.75+369T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139099 | |||||||
| chr2:112139115 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.75+385C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139115 | |||||||
| chr2:112139120 | G | C | 1 | a0001c0001t0005g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+390G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139120 | |||||||
| chr2:112139120 | GGCCA | G | 10 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(7): Show |
10 | HG00323.hp1 HG01243.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+396_75+399delCC others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139120 | ||||||
| chr2:112139124 | A | AGTGTCCC others(43): Show |
1 | a0001c0001t0005g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+395_75+396insTG others(48): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139124 | ||||||
| chr2:112139124 | A | C | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | NA18946.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.75+394A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139124 | |||||||
| chr2:112139151 | C | G | 3 | a0001c0001t0001g0057 a0001c0001t0001g0299 a0001c0001t0005g0136 |
3 | HG01884.hp1 NA18961.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.75+421C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139151 | |||||||
| chr2:112139153 | C | T | 1 | a0001c0001t0005g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+423C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139153 | |||||||
| chr2:112139155 | AGTGTCCC others(16): Show |
A | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+427_75+449delTG others(21): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139155 | ||||||
| chr2:112139155 | AGTGTCCC others(178): Show |
A | 1 | a0001c0001t0001g0299 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.75+427_75+611del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139155 | ||||||
| chr2:112139184 | T | C | 1 | a0001c0001t0005g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+454T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139184 | |||||||
| chr2:112139192 | C | A | 1 | a0001c0001t0005g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+462C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139192 | |||||||
| chr2:112139205 | G | C | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+475G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139205 | |||||||
| chr2:112139207 | C | T | 1 | a0001c0001t0005g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+477C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139207 | |||||||
| chr2:112139216 | T | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
251 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.75+486T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139216 | |||||||
| chr2:112139219 | A | C | 10 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(7): Show |
10 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+489A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139219 | |||||||
| chr2:112139234 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0005g0136 |
2 | HG01884.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.75+504T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139234 | |||||||
| chr2:112139238 | T | C | 13 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0141 others(10): Show |
13 | HG00597.hp2 HG01167.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+508T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139238 | |||||||
| chr2:112139238 | T | TGTCCCTC others(20): Show |
1 | a0001c0001t0003g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+531_75+557dupCC others(25): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139238 | ||||||
| chr2:112139238 | TGTCCCTC others(344): Show |
T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG01243.hp2 HG02486.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+532_75+882del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139238 | ||||||
| chr2:112139259 | GGCCAGCG others(317): Show |
G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(5): Show |
11 | HG00639.hp2 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+535_75+858del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139259 | ||||||
| chr2:112139261 | CCAGCGTC others(20): Show |
C | 1 | a0002c0002t0002g0072 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75+558_75+584delTC others(25): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139261 | ||||||
| chr2:112139262 | CAGCGTCC others(344): Show |
C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
7 | HG01070.hp2 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+535_75+885del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139262 | ||||||
| chr2:112139265 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+535C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139265 | |||||||
| chr2:112139265 | CGTCCCTC others(344): Show |
C | 9 | a0001c0001t0001g0044 a0001c0001t0001g0143 a0001c0001t0001g0281 others(6): Show |
9 | HG01255.hp2 HG02258.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+558_75+908del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139265 | ||||||
| chr2:112139265 | CGTCCCTC others(533): Show |
C | 1 | a0001c0001t0001g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.75+558_75+1097del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139265 | ||||||
| chr2:112139270 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+540C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139270 | |||||||
| chr2:112139273 | C | A | 9 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+543C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139273 | |||||||
| chr2:112139288 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.75+558T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139288 | |||||||
| chr2:112139292 | C | T | 8 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(5): Show |
8 | HG00323.hp1 HG01243.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+562C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139292 | |||||||
| chr2:112139292 | CGTCCCTC others(452): Show |
C | 1 | a0002c0002t0003g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.75+583_75+1041del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139292 | ||||||
| chr2:112139313 | G | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.75+583G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139313 | |||||||
| chr2:112139315 | C | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.75+585C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139315 | |||||||
| chr2:112139316 | CAGCGTCC others(290): Show |
C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.75+589_75+885del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139316 | ||||||
| chr2:112139319 | CGTCCCTC others(263): Show |
C | 1 | a0002c0002t0002g0072 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75+610_75+879del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139319 | ||||||
| chr2:112139319 | CGTCCCTC others(398): Show |
C | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.75+610_75+1014del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139319 | ||||||
| chr2:112139319 | CGTCCCTC others(425): Show |
C | 1 | a0001c0001t0013g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.75+639_75+1070del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139319 | ||||||
| chr2:112139340 | C | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(89): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.75+610C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139340 | |||||||
| chr2:112139342 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.75+612C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139342 | |||||||
| chr2:112139346 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(89): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.75+616T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139346 | |||||||
| chr2:112139367 | G | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(80): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.75+637G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139367 | |||||||
| chr2:112139369 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(81): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.75+639T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139369 | |||||||
| chr2:112139373 | T | C | 10 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(7): Show |
10 | HG00323.hp1 HG01243.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+643T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139373 | |||||||
| chr2:112139394 | G | C | 2 | a0001c0001t0001g0103 a0001c0001t0005g0136 |
2 | HG01433.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.75+664G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139394 | |||||||
| chr2:112139396 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(76): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.75+666C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139396 | |||||||
| chr2:112139400 | T | C | 9 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+670T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139400 | |||||||
| chr2:112139421 | G | C | 9 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+691G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139421 | |||||||
| chr2:112139421 | GGCCAGTG others(501): Show |
G | 1 | a0001c0001t0001g0013 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.75+705_75+1212del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139421 | ||||||
| chr2:112139423 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.75+693C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139423 | |||||||
| chr2:112139427 | TGTCCCTC others(101): Show |
T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(69): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.75+705_75+812del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139427 | ||||||
| chr2:112139427 | TGTCCCTC others(128): Show |
T | 1 | a0001c0001t0003g0031 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.75+705_75+839del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139427 | ||||||
| chr2:112139435 | A | C | 19 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(16): Show |
19 | HG00323.hp1 HG01243.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.75+705A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139435 | |||||||
| chr2:112139448 | G | C | 2 | a0003c0003t0001g0148 a0003c0003t0001g0292 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.75+718G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139448 | |||||||
| chr2:112139450 | T | C | 9 | a0001c0001t0001g0073 a0001c0001t0001g0103 a0001c0001t0003g0149 others(6): Show |
9 | HG01433.hp2 HG01884.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+720T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139450 | |||||||
| chr2:112139450 | TCAGTGTC others(128): Show |
C | 1 | a0001c0001t0003g0032 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.75+720_75+854del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139450 | |||||||
| chr2:112139450 | TCAGTGTC others(128): Show |
T | 1 | a0001c0001t0001g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.75+882_75+1016del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139450 | ||||||
| chr2:112139454 | T | C | 1 | a0001c0001t0003g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.75+724T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139454 | |||||||
| chr2:112139462 | C | A | 5 | a0001c0001t0001g0073 a0001c0001t0003g0149 a0001c0001t0003g0286 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+732C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139462 | |||||||
| chr2:112139475 | G | C | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+745G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139475 | |||||||
| chr2:112139477 | C | T | 5 | a0001c0001t0001g0073 a0001c0001t0003g0149 a0001c0001t0003g0286 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+747C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139477 | |||||||
| chr2:112139478 | T | C | 19 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(16): Show |
19 | HG00323.hp1 HG01243.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.75+748T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139478 | |||||||
| chr2:112139481 | T | C | 2 | a0001c0001t0001g0299 a0001c0001t0003g0149 |
2 | HG02818.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.75+751T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139481 | |||||||
| chr2:112139485 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+755C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139485 | |||||||
| chr2:112139489 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.75+759C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139489 | |||||||
| chr2:112139502 | G | C | 2 | a0003c0003t0001g0148 a0003c0003t0001g0292 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.75+772G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139502 | |||||||
| chr2:112139502 | GGCCAGCG others(74): Show |
G | 1 | a0001c0001t0001g0103 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.75+778_75+858delCG others(79): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139502 | ||||||
| chr2:112139505 | C | T | 5 | a0001c0001t0001g0073 a0001c0001t0003g0149 a0001c0001t0003g0286 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+775C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139505 | |||||||
| chr2:112139508 | C | T | 16 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(13): Show |
16 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.75+778C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139508 | |||||||
| chr2:112139508 | CGTCCCTC others(101): Show |
C | 1 | a0001c0001t0003g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.75+801_75+908del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139508 | ||||||
| chr2:112139516 | C | A | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+786C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139516 | |||||||
| chr2:112139516 | C | CCGCCTCT others(15): Show |
1 | a0001c0001t0005g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+797_75+798insCC others(20): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139516 | ||||||
| chr2:112139529 | G | GGCCAGTG others(42): Show |
1 | a0003c0003t0001g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+800_75+801insCC others(47): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139529 | ||||||
| chr2:112139529 | G | T | 1 | a0001c0001t0005g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+799G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139529 | |||||||
| chr2:112139531 | T | C | 15 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(12): Show |
15 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+801T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139531 | |||||||
| chr2:112139531 | TCAGCGTC others(47): Show |
T | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+805_75+858delCG others(52): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139531 | ||||||
| chr2:112139535 | C | T | 11 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(8): Show |
11 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+805C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139535 | |||||||
| chr2:112139543 | C | CCGCCTCT others(69): Show |
1 | a0001c0001t0001g0058 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.75+825_75+826insCG others(74): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139543 | ||||||
| chr2:112139543 | C | CCGCCTCT others(15): Show |
1 | a0003c0003t0001g0292 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.75+824_75+825insCC others(20): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139543 | ||||||
| chr2:112139556 | G | C | 11 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(8): Show |
11 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+826G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139556 | |||||||
| chr2:112139558 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+828C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139558 | |||||||
| chr2:112139558 | CCAGCGTC others(101): Show |
C | 3 | a0001c0001t0003g0286 a0001c0001t0003g0287 a0001c0001t0005g0288 |
3 | HG02451.hp2 HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.75+853_75+960del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139558 | ||||||
| chr2:112139562 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(79): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.75+832C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139562 | |||||||
| chr2:112139562 | CGTCCCTC others(182): Show |
C | 1 | a0001c0001t0001g0299 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.75+883_75+1071del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139562 | ||||||
| chr2:112139570 | C | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(69): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.75+840C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139570 | |||||||
| chr2:112139570 | C | CCGCCTCT others(42): Show |
4 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0002g0060 others(1): Show |
4 | HG03098.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+852_75+853insGG others(47): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139570 | ||||||
| chr2:112139583 | C | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(76): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.75+853C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139583 | |||||||
| chr2:112139583 | C | T | 1 | a0001c0001t0005g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+853C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139583 | |||||||
| chr2:112139585 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(70): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.75+855C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139585 | |||||||
| chr2:112139586 | CAGTGTCC others(20): Show |
C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(5): Show |
11 | HG00639.hp2 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+883_75+909delTA others(25): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139586 | ||||||
| chr2:112139589 | T | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0073 a0001c0001t0005g0136 |
3 | HG01243.hp1 HG01884.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.75+859T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139589 | |||||||
| chr2:112139597 | C | A | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0003g0031 others(1): Show |
4 | HG01192.hp1 HG01255.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+867C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139597 | |||||||
| chr2:112139608 | CAGGCT | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+881_75+885delGC others(3): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139608 | ||||||
| chr2:112139610 | G | C | 5 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0073 others(2): Show |
5 | HG03017.hp2 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+880G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139610 | |||||||
| chr2:112139612 | C | T | 1 | a0001c0001t0003g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+882C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139612 | |||||||
| chr2:112139613 | T | C | 14 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(11): Show |
14 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+883T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139613 | |||||||
| chr2:112139614 | A | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+884A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139614 | |||||||
| chr2:112139615 | G | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+885G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139615 | |||||||
| chr2:112139616 | T | C | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+886T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139616 | |||||||
| chr2:112139622 | T | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+892T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139622 | |||||||
| chr2:112139624 | C | A | 1 | a0003c0003t0001g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+894C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139624 | |||||||
| chr2:112139624 | C | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+894C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139624 | |||||||
| chr2:112139637 | G | C | 2 | a0001c0001t0003g0067 a0001c0001t0005g0136 |
2 | HG01884.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.75+907G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139637 | |||||||
| chr2:112139637 | G | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+907G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139637 | |||||||
| chr2:112139639 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG02896.hp2 HG03017.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+909C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139639 | |||||||
| chr2:112139643 | C | T | 10 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0073 others(7): Show |
10 | HG00323.hp1 HG01884.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+913C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139643 | |||||||
| chr2:112139651 | C | A | 1 | a0003c0003t0001g0292 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.75+921C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139651 | |||||||
| chr2:112139664 | G | C | 6 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0065 others(3): Show |
6 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+934G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139664 | |||||||
| chr2:112139666 | T | C | 15 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(12): Show |
15 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+936T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139666 | |||||||
| chr2:112139670 | C | T | 9 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0065 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+940C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139670 | |||||||
| chr2:112139673 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.75+943C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139673 | |||||||
| chr2:112139691 | G | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(2): Show |
5 | HG01243.hp1 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+961G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139691 | |||||||
| chr2:112139693 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0005g0136 others(1): Show |
4 | HG00323.hp1 HG01884.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+963C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139693 | |||||||
| chr2:112139697 | C | T | 11 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(8): Show |
11 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+967C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139697 | |||||||
| chr2:112139697 | CGTCCCTC others(47): Show |
C | 6 | a0001c0001t0001g0143 a0001c0001t0001g0281 a0001c0001t0001g0283 others(3): Show |
6 | HG01255.hp2 HG03041.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+1017_75+1070del others(54): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139697 | ||||||
| chr2:112139718 | C | G | 8 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0065 others(5): Show |
8 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+988C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139718 | |||||||
| chr2:112139720 | C | T | 7 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0065 others(4): Show |
7 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+990C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139720 | |||||||
| chr2:112139724 | T | C | 2 | a0003c0003t0001g0148 a0003c0003t0001g0292 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.75+994T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139724 | |||||||
| chr2:112139727 | C | T | 1 | a0009c0006t0009g0290 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.75+997C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139727 | |||||||
| chr2:112139745 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+1015G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139745 | |||||||
| chr2:112139747 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.75+1017T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139747 | |||||||
| chr2:112139751 | T | C | 169 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
198 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.75+1021T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139751 | |||||||
| chr2:112139771 | A | C | 1 | a0001c0001t0003g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+1041A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139771 | |||||||
| chr2:112139772 | C | G | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(9): Show |
12 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+1042C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139772 | |||||||
| chr2:112139774 | C | T | 9 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0063 others(6): Show |
9 | HG00323.hp1 HG01884.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1044C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139774 | |||||||
| chr2:112139784 | T | G | 1 | a0001c0001t0003g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+1054T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139784 | |||||||
| chr2:112139786 | C | G | 1 | a0001c0001t0003g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+1056C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139786 | |||||||
| chr2:112139788 | G | A | 1 | a0001c0001t0005g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+1058G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139788 | |||||||
| chr2:112139788 | G | GCCTCTCT others(20): Show |
1 | a0001c0001t0001g0058 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.75+1070_75+1071ins others(27): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139788 | ||||||
| chr2:112139799 | G | C | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1069G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139799 | |||||||
| chr2:112139799 | G | T | 1 | a0001c0001t0003g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+1069G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139799 | |||||||
| chr2:112139801 | C | CCAGTGTC others(47): Show |
4 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0002g0060 others(1): Show |
4 | HG03098.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1097_75+1098ins others(54): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139801 | ||||||
| chr2:112139801 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0065 a0001c0001t0005g0136 others(1): Show |
4 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1071C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139801 | |||||||
| chr2:112139811 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+1081T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139811 | |||||||
| chr2:112139813 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+1083C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139813 | |||||||
| chr2:112139826 | G | C | 1 | a0001c0001t0003g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+1096G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139826 | |||||||
| chr2:112139826 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+1096G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139826 | |||||||
| chr2:112139832 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.75+1102T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139832 | |||||||
| chr2:112139852 | A | C | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1122A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139852 | |||||||
| chr2:112139853 | C | G | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1123C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139853 | |||||||
| chr2:112139853 | CGCCAGTG others(69): Show |
C | 1 | a0001c0001t0003g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+1150_75+1225del others(76): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139853 | ||||||
| chr2:112139855 | C | T | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+1125C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139855 | |||||||
| chr2:112139865 | T | G | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1135T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139865 | |||||||
| chr2:112139867 | C | G | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1137C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139867 | |||||||
| chr2:112139880 | G | C | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1150G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139880 | |||||||
| chr2:112139880 | GGCCAGTG others(42): Show |
G | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+1176_75+1224del others(49): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139880 | ||||||
| chr2:112139894 | CCGCCTCT others(15): Show |
C | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1176_75+1197del others(22): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139894 | ||||||
| chr2:112139901 | T | G | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.75+1171T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139901 | |||||||
| chr2:112139905 | C | CAGG | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+1175_75+1176ins others(3): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139905 | |||||||
| chr2:112139906 | C | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1176C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139906 | |||||||
| chr2:112139907 | C | CAG | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+1177_75+1178ins others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139907 | |||||||
| chr2:112139907 | C | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1177C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139907 | |||||||
| chr2:112139914 | G | T | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1184G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139914 | |||||||
| chr2:112139916 | G | C | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1186G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139916 | |||||||
| chr2:112139916 | GCGCCTCT others(20): Show |
G | 1 | a0001c0001t0001g0229 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.75+1199_75+1225del others(27): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139916 | ||||||
| chr2:112139918 | G | A | 1 | a0001c0001t0005g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.75+1188G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139918 | |||||||
| chr2:112139929 | T | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(107): Show |
128 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.75+1199T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139929 | |||||||
| chr2:112139929 | T | G | 8 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+1199T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139929 | |||||||
| chr2:112139935 | T | C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG03017.hp2 NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1205T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139935 | |||||||
| chr2:112139938 | C | G | 5 | a0001c0001t0001g0138 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG00597.hp2 NA18950.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+1208C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139938 | |||||||
| chr2:112139956 | C | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(108): Show |
129 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.75+1226C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139956 | |||||||
| chr2:112139958 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+1228C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139958 | |||||||
| chr2:112139962 | T | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(106): Show |
127 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.75+1232T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139962 | |||||||
| chr2:112139962 | TGTCCCTC others(47): Show |
T | 1 | a0001c0001t0001g0074 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.75+1280_75+1333del others(54): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139962 | ||||||
| chr2:112139980 | C | G | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.75+1250C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139980 | |||||||
| chr2:112139983 | G | C | 1 | a0001c0001t0001g0229 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.75+1253G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139983 | |||||||
| chr2:112139985 | C | T | 5 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0284 others(2): Show |
5 | HG00323.hp1 HG02723.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+1255C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139985 | |||||||
| chr2:112139989 | C | T | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(9): Show |
12 | HG00323.hp1 HG00741.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+1259C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139989 | |||||||
| chr2:112140010 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+1280G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140010 | |||||||
| chr2:112140012 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0001g0150 a0001c0001t0001g0284 others(1): Show |
4 | HG03017.hp2 NA18990.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1282T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140012 | |||||||
| chr2:112140016 | C | T | 10 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(7): Show |
10 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+1286C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140016 | |||||||
| chr2:112140037 | G | C | 5 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0284 others(2): Show |
5 | HG00323.hp1 HG02723.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+1307G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140037 | |||||||
| chr2:112140037 | G | GGCCAGCG others(20): Show |
1 | a0001c0007t0001g0075 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.75+1367_75+1393dup others(27): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112140037 | ||||||
| chr2:112140039 | C | T | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+1309C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140039 | |||||||
| chr2:112140043 | C | T | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1313C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140043 | |||||||
| chr2:112140070 | C | T | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1340C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140070 | |||||||
| chr2:112140097 | C | T | 11 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(8): Show |
11 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+1367C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140097 | |||||||
| chr2:112140097 | CGTCCCTC others(20): Show |
C | 4 | a0001c0001t0001g0135 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG00408.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1415_75+1441del others(27): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112140097 | ||||||
| chr2:112140118 | C | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1388C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140118 | |||||||
| chr2:112140124 | T | C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0151 a0001c0001t0001g0229 others(1): Show |
4 | HG02300.hp1 NA18989.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1394T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140124 | |||||||
| chr2:112140144 | A | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1414A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140144 | |||||||
| chr2:112140145 | C | G | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1415C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140145 | |||||||
| chr2:112140145 | CGCCAG | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1416_75+1420del others(5): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140145 | |||||||
| chr2:112140151 | T | C | 3 | a0001c0001t0001g0281 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | NA18939.hp1 NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1421T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140151 | |||||||
| chr2:112140157 | T | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1427T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140157 | |||||||
| chr2:112140159 | C | CCGCCTCT others(15): Show |
6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+1440_75+1441ins others(22): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112140159 | ||||||
| chr2:112140159 | C | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1429C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140159 | |||||||
| chr2:112140172 | G | C | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1442G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140172 | |||||||
| chr2:112140178 | C | T | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1448C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140178 | |||||||
| chr2:112140215 | G | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.75+1485G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140215 | |||||||
| chr2:112140233 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.75+1503G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140233 | |||||||
| chr2:112140336 | A | G | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1606A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140336 | |||||||
| chr2:112140342 | CCTT | C | 6 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0143 others(3): Show |
6 | HG02615.hp2 HG02647.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+1614_75+1616del others(3): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112140342 | ||||||
| chr2:112140392 | G | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1662G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140392 | |||||||
| chr2:112140514 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.75+1784G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140514 | |||||||
| chr2:112140551 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.75+1821G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140551 | |||||||
| chr2:112140604 | A | G | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1874A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140604 | |||||||
| chr2:112140746 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.75+2016G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140746 | |||||||
| chr2:112140927 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.75+2197G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140927 | |||||||
| chr2:112141053 | A | T | 2 | a0001c0001t0004g0134 a0001c0005t0007g0020 |
3 | HG03490.hp2 HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.75+2323A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141053 | |||||||
| chr2:112141271 | T | C | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+2541T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141271 | |||||||
| chr2:112141356 | C | T | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.75+2626C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141356 | |||||||
| chr2:112141412 | A | G | 1 | a0001c0001t0003g0049 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.75+2682A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141412 | |||||||
| chr2:112141495 | G | A | 1 | a0002c0002t0003g0064 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.75+2765G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141495 | |||||||
| chr2:112141704 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.75+2974G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141704 | |||||||
| chr2:112141861 | C | A | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
210 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.75+3131C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141861 | |||||||
| chr2:112141872 | G | A | 1 | a0001c0001t0003g0287 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.75+3142G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141872 | |||||||
| chr2:112141932 | G | A | 1 | a0001c0001t0006g0077 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.75+3202G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141932 | |||||||
| chr2:112141932 | G | T | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
210 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.75+3202G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141932 | |||||||
| chr2:112142136 | G | A | 7 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+3406G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142136 | |||||||
| chr2:112142277 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.75+3547T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142277 | |||||||
| chr2:112142338 | G | A | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(9): Show |
12 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+3608G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142338 | |||||||
| chr2:112142405 | T | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(109): Show |
131 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.75+3675T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142405 | |||||||
| chr2:112142444 | C | T | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.75+3714C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142444 | |||||||
| chr2:112142531 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.75+3801C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142531 | |||||||
| chr2:112142622 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.75+3892A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142622 | |||||||
| chr2:112142720 | C | T | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(140): Show |
165 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.75+3990C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142720 | |||||||
| chr2:112142736 | G | A | 13 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(10): Show |
15 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+4006G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142736 | |||||||
| chr2:112142741 | A | G | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(9): Show |
12 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+4011A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142741 | |||||||
| chr2:112142768 | T | TTGTGTG | 34 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
37 | HG00323.hp1 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.75+4048_75+4053dup others(6): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112142768 | ||||||
| chr2:112142768 | T | TTGTGTGT others(1): Show |
111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(108): Show |
129 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.75+4046_75+4053dup others(8): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112142768 | ||||||
| chr2:112142768 | T | TTGTGTGT others(3): Show |
4 | a0001c0001t0001g0025 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
5 | HG02602.hp1 HG03688.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+4044_75+4053dup others(10): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112142768 | ||||||
| chr2:112142772 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.75+4042G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142772 | |||||||
| chr2:112142788 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.75+4058A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142788 | |||||||
| chr2:112142848 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.75+4118G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142848 | |||||||
| chr2:112142897 | G | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | NA18946.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.75+4167G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142897 | |||||||
| chr2:112142926 | G | A | 3 | a0001c0001t0008g0233 a0001c0001t0008g0234 a0001c0001t0013g0289 |
3 | HG03225.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.75+4196G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142926 | |||||||
| chr2:112142947 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.75+4217T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142947 | |||||||
| chr2:112143232 | C | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 |
3 | HG01243.hp1 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.75+4502C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143232 | |||||||
| chr2:112143311 | T | C | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.75+4581T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143311 | |||||||
| chr2:112143338 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.75+4608G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143338 | |||||||
| chr2:112143442 | T | C | 109 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(106): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.75+4712T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143442 | |||||||
| chr2:112143468 | G | T | 1 | a0001c0001t0012g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.75+4738G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143468 | |||||||
| chr2:112143628 | G | A | 25 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(22): Show |
28 | HG00323.hp1 HG00639.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.75+4898G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143628 | |||||||
| chr2:112143683 | C | G | 1 | a0001c0001t0003g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.75+4953C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143683 | |||||||
| chr2:112143720 | T | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0235 a0002c0002t0003g0064 others(1): Show |
5 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+4990T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143720 | |||||||
| chr2:112143760 | TG | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0004g0132 |
5 | HG02056.hp1 HG02129.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+5031delG | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143760 | |||||||
| chr2:112143825 | C | T | 100 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(97): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.75+5095C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143825 | |||||||
| chr2:112143914 | A | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.75+5184A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143914 | |||||||
| chr2:112144013 | C | A | 2 | a0001c0001t0003g0031 a0001c0001t0003g0032 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.75+5283C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144013 | |||||||
| chr2:112144101 | T | C | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.75+5371T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144101 | |||||||
| chr2:112144170 | C | G | 2 | a0001c0001t0003g0031 a0001c0001t0003g0032 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.75+5440C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144170 | |||||||
| chr2:112144181 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.75+5451G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144181 | |||||||
| chr2:112144426 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.75+5696T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144426 | |||||||
| chr2:112144479 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.75+5749G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144479 | |||||||
| chr2:112144494 | T | C | 13 | a0001c0001t0001g0065 a0001c0001t0001g0122 a0001c0001t0001g0235 others(10): Show |
14 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+5764T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144494 | |||||||
| chr2:112144523 | C | CT | 6 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0164 others(3): Show |
6 | HG01496.hp2 HG01952.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+5812dupT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112144523 | ||||||
| chr2:112144523 | CTTT | C | 105 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(102): Show |
120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.75+5810_75+5812del others(3): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112144523 | ||||||
| chr2:112144623 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.75+5893C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144623 | |||||||
| chr2:112144650 | G | A | 13 | a0001c0001t0001g0065 a0001c0001t0001g0122 a0001c0001t0001g0235 others(10): Show |
14 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+5920G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144650 | |||||||
| chr2:112145140 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.75+6410G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145140 | |||||||
| chr2:112145144 | G | A | 99 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(96): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.75+6414G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145144 | |||||||
| chr2:112145165 | C | T | 1 | a0010c0013t0001g0221 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.75+6435C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145165 | |||||||
| chr2:112145166 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.75+6436G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145166 | |||||||
| chr2:112145225 | T | A | 1 | a0001c0001t0001g0013 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.75+6495T>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145225 | |||||||
| chr2:112145244 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0267 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.75+6514G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145244 | |||||||
| chr2:112145316 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.75+6586T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145316 | |||||||
| chr2:112145327 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.75+6597G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145327 | |||||||
| chr2:112145447 | C | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0080 a0001c0001t0001g0113 others(8): Show |
14 | HG00558.hp1 HG01069.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+6717C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145447 | |||||||
| chr2:112145662 | A | G | 99 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(96): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.75+6932A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145662 | |||||||
| chr2:112145744 | A | G | 5 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0220 others(2): Show |
5 | HG01167.hp1 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+7014A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145744 | |||||||
| chr2:112145891 | C | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.75+7161C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145891 | |||||||
| chr2:112145948 | C | T | 1 | a0001c0001t0005g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.75+7218C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145948 | |||||||
| chr2:112146132 | C | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.75+7402C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112146132 | |||||||
| chr2:112146260 | C | A | 1 | a0001c0001t0001g0296 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.75+7530C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112146260 | |||||||
| chr2:112146352 | C | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02027.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.75+7622C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112146352 | |||||||
| chr2:112146568 | C | CT | 12 | a0001c0001t0001g0044 a0001c0001t0001g0112 a0001c0001t0001g0217 others(9): Show |
13 | HG01175.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+7856dupT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112146568 | ||||||
| chr2:112146568 | CT | C | 21 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0039 others(18): Show |
22 | HG01099.hp2 HG01167.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.75+7856delT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112146568 | ||||||
| chr2:112147109 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.75+8379G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147109 | |||||||
| chr2:112147192 | G | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0217 |
2 | NA18960.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.75+8462G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147192 | |||||||
| chr2:112147290 | T | C | 4 | a0001c0001t0001g0122 a0001c0001t0008g0233 a0001c0001t0008g0234 others(1): Show |
4 | HG03225.hp2 HG03540.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+8560T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147290 | |||||||
| chr2:112147409 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.75+8679A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147409 | |||||||
| chr2:112147480 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.75+8750C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147480 | |||||||
| chr2:112147584 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.75+8854C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147584 | |||||||
| chr2:112147642 | C | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(2): Show |
8 | NA18941.hp2 NA18957.hp2 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+8912C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147642 | |||||||
| chr2:112147681 | C | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | NA18946.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.75+8951C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147681 | |||||||
| chr2:112147727 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.75+8997T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147727 | |||||||
| chr2:112147975 | T | G | 1 | a0001c0005t0007g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.75+9245T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147975 | |||||||
| chr2:112147983 | G | A | 5 | a0001c0001t0003g0149 a0001c0001t0003g0286 a0001c0001t0003g0287 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+9253G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147983 | |||||||
| chr2:112147992 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.75+9262G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147992 | |||||||
| chr2:112148004 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.75+9274G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112148004 | |||||||
| chr2:112148048 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.75+9318C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112148048 | |||||||
| chr2:112148068 | G | A | 2 | a0001c0001t0001g0065 a0002c0002t0003g0064 |
2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+9338G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112148068 | |||||||
| chr2:112148602 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.75+9872C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112148602 | |||||||
| chr2:112148634 | G | A | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.75+9904G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112148634 | |||||||
| chr2:112148738 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0080 others(22): Show |
28 | HG00408.hp1 HG00558.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.75+10008G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112148738 | |||||||
| chr2:112148992 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.75+10262G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112148992 | |||||||
| chr2:112149022 | C | T | 97 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(94): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.75+10292C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149022 | |||||||
| chr2:112149178 | GC | G | 15 | a0001c0001t0001g0065 a0001c0001t0001g0122 a0001c0001t0001g0146 others(12): Show |
16 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.75+10449delC | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149178 | |||||||
| chr2:112149314 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.76-10362G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149314 | |||||||
| chr2:112149596 | G | A | 16 | a0001c0001t0001g0065 a0001c0001t0001g0122 a0001c0001t0001g0146 others(13): Show |
18 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.76-10080G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149596 | |||||||
| chr2:112149629 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-10047G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149629 | |||||||
| chr2:112149645 | G | C | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-10031G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149645 | |||||||
| chr2:112149687 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.76-9989T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149687 | |||||||
| chr2:112149976 | G | C | 1 | a0001c0001t0001g0281 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.76-9700G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149976 | |||||||
| chr2:112149997 | A | C | 1 | a0001c0001t0001g0214 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.76-9679A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149997 | |||||||
| chr2:112150036 | G | A | 97 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(94): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.76-9640G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150036 | |||||||
| chr2:112150037 | T | C | 97 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(94): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.76-9639T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150037 | |||||||
| chr2:112150145 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.76-9531C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150145 | |||||||
| chr2:112150161 | G | A | 1 | a0002c0002t0003g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.76-9515G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150161 | |||||||
| chr2:112150255 | T | G | 1 | a0001c0001t0001g0172 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.76-9421T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150255 | |||||||
| chr2:112150382 | G | GA | 19 | a0001c0001t0001g0013 a0001c0001t0001g0051 a0001c0001t0001g0052 others(16): Show |
20 | HG01175.hp2 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.76-9284dupA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112150382 | ||||||
| chr2:112150543 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-9133C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150543 | |||||||
| chr2:112150556 | T | C | 16 | a0001c0001t0001g0065 a0001c0001t0001g0122 a0001c0001t0001g0146 others(13): Show |
18 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.76-9120T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150556 | |||||||
| chr2:112150939 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.76-8737G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150939 | |||||||
| chr2:112151111 | G | C | 1 | a0001c0001t0001g0079 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.76-8565G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151111 | |||||||
| chr2:112151127 | G | A | 1 | a0004c0004t0002g0026 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.76-8549G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151127 | |||||||
| chr2:112151181 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0112 |
2 | NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.76-8495G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151181 | |||||||
| chr2:112151190 | C | T | 2 | a0003c0003t0001g0148 a0003c0003t0001g0292 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.76-8486C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151190 | |||||||
| chr2:112151215 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.76-8461C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151215 | |||||||
| chr2:112151231 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.76-8445A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151231 | |||||||
| chr2:112151243 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-8433C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151243 | |||||||
| chr2:112151335 | C | G | 1 | a0001c0001t0006g0129 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.76-8341C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151335 | |||||||
| chr2:112151513 | C | G | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-8163C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151513 | |||||||
| chr2:112151566 | T | C | 97 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(94): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.76-8110T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151566 | |||||||
| chr2:112151627 | A | G | 5 | a0001c0001t0001g0232 a0001c0001t0001g0242 a0001c0001t0001g0265 others(2): Show |
5 | HG01175.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-8049A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151627 | |||||||
| chr2:112151898 | G | T | 1 | a0002c0002t0003g0064 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.76-7778G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151898 | |||||||
| chr2:112152002 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-7674C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152002 | |||||||
| chr2:112152079 | T | A | 4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | NA18942.hp1 NA18999.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-7597T>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152079 | |||||||
| chr2:112152171 | C | T | 1 | a0001c0005t0007g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.76-7505C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152171 | |||||||
| chr2:112152282 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-7394G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152282 | |||||||
| chr2:112152318 | G | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | NA18946.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.76-7358G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152318 | |||||||
| chr2:112152465 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.76-7211G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152465 | |||||||
| chr2:112152467 | C | A | 1 | a0002c0002t0003g0064 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.76-7209C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152467 | |||||||
| chr2:112152467 | C | T | 96 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(93): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.76-7209C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152467 | |||||||
| chr2:112152482 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0164 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.76-7194C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152482 | |||||||
| chr2:112152523 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.76-7153G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152523 | |||||||
| chr2:112152813 | G | T | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-6863G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152813 | |||||||
| chr2:112152887 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-6789T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152887 | |||||||
| chr2:112152911 | T | C | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | NA18954.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.76-6765T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152911 | |||||||
| chr2:112152927 | A | G | 2 | a0001c0001t0001g0065 a0002c0002t0003g0064 |
2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.76-6749A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152927 | |||||||
| chr2:112153079 | T | C | 1 | a0002c0002t0002g0072 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-6597T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153079 | |||||||
| chr2:112153089 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.76-6587T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153089 | |||||||
| chr2:112153133 | G | A | 2 | a0001c0001t0001g0065 a0002c0002t0003g0064 |
2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.76-6543G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153133 | |||||||
| chr2:112153147 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0164 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.76-6529C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153147 | |||||||
| chr2:112153199 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.76-6477C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153199 | |||||||
| chr2:112153254 | A | G | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-6422A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153254 | |||||||
| chr2:112153328 | C | T | 1 | a0001c0005t0007g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.76-6348C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153328 | |||||||
| chr2:112153540 | G | A | 1 | a0001c0001t0004g0132 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.76-6136G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153540 | |||||||
| chr2:112153732 | G | A | 1 | a0001c0001t0001g0279 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.76-5944G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153732 | |||||||
| chr2:112153771 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.76-5905T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153771 | |||||||
| chr2:112153900 | G | A | 1 | a0001c0005t0007g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.76-5776G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153900 | |||||||
| chr2:112153924 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.76-5752T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153924 | |||||||
| chr2:112153955 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.76-5721C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153955 | |||||||
| chr2:112153957 | C | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0005g0033 |
3 | HG01109.hp1 HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.76-5719C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153957 | |||||||
| chr2:112154346 | G | A | 108 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(105): Show |
122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.76-5330G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154346 | |||||||
| chr2:112154423 | C | T | 5 | a0001c0001t0001g0065 a0001c0001t0001g0144 a0001c0001t0001g0235 others(2): Show |
5 | HG00323.hp1 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-5253C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154423 | |||||||
| chr2:112154441 | C | G | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-5235C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154441 | |||||||
| chr2:112154455 | G | A | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-5221G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154455 | |||||||
| chr2:112154541 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-5135G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154541 | |||||||
| chr2:112154676 | T | C | 114 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(111): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.76-5000T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154676 | |||||||
| chr2:112154812 | T | C | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-4864T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154812 | |||||||
| chr2:112154850 | T | C | 1 | a0001c0001t0005g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-4826T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154850 | |||||||
| chr2:112154945 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.76-4731C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154945 | |||||||
| chr2:112155065 | G | T | 1 | a0001c0001t0001g0211 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.76-4611G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155065 | |||||||
| chr2:112155122 | T | G | 19 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(16): Show |
22 | HG00639.hp2 HG01070.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.76-4554T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155122 | |||||||
| chr2:112155292 | G | A | 109 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(106): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.76-4384G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155292 | |||||||
| chr2:112155315 | C | T | 1 | a0001c0001t0010g0210 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.76-4361C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155315 | |||||||
| chr2:112155401 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.76-4275C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155401 | |||||||
| chr2:112155440 | C | T | 11 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0149 others(8): Show |
12 | HG01257.hp1 HG01258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-4236C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155440 | |||||||
| chr2:112155449 | G | A | 3 | a0001c0001t0008g0233 a0001c0001t0008g0234 a0001c0001t0013g0289 |
3 | HG03225.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.76-4227G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155449 | |||||||
| chr2:112155709 | C | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG02132.hp1 NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.76-3967C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155709 | |||||||
| chr2:112155745 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.76-3931G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155745 | |||||||
| chr2:112155753 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0235 |
2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.76-3923A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155753 | |||||||
| chr2:112155809 | C | T | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-3867C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155809 | |||||||
| chr2:112155853 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-3823C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155853 | |||||||
| chr2:112155877 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-3799C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155877 | |||||||
| chr2:112155924 | G | A | 107 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(104): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-3752G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155924 | |||||||
| chr2:112156077 | C | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0150 a0001c0001t0001g0165 others(10): Show |
15 | HG00558.hp2 HG01978.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.76-3599C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156077 | |||||||
| chr2:112156099 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.76-3577C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156099 | |||||||
| chr2:112156160 | C | G | 4 | a0001c0001t0001g0034 a0001c0001t0002g0017 a0001c0001t0002g0054 others(1): Show |
5 | HG01192.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-3516C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156160 | |||||||
| chr2:112156332 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-3344T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156332 | |||||||
| chr2:112156362 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.76-3314A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156362 | |||||||
| chr2:112156385 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.76-3291A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156385 | |||||||
| chr2:112156390 | C | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0027 others(50): Show |
63 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.76-3286C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156390 | |||||||
| chr2:112156426 | T | C | 1 | a0001c0005t0007g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.76-3250T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156426 | |||||||
| chr2:112156528 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.76-3148T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156528 | |||||||
| chr2:112156602 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0203 |
2 | HG02027.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.76-3074G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156602 | |||||||
| chr2:112156681 | C | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0235 |
2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.76-2995C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156681 | |||||||
| chr2:112156752 | G | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0027 others(50): Show |
63 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.76-2924G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156752 | |||||||
| chr2:112156784 | C | G | 1 | a0001c0001t0001g0084 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.76-2892C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156784 | |||||||
| chr2:112156901 | ATTCCCAC others(12): Show |
A | 1 | a0001c0001t0001g0283 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.76-2774_76-2756del others(19): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156901 | |||||||
| chr2:112156962 | C | T | 2 | a0001c0001t0001g0065 a0002c0002t0003g0064 |
2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.76-2714C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156962 | |||||||
| chr2:112157032 | G | C | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-2644G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157032 | |||||||
| chr2:112157107 | C | T | 6 | a0001c0001t0001g0237 a0001c0001t0001g0264 a0001c0001t0001g0267 others(3): Show |
6 | HG00099.hp2 HG00741.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-2569C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157107 | |||||||
| chr2:112157108 | A | G | 6 | a0001c0001t0001g0237 a0001c0001t0001g0264 a0001c0001t0001g0267 others(3): Show |
6 | HG00099.hp2 HG00741.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-2568A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157108 | |||||||
| chr2:112157114 | A | T | 6 | a0001c0001t0001g0237 a0001c0001t0001g0264 a0001c0001t0001g0267 others(3): Show |
6 | HG00099.hp2 HG00741.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-2562A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157114 | |||||||
| chr2:112157190 | C | T | 1 | a0002c0002t0002g0072 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-2486C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157190 | |||||||
| chr2:112157235 | C | T | 3 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0002g0169 |
3 | HG02922.hp2 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.76-2441C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157235 | |||||||
| chr2:112157246 | T | G | 1 | a0001c0001t0010g0210 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.76-2430T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157246 | |||||||
| chr2:112157553 | C | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0027 others(38): Show |
50 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.76-2123C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157553 | |||||||
| chr2:112157673 | G | C | 1 | a0001c0001t0001g0247 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.76-2003G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157673 | |||||||
| chr2:112157718 | G | C | 107 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(104): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-1958G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157718 | |||||||
| chr2:112157746 | G | A | 107 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(104): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-1930G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157746 | |||||||
| chr2:112157747 | A | C | 107 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(104): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-1929A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157747 | |||||||
| chr2:112157864 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-1812G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157864 | |||||||
| chr2:112157902 | C | CT | 21 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(18): Show |
24 | HG00639.hp2 HG01070.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.76-1760dupT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112157902 | ||||||
| chr2:112157957 | C | T | 11 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0149 others(8): Show |
12 | HG01257.hp1 HG01258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-1719C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157957 | |||||||
| chr2:112158151 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.76-1525C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158151 | |||||||
| chr2:112158177 | G | T | 48 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0027 others(45): Show |
58 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.76-1499G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158177 | |||||||
| chr2:112158187 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-1489G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158187 | |||||||
| chr2:112158232 | A | G | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0280 |
3 | HG00741.hp2 NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.76-1444A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158232 | |||||||
| chr2:112158244 | TTTG | T | 12 | a0001c0001t0001g0109 a0001c0001t0001g0146 a0001c0001t0001g0147 others(9): Show |
13 | HG01257.hp1 HG01258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.76-1417_76-1415del others(3): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112158244 | ||||||
| chr2:112158500 | G | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0144 a0001c0001t0001g0235 others(1): Show |
4 | HG00323.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-1176G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158500 | |||||||
| chr2:112158560 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0164 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.76-1116C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158560 | |||||||
| chr2:112158596 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-1080C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158596 | |||||||
| chr2:112158597 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.76-1079G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158597 | |||||||
| chr2:112158719 | A | G | 273 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(270): Show |
312 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.76-957A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158719 | |||||||
| chr2:112158920 | C | T | 1 | a0001c0001t0004g0132 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.76-756C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158920 | |||||||
| chr2:112159039 | A | T | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-637A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112159039 | |||||||
| chr2:112159191 | G | GT | 103 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(100): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.76-474dupT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112159191 | ||||||
| chr2:112159254 | T | G | 2 | a0001c0001t0001g0065 a0002c0002t0003g0064 |
2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.76-422T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112159254 | |||||||
| chr2:112159282 | G | GC | 93 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(90): Show |
106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.76-391dupC | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112159282 | ||||||
| chr2:112159292 | T | C | 2 | a0001c0001t0001g0247 a0005c0011t0001g0248 |
2 | HG00140.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.76-384T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112159292 | |||||||
| chr2:112159390 | A | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0203 |
2 | HG02027.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.76-286A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112159390 | |||||||
| chr2:112159525 | G | C | 107 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(104): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-151G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112159525 | |||||||
| chr2:112159647 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.76-29G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112159647 | |||||||
| chr2:112159845 | C | T | 1 | a0001c0005t0007g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.235+10C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112159845 | |||||||
| chr2:112159852 | G | A | 1 | a0001c0005t0007g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.235+17G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112159852 | |||||||
| chr2:112159940 | A | G | 2 | a0001c0001t0006g0077 a0001c0001t0006g0129 |
2 | HG00140.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.235+105A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112159940 | |||||||
| chr2:112159997 | A | T | 2 | a0001c0001t0001g0065 a0002c0002t0003g0064 |
2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.235+162A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112159997 | |||||||
| chr2:112160001 | A | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0235 a0002c0002t0003g0064 |
3 | HG00323.hp1 HG02970.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.235+166A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160001 | |||||||
| chr2:112160030 | G | A | 10 | a0001c0001t0001g0070 a0001c0001t0001g0146 a0001c0001t0003g0149 others(7): Show |
10 | HG02451.hp2 HG02602.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.235+195G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160030 | |||||||
| chr2:112160043 | T | C | 9 | a0001c0001t0001g0146 a0001c0001t0003g0149 a0001c0001t0003g0286 others(6): Show |
9 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.235+208T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160043 | |||||||
| chr2:112160043 | T | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0236 |
3 | HG02145.hp1 HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.235+208T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160043 | |||||||
| chr2:112160048 | T | G | 1 | a0001c0001t0001g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.235+213T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160048 | |||||||
| chr2:112160051 | C | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0146 a0001c0001t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02602.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.235+216C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160051 | |||||||
| chr2:112160053 | C | G | 1 | a0001c0001t0005g0240 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.235+218C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160053 | |||||||
| chr2:112160092 | G | A | 5 | a0001c0001t0003g0149 a0001c0001t0003g0286 a0001c0001t0003g0287 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+257G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160092 | |||||||
| chr2:112160117 | C | A | 2 | a0001c0001t0001g0065 a0002c0002t0003g0064 |
2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.235+282C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160117 | |||||||
| chr2:112160136 | G | A | 6 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0211 others(3): Show |
6 | HG01109.hp1 HG02083.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+301G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160136 | |||||||
| chr2:112160139 | C | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0232 others(1): Show |
4 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+304C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160139 | |||||||
| chr2:112160145 | C | A | 2 | a0003c0003t0001g0148 a0003c0003t0001g0292 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.235+310C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160145 | |||||||
| chr2:112160145 | C | T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0008c0010t0001g0263 |
3 | HG03239.hp2 HG03491.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.235+310C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160145 | |||||||
| chr2:112160158 | T | C | 21 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(18): Show |
24 | HG00639.hp2 HG01070.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.235+323T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160158 | |||||||
| chr2:112160181 | G | T | 1 | a0008c0010t0001g0263 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.235+346G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160181 | |||||||
| chr2:112160192 | T | G | 17 | a0001c0001t0001g0024 a0001c0001t0001g0058 a0001c0001t0001g0059 others(14): Show |
18 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.235+357T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160192 | |||||||
| chr2:112160211 | C | G | 8 | a0001c0001t0001g0065 a0001c0001t0001g0160 a0001c0001t0001g0161 others(5): Show |
8 | HG00323.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.235+376C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160211 | |||||||
| chr2:112160225 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.235+390C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160225 | |||||||
| chr2:112160263 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.235+428G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160263 | |||||||
| chr2:112160273 | G | A | 4 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0284 others(1): Show |
4 | HG00558.hp1 HG02132.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+438G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160273 | |||||||
| chr2:112160285 | G | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | NA18994.hp1 NA19030.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.235+450G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160285 | |||||||
| chr2:112160640 | ACACACGC others(5): Show |
A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.235+825_235+836del others(12): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160640 | ||||||
| chr2:112160642 | ACACGCGC others(11): Show |
A | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.235+813_235+830del others(18): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160642 | ||||||
| chr2:112160648 | GCACGCAC others(11): Show |
G | 4 | a0001c0001t0001g0235 a0001c0005t0007g0020 a0002c0002t0002g0072 others(1): Show |
5 | HG02970.hp1 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+825_235+842del others(18): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160648 | ||||||
| chr2:112160679 | G | C | 1 | a0001c0005t0007g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.235+844G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160679 | |||||||
| chr2:112160688 | ACACGCAC others(5): Show |
A | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+865_235+876del others(12): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160688 | ||||||
| chr2:112160704 | GCA | G | 118 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(115): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.235+878_235+879del others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160704 | ||||||
| chr2:112160718 | A | G | 12 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0232 others(9): Show |
13 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.235+883A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160718 | |||||||
| chr2:112160720 | G | A | 18 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(15): Show |
20 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.235+885G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160720 | |||||||
| chr2:112160720 | GCGCACAC others(9): Show |
G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0182 a0001c0001t0001g0273 |
3 | HG02083.hp1 NA18968.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.235+893_235+908del others(16): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160720 | ||||||
| chr2:112160726 | A | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0002g0043 others(5): Show |
11 | HG01070.hp2 HG01346.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.235+891A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160726 | |||||||
| chr2:112160728 | G | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0002g0043 others(5): Show |
11 | HG01070.hp2 HG01346.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.235+893G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160728 | |||||||
| chr2:112160732 | G | A | 1 | a0001c0001t0004g0132 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.235+897G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160732 | |||||||
| chr2:112160734 | A | G | 1 | a0001c0001t0004g0132 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.235+899A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160734 | |||||||
| chr2:112160736 | A | ACGCACAC others(1): Show |
17 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(14): Show |
19 | HG01243.hp1 HG01257.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.235+908_235+909ins others(8): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160736 | ||||||
| chr2:112160738 | GCA | G | 96 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(93): Show |
108 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.235+909_235+910del others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160738 | ||||||
| chr2:112160740 | A | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0235 others(4): Show |
10 | HG01070.hp2 HG01346.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.235+905A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160740 | |||||||
| chr2:112160744 | A | G | 15 | a0001c0001t0001g0122 a0001c0001t0001g0250 a0001c0001t0001g0264 others(12): Show |
15 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(12): Show |
intron_variant | MODIFIER | c.235+909A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160744 | |||||||
| chr2:112160744 | ACG | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0002g0043 others(1): Show |
5 | HG01070.hp2 HG01346.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+913_235+914del others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160744 | ||||||
| chr2:112160746 | G | A | 23 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(20): Show |
25 | HG00408.hp1 HG01243.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.235+911G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160746 | |||||||
| chr2:112160746 | GCGCACGC others(5): Show |
G | 1 | a0001c0001t0001g0120 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.235+923_235+934del others(12): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160746 | ||||||
| chr2:112160747 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.235+912C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160747 | |||||||
| chr2:112160747 | CGCACGCA others(19): Show |
C | 5 | a0001c0001t0001g0250 a0001c0001t0001g0264 a0001c0001t0004g0018 others(2): Show |
7 | HG00099.hp2 HG01884.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+913_235+938del others(26): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160747 | |||||||
| chr2:112160748 | G | A | 13 | a0001c0001t0001g0122 a0001c0001t0004g0125 a0001c0001t0004g0127 others(10): Show |
13 | HG00140.hp1 HG00280.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.235+913G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160748 | |||||||
| chr2:112160750 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0235 |
2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.235+915A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160750 | |||||||
| chr2:112160750 | ACG | A | 93 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(90): Show |
105 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.235+917_235+918del others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160750 | ||||||
| chr2:112160752 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.235+917G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160752 | |||||||
| chr2:112160753 | CACACACG others(13): Show |
C | 12 | a0001c0001t0001g0122 a0001c0001t0004g0125 a0001c0001t0004g0127 others(9): Show |
12 | HG00140.hp1 HG00280.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+921_235+940del others(20): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160753 | ||||||
| chr2:112160754 | A | G | 3 | a0001c0001t0001g0235 a0001c0001t0002g0082 a0001c0001t0004g0132 |
3 | HG01516.hp2 HG02970.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.235+919A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160754 | |||||||
| chr2:112160754 | ACACACGC others(15): Show |
A | 1 | a0001c0001t0010g0210 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.235+938_235+959del others(22): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160754 | ||||||
| chr2:112160758 | A | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0021 others(9): Show |
15 | HG01433.hp1 HG01496.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.235+923A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160758 | |||||||
| chr2:112160760 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0021 others(8): Show |
14 | HG01433.hp1 HG01496.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.235+925G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160760 | |||||||
| chr2:112160760 | GCACGCA | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0002g0043 others(1): Show |
5 | HG01070.hp2 HG01346.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+932_235+937del others(6): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160760 | ||||||
| chr2:112160761 | C | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0021 others(8): Show |
14 | HG01433.hp1 HG01496.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.235+926C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160761 | |||||||
| chr2:112160761 | CACGCACA others(5): Show |
C | 97 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(94): Show |
109 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.235+938_235+949del others(12): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160761 | ||||||
| chr2:112160764 | GCA | G | 11 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0149 others(8): Show |
12 | HG01257.hp1 HG01258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+933_235+934del others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160764 | ||||||
| chr2:112160776 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0264 a0001c0001t0005g0136 |
3 | HG00099.hp2 HG01884.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.235+941G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160776 | |||||||
| chr2:112160782 | GCACGCAC others(21): Show |
G | 1 | a0001c0001t0001g0298 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.235+957_235+984del others(28): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160782 | ||||||
| chr2:112160792 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+957G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160792 | |||||||
| chr2:112160792 | G | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.235+957G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160792 | |||||||
| chr2:112160794 | ACACACGC others(3): Show |
A | 1 | a0001c0001t0003g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.235+965_235+974del others(10): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160794 | ||||||
| chr2:112160796 | ACACG | A | 12 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0232 others(9): Show |
13 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.235+969_235+972del others(4): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160796 | ||||||
| chr2:112160800 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+965G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160800 | |||||||
| chr2:112160800 | GCACGCAC others(3): Show |
G | 1 | a0001c0001t0001g0175 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.235+978_235+987del others(10): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160800 | ||||||
| chr2:112160803 | C | A | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+968C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160803 | |||||||
| chr2:112160808 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.235+973A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160808 | |||||||
| chr2:112160813 | CGCACACA others(3): Show |
C | 1 | a0001c0001t0001g0260 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.235+983_235+992del others(10): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160813 | ||||||
| chr2:112160818 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+983A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160818 | |||||||
| chr2:112160823 | A | C | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+988A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160823 | |||||||
| chr2:112160823 | AGCACGCA others(5): Show |
A | 1 | a0001c0001t0001g0269 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.235+996_235+1007de others(13): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160823 | ||||||
| chr2:112160826 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+991A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160826 | |||||||
| chr2:112160828 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+993G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160828 | |||||||
| chr2:112160831 | T | C | 21 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0146 others(18): Show |
24 | HG01070.hp2 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.235+996T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160831 | |||||||
| chr2:112160836 | G | A | 2 | a0002c0002t0002g0072 a0002c0002t0003g0064 |
2 | NA19030.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.235+1001G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160836 | |||||||
| chr2:112160842 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+1007A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160842 | |||||||
| chr2:112160846 | G | A | 6 | a0001c0001t0001g0235 a0001c0001t0003g0149 a0001c0001t0003g0286 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+1011G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160846 | |||||||
| chr2:112160846 | G | GCGCGCAC others(17): Show |
2 | a0002c0002t0002g0072 a0002c0002t0003g0064 |
2 | NA19030.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.235+1014_235+1015i others(26): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160846 | ||||||
| chr2:112160848 | G | A | 5 | a0001c0001t0001g0147 a0001c0001t0008g0233 a0001c0001t0008g0234 others(2): Show |
6 | HG01257.hp1 HG01258.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+1013G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160848 | |||||||
| chr2:112160848 | G | GCACACAC others(1): Show |
3 | a0001c0001t0001g0111 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG02132.hp1 NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.235+1025_235+1032d others(10): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160848 | ||||||
| chr2:112160848 | GCA | G | 106 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(103): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.235+1031_235+1032d others(4): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160848 | ||||||
| chr2:112160848 | GCACA | G | 7 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(4): Show |
7 | HG01109.hp1 HG01243.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+1029_235+1032d others(6): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160848 | ||||||
| chr2:112160850 | A | ACG | 5 | a0001c0001t0003g0149 a0001c0001t0003g0286 a0001c0001t0003g0287 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+1016_235+1017i others(4): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160850 | ||||||
| chr2:112160850 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.235+1015A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160850 | |||||||
| chr2:112160852 | A | G | 3 | a0001c0001t0001g0235 a0002c0002t0002g0072 a0002c0002t0003g0064 |
3 | HG02970.hp1 NA19030.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.235+1017A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160852 | |||||||
| chr2:112160881 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.235+1046G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160881 | |||||||
| chr2:112160968 | A | C | 1 | a0001c0005t0007g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.235+1133A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160968 | |||||||
| chr2:112161216 | G | A | 1 | a0001c0001t0003g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.235+1381G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161216 | |||||||
| chr2:112161288 | T | G | 1 | a0001c0001t0003g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.235+1453T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161288 | |||||||
| chr2:112161397 | A | G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0002g0043 others(3): Show |
7 | HG01070.hp2 HG01346.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+1562A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161397 | |||||||
| chr2:112161495 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0002g0082 |
2 | HG01257.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.235+1660G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161495 | |||||||
| chr2:112161548 | C | T | 12 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0154 others(9): Show |
13 | HG01257.hp1 HG01258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.235+1713C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161548 | |||||||
| chr2:112161669 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.235+1834G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161669 | |||||||
| chr2:112161736 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+1901C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161736 | |||||||
| chr2:112161993 | T | A | 1 | a0001c0001t0001g0296 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.235+2158T>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161993 | |||||||
| chr2:112162042 | A | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0002g0043 others(4): Show |
9 | HG01070.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.235+2207A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162042 | |||||||
| chr2:112162102 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.235+2267C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162102 | |||||||
| chr2:112162290 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.235+2455G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162290 | |||||||
| chr2:112162308 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.235+2473C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162308 | |||||||
| chr2:112162318 | CT | C | 19 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(16): Show |
19 | HG00733.hp1 HG01175.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.235+2499delT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112162318 | ||||||
| chr2:112162487 | C | T | 1 | a0001c0001t0005g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.236-2514C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162487 | |||||||
| chr2:112162502 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.236-2499A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162502 | |||||||
| chr2:112162558 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.236-2443G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162558 | |||||||
| chr2:112162642 | C | T | 145 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(142): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.236-2359C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162642 | |||||||
| chr2:112162647 | C | T | 8 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(5): Show |
8 | HG01175.hp2 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-2354C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162647 | |||||||
| chr2:112162754 | A | G | 2 | a0002c0002t0002g0072 a0002c0002t0003g0064 |
2 | NA19030.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.236-2247A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162754 | |||||||
| chr2:112162766 | A | T | 114 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(111): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.236-2235A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162766 | |||||||
| chr2:112162849 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.236-2152C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162849 | |||||||
| chr2:112162891 | T | C | 2 | a0003c0003t0001g0148 a0003c0003t0001g0292 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.236-2110T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162891 | |||||||
| chr2:112163070 | C | T | 1 | a0001c0005t0007g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.236-1931C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163070 | |||||||
| chr2:112163140 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.236-1861C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163140 | |||||||
| chr2:112163189 | G | A | 10 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0149 others(7): Show |
10 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.236-1812G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163189 | |||||||
| chr2:112163272 | A | G | 3 | a0001c0001t0001g0235 a0002c0002t0002g0072 a0002c0002t0003g0064 |
3 | HG02970.hp1 NA19030.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.236-1729A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163272 | |||||||
| chr2:112163337 | A | C | 1 | a0001c0005t0007g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.236-1664A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163337 | |||||||
| chr2:112163485 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01192.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.236-1516C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163485 | |||||||
| chr2:112163723 | G | GTCAGGCT others(17): Show |
4 | a0001c0001t0001g0235 a0002c0002t0002g0072 a0002c0002t0003g0064 others(1): Show |
4 | HG01891.hp2 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-1278_236-1277i others(26): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163723 | |||||||
| chr2:112163725 | G | A | 4 | a0001c0001t0001g0235 a0002c0002t0002g0072 a0002c0002t0003g0064 others(1): Show |
4 | HG01891.hp2 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-1276G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163725 | |||||||
| chr2:112163990 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.236-1011G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163990 | |||||||
| chr2:112164036 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.236-965C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112164036 | |||||||
| chr2:112164210 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.236-791A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112164210 | |||||||
| chr2:112164213 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(80): Show |
98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.236-788G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112164213 | |||||||
| chr2:112164345 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0268 others(1): Show |
6 | NA18941.hp2 NA18957.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.236-656G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112164345 | |||||||
| chr2:112164379 | T | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
75 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.236-622T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112164379 | |||||||
| chr2:112164915 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.236-86C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112164915 | |||||||
| chr2:112164951 | G | C | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.236-50G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112164951 | |||||||
| chr2:112165529 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.406+358C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112165529 | |||||||
| chr2:112165751 | G | T | 1 | a0001c0005t0007g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.406+580G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112165751 | |||||||
| chr2:112166024 | A | AG | 23 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0058 others(20): Show |
24 | HG01070.hp2 HG01175.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.406+853_406+854ins others(1): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166024 | |||||||
| chr2:112166074 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.406+903G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166074 | |||||||
| chr2:112166094 | A | G | 1 | a0001c0001t0012g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.406+923A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166094 | |||||||
| chr2:112166153 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.406+982C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166153 | |||||||
| chr2:112166276 | C | T | 3 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0260 |
3 | HG01109.hp2 HG01515.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.406+1105C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166276 | |||||||
| chr2:112166406 | T | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(110): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.406+1235T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166406 | |||||||
| chr2:112166532 | T | C | 23 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0058 others(20): Show |
24 | HG01070.hp2 HG01175.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.406+1361T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166532 | |||||||
| chr2:112166569 | A | C | 140 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(137): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.406+1398A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166569 | |||||||
| chr2:112166592 | A | AAC | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0002g0072 others(3): Show |
6 | HG01891.hp2 HG02922.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+1423_406+1424d others(4): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112166592 | ||||||
| chr2:112166631 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.406+1460C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166631 | |||||||
| chr2:112166672 | T | C | 1 | a0004c0004t0002g0026 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.406+1501T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166672 | |||||||
| chr2:112166832 | C | T | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0002g0072 others(3): Show |
6 | HG01891.hp2 HG02922.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+1661C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166832 | |||||||
| chr2:112166931 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.406+1760G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166931 | |||||||
| chr2:112167092 | G | A | 1 | a0004c0004t0002g0026 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.406+1921G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167092 | |||||||
| chr2:112167103 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.406+1932C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167103 | |||||||
| chr2:112167192 | A | G | 27 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(24): Show |
29 | HG00639.hp2 HG01243.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.406+2021A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167192 | |||||||
| chr2:112167330 | T | C | 140 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(137): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.406+2159T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167330 | |||||||
| chr2:112167387 | TA | T | 17 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0058 others(14): Show |
18 | HG01070.hp2 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.406+2217delA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167387 | |||||||
| chr2:112167396 | G | A | 67 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(64): Show |
79 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.406+2225G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167396 | |||||||
| chr2:112167456 | T | G | 23 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0058 others(20): Show |
24 | HG01070.hp2 HG01175.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.406+2285T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167456 | |||||||
| chr2:112167486 | G | A | 7 | a0001c0001t0001g0144 a0002c0002t0001g0201 a0002c0002t0001g0202 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.406+2315G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167486 | |||||||
| chr2:112167584 | C | T | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0002g0072 others(3): Show |
6 | HG01891.hp2 HG02922.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+2413C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167584 | |||||||
| chr2:112167618 | C | T | 1 | a0002c0002t0002g0072 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.406+2447C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167618 | |||||||
| chr2:112167869 | C | CGTTAT | 21 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0138 others(18): Show |
25 | HG00099.hp1 HG00597.hp2 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.406+2747_406+2751d others(7): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | C | CGTTATGT others(3): Show |
23 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0023 others(20): Show |
27 | HG00323.hp2 HG00735.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.406+2742_406+2751d others(12): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | C | CGTTATGT others(8): Show |
27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0057 others(24): Show |
34 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.406+2737_406+2751d others(17): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | C | CGTTATGT others(13): Show |
33 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0070 others(30): Show |
36 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.406+2732_406+2751d others(22): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | C | CGTTATGT others(18): Show |
14 | a0001c0001t0001g0024 a0001c0001t0001g0073 a0001c0001t0001g0109 others(11): Show |
15 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.406+2727_406+2751d others(27): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | C | CGTTATGT others(23): Show |
7 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0079 others(4): Show |
10 | HG01175.hp1 HG01256.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.406+2722_406+2751d others(32): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | C | CGTTATGT others(28): Show |
6 | a0001c0001t0001g0101 a0001c0001t0001g0182 a0001c0001t0001g0183 others(3): Show |
6 | HG01346.hp1 HG02083.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.406+2717_406+2751d others(37): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | C | CGTTATGT others(33): Show |
1 | a0001c0001t0001g0084 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.406+2712_406+2751d others(42): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | C | CGTTATGT others(48): Show |
1 | a0001c0001t0001g0273 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.406+2751_406+2752i others(57): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | C | CGTTATGT others(12): Show |
31 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0029 others(28): Show |
34 | HG00140.hp2 HG00733.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.406+2713_406+2714i others(21): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | C | CGTTATGT others(17): Show |
43 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(40): Show |
52 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.406+2713_406+2714i others(26): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | C | CGTTATGT others(22): Show |
38 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0051 others(35): Show |
42 | HG00280.hp1 HG00741.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.406+2713_406+2714i others(31): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | C | CGTTATGT others(27): Show |
12 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0053 others(9): Show |
13 | HG00140.hp1 HG00323.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.406+2713_406+2714i others(36): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | C | CGTTATGT others(32): Show |
4 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0280 others(1): Show |
4 | HG00673.hp2 HG02074.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.406+2713_406+2714i others(41): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | C | CGTTATGT others(42): Show |
1 | a0001c0001t0001g0218 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.406+2713_406+2714i others(51): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167869 | CGTTATGT others(3): Show |
C | 1 | a0001c0001t0001g0208 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.406+2742_406+2751d others(12): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | ||||||
| chr2:112167870 | G | GTTATGTT others(7): Show |
8 | a0001c0001t0001g0037 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
10 | HG00639.hp1 HG00738.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.406+2700_406+2713d others(16): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167870 | ||||||
| chr2:112167890 | G | C | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.406+2719G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167890 | |||||||
| chr2:112167895 | G | C | 15 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0058 others(12): Show |
16 | HG01175.hp2 HG01243.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.406+2724G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167895 | |||||||
| chr2:112168129 | G | A | 9 | a0001c0001t0001g0154 a0001c0001t0003g0031 a0001c0001t0003g0032 others(6): Show |
9 | HG01891.hp2 HG02886.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+2958G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112168129 | |||||||
| chr2:112168284 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.406+3113C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112168284 | |||||||
| chr2:112168892 | C | T | 7 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0265 others(4): Show |
7 | HG01175.hp2 HG01243.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.406+3721C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112168892 | |||||||
| chr2:112168969 | G | A | 1 | a0004c0004t0002g0026 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.406+3798G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112168969 | |||||||
| chr2:112169045 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0235 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.406+3874C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169045 | |||||||
| chr2:112169133 | G | A | 1 | a0001c0001t0010g0210 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.406+3962G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169133 | |||||||
| chr2:112169213 | C | T | 17 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0058 others(14): Show |
18 | HG01070.hp2 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.406+4042C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169213 | |||||||
| chr2:112169240 | T | G | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0002g0072 others(3): Show |
6 | HG01891.hp2 HG02922.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+4069T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169240 | |||||||
| chr2:112169454 | G | A | 1 | a0001c0001t0003g0293 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.406+4283G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169454 | |||||||
| chr2:112169489 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.406+4318C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169489 | |||||||
| chr2:112169508 | G | A | 3 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0260 |
3 | HG01109.hp2 HG01515.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.406+4337G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169508 | |||||||
| chr2:112169616 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.406+4445C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169616 | |||||||
| chr2:112169771 | A | G | 19 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0058 others(16): Show |
20 | HG01070.hp2 HG01175.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.406+4600A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169771 | |||||||
| chr2:112169820 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.406+4649G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169820 | |||||||
| chr2:112169990 | T | C | 140 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(137): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.406+4819T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169990 | |||||||
| chr2:112170157 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.406+4986G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170157 | |||||||
| chr2:112170267 | C | CAGAAA | 2 | a0001c0005t0007g0020 a0004c0004t0002g0026 |
4 | HG01257.hp1 HG01258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+5113_406+5117d others(7): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112170267 | ||||||
| chr2:112170267 | CAGAAA | C | 7 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0002c0002t0001g0201 others(4): Show |
7 | HG02896.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.406+5113_406+5117d others(7): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112170267 | ||||||
| chr2:112170324 | C | T | 5 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0002g0072 others(2): Show |
5 | HG02922.hp2 HG03486.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.406+5153C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170324 | |||||||
| chr2:112170404 | G | A | 112 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(109): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.406+5233G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170404 | |||||||
| chr2:112170424 | G | A | 1 | a0004c0004t0002g0026 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.406+5253G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170424 | |||||||
| chr2:112170476 | G | A | 1 | a0001c0001t0003g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.407-5238G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170476 | |||||||
| chr2:112170544 | AAAAAG | A | 16 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0058 others(13): Show |
17 | HG01070.hp2 HG01243.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.407-5159_407-5155d others(7): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112170544 | ||||||
| chr2:112170605 | C | A | 1 | a0001c0001t0005g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.407-5109C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170605 | |||||||
| chr2:112170692 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.407-5022C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170692 | |||||||
| chr2:112170736 | T | C | 1 | a0001c0001t0003g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.407-4978T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170736 | |||||||
| chr2:112170795 | T | C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0058 others(15): Show |
19 | HG01070.hp2 HG01175.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.407-4919T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170795 | |||||||
| chr2:112171066 | A | T | 6 | a0001c0001t0001g0146 a0002c0002t0001g0201 a0002c0002t0001g0202 others(3): Show |
6 | HG02896.hp2 HG02922.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.407-4648A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171066 | |||||||
| chr2:112171238 | A | G | 121 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(118): Show |
139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.407-4476A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171238 | |||||||
| chr2:112171359 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.407-4355C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171359 | |||||||
| chr2:112171416 | GT | G | 6 | a0001c0001t0003g0149 a0001c0001t0003g0286 a0001c0001t0003g0287 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.407-4294delT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112171416 | ||||||
| chr2:112171470 | C | G | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.407-4244C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171470 | |||||||
| chr2:112171542 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.407-4172T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171542 | |||||||
| chr2:112171663 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.407-4051A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171663 | |||||||
| chr2:112171904 | A | G | 137 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(134): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.407-3810A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171904 | |||||||
| chr2:112171907 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.407-3807C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171907 | |||||||
| chr2:112171908 | G | A | 136 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(133): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.407-3806G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171908 | |||||||
| chr2:112171933 | A | G | 1 | a0001c0001t0005g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.407-3781A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171933 | |||||||
| chr2:112171937 | C | T | 1 | a0001c0001t0005g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.407-3777C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171937 | |||||||
| chr2:112171938 | A | G | 1 | a0001c0001t0005g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.407-3776A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171938 | |||||||
| chr2:112171949 | G | A | 1 | a0001c0001t0006g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.407-3765G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171949 | |||||||
| chr2:112171962 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.407-3752T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171962 | |||||||
| chr2:112172057 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.407-3657A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112172057 | |||||||
| chr2:112172219 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.407-3495T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112172219 | |||||||
| chr2:112172400 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.407-3314A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112172400 | |||||||
| chr2:112172487 | C | T | 111 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(108): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.407-3227C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112172487 | |||||||
| chr2:112172627 | C | CT | 28 | a0001c0001t0001g0048 a0001c0001t0001g0084 a0001c0001t0001g0089 others(25): Show |
28 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.407-3063dupT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112172627 | ||||||
| chr2:112172627 | CT | C | 77 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
89 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.407-3063delT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112172627 | ||||||
| chr2:112172914 | G | A | 37 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0039 others(34): Show |
42 | HG00639.hp2 HG01074.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.407-2800G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112172914 | |||||||
| chr2:112172942 | G | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.407-2772G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112172942 | |||||||
| chr2:112173058 | G | C | 5 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0243 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.407-2656G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112173058 | |||||||
| chr2:112173415 | A | G | 1 | a0001c0001t0004g0134 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.407-2299A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112173415 | |||||||
| chr2:112173613 | G | A | 5 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0243 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.407-2101G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112173613 | |||||||
| chr2:112173614 | C | G | 5 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0243 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.407-2100C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112173614 | |||||||
| chr2:112173830 | G | C | 1 | a0001c0001t0001g0255 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.407-1884G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112173830 | |||||||
| chr2:112173968 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.407-1746C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112173968 | |||||||
| chr2:112174170 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.407-1544C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174170 | |||||||
| chr2:112174177 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.407-1537C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174177 | |||||||
| chr2:112174359 | T | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(54): Show |
67 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.407-1355T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174359 | |||||||
| chr2:112174379 | A | G | 38 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0039 others(35): Show |
43 | HG00639.hp2 HG01074.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.407-1335A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174379 | |||||||
| chr2:112174473 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.407-1241G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174473 | |||||||
| chr2:112174703 | T | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0253 |
2 | HG01081.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.407-1011T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174703 | |||||||
| chr2:112174780 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.407-934G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174780 | |||||||
| chr2:112174858 | T | A | 2 | a0001c0001t0003g0243 a0001c0001t0003g0271 |
2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.407-856T>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174858 | |||||||
| chr2:112174919 | T | TA | 5 | a0001c0001t0001g0113 a0001c0001t0001g0137 a0001c0001t0001g0153 others(2): Show |
5 | HG02135.hp1 HG02135.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.407-787dupA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112174919 | ||||||
| chr2:112174932 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0004g0127 |
2 | HG00735.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.407-782T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174932 | |||||||
| chr2:112175015 | G | GA | 96 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(93): Show |
108 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.407-692dupA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112175015 | ||||||
| chr2:112175314 | A | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(100): Show |
119 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.407-400A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112175314 | |||||||
| chr2:112175548 | T | C | 8 | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0006g0077 others(5): Show |
10 | HG00140.hp1 HG00280.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.407-166T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112175548 | |||||||
| chr2:112175944 | C | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(54): Show |
67 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.532+105C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112175944 | |||||||
| chr2:112176075 | C | T | 6 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0243 others(3): Show |
6 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.532+236C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112176075 | |||||||
| chr2:112176172 | C | A | 1 | a0001c0001t0001g0104 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.532+333C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112176172 | |||||||
| chr2:112176346 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.532+507C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112176346 | |||||||
| chr2:112176418 | C | T | 4 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0243 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.532+579C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112176418 | |||||||
| chr2:112176681 | G | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0230 |
2 | NA18954.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.532+842G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112176681 | |||||||
| chr2:112176856 | C | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
129 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.532+1017C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112176856 | |||||||
| chr2:112176934 | AT | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.532+1111delT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112176934 | ||||||
| chr2:112176934 | ATT | A | 46 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0036 others(43): Show |
52 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.532+1110_532+1111d others(4): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112176934 | ||||||
| chr2:112176951 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
253 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.532+1112A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112176951 | |||||||
| chr2:112177134 | C | T | 1 | a0001c0005t0007g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.532+1295C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112177134 | |||||||
| chr2:112177474 | G | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
66 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.532+1635G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112177474 | |||||||
| chr2:112177535 | A | G | 15 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0246 others(12): Show |
17 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.532+1696A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112177535 | |||||||
| chr2:112177595 | A | G | 1 | a0001c0001t0001g0280 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.532+1756A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112177595 | |||||||
| chr2:112177950 | G | A | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
66 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.532+2111G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112177950 | |||||||
| chr2:112178008 | CA | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
228 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.532+2181delA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112178008 | ||||||
| chr2:112178147 | G | A | 4 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0163 others(1): Show |
4 | HG02258.hp2 HG02723.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.532+2308G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178147 | |||||||
| chr2:112178257 | C | CA | 21 | a0001c0001t0001g0038 a0001c0001t0001g0058 a0001c0001t0001g0059 others(18): Show |
22 | HG01074.hp2 HG01081.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.532+2429dupA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112178257 | ||||||
| chr2:112178257 | C | CAA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
111 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.532+2428_532+2429d others(4): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112178257 | ||||||
| chr2:112178265 | A | C | 1 | a0001c0001t0001g0227 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.532+2426A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178265 | |||||||
| chr2:112178269 | C | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
254 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.532+2430C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178269 | |||||||
| chr2:112178274 | A | G | 45 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0036 others(42): Show |
51 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.532+2435A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178274 | |||||||
| chr2:112178327 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0050 |
3 | HG01346.hp2 HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.532+2488C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178327 | |||||||
| chr2:112178373 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.532+2534C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178373 | |||||||
| chr2:112178512 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.532+2673G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178512 | |||||||
| chr2:112178583 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.532+2744C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178583 | |||||||
| chr2:112178685 | A | C | 14 | a0001c0001t0001g0038 a0001c0001t0001g0058 a0001c0001t0001g0059 others(11): Show |
14 | HG01167.hp1 HG01243.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.532+2846A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178685 | |||||||
| chr2:112178799 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.533-2940A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178799 | |||||||
| chr2:112178904 | G | GGCAAAAG others(6): Show |
220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
254 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.533-2832_533-2831i others(15): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112178904 | ||||||
| chr2:112179084 | A | C | 1 | a0001c0001t0001g0167 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.533-2655A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179084 | |||||||
| chr2:112179425 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.533-2314C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179425 | |||||||
| chr2:112179488 | ATTACT | A | 6 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0243 others(3): Show |
6 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.533-2247_533-2243d others(7): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112179488 | ||||||
| chr2:112179569 | A | G | 1 | a0001c0001t0012g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.533-2170A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179569 | |||||||
| chr2:112179647 | G | A | 1 | a0001c0001t0005g0240 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.533-2092G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179647 | |||||||
| chr2:112179661 | C | T | 1 | a0002c0002t0002g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.533-2078C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179661 | |||||||
| chr2:112179709 | C | A | 1 | a0008c0010t0001g0263 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.533-2030C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179709 | |||||||
| chr2:112179729 | A | G | 1 | a0002c0002t0002g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.533-2010A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179729 | |||||||
| chr2:112179890 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.533-1849G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179890 | |||||||
| chr2:112179893 | G | A | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
66 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.533-1846G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179893 | |||||||
| chr2:112180120 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.533-1619A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180120 | |||||||
| chr2:112180174 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.533-1565C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180174 | |||||||
| chr2:112180187 | A | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0246 others(4): Show |
8 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.533-1552A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180187 | |||||||
| chr2:112180387 | G | C | 16 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0039 others(13): Show |
18 | HG00639.hp2 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.533-1352G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180387 | |||||||
| chr2:112180432 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.533-1307G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180432 | |||||||
| chr2:112180534 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.533-1205C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180534 | |||||||
| chr2:112180562 | G | C | 1 | a0001c0001t0001g0227 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.533-1177G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180562 | |||||||
| chr2:112180646 | C | T | 3 | a0001c0001t0002g0139 a0001c0001t0002g0239 a0001c0001t0013g0289 |
3 | HG03225.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.533-1093C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180646 | |||||||
| chr2:112180649 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.533-1090G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180649 | |||||||
| chr2:112180731 | T | C | 1 | a0001c0001t0006g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.533-1008T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180731 | |||||||
| chr2:112180763 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.533-976A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180763 | |||||||
| chr2:112180774 | T | A | 9 | a0001c0001t0002g0174 a0001c0001t0004g0018 a0001c0001t0004g0019 others(6): Show |
11 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(8): Show |
intron_variant | MODIFIER | c.533-965T>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180774 | |||||||
| chr2:112180795 | C | T | 3 | a0001c0001t0001g0238 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG01074.hp2 HG01081.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.533-944C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180795 | |||||||
| chr2:112180871 | G | A | 1 | a0001c0001t0005g0282 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.533-868G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180871 | |||||||
| chr2:112180877 | C | T | 1 | a0001c0001t0005g0288 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.533-862C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180877 | |||||||
| chr2:112180892 | CAGCCTGG others(34): Show |
C | 4 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0243 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.533-845_533-805del others(41): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112180892 | ||||||
| chr2:112180901 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.533-838C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180901 | |||||||
| chr2:112180902 | G | A | 2 | a0001c0001t0003g0067 a0001c0001t0003g0086 |
2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.533-837G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180902 | |||||||
| chr2:112180922 | C | CA | 14 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(11): Show |
14 | HG00642.hp2 HG01884.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.533-794dupA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112180922 | ||||||
| chr2:112180922 | CA | C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(60): Show |
69 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.533-794delA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112180922 | ||||||
| chr2:112180922 | CAA | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(24): Show |
28 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.533-795_533-794del others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112180922 | ||||||
| chr2:112180922 | CAAA | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.533-796_533-794del others(3): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112180922 | ||||||
| chr2:112180998 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.533-741C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180998 | |||||||
| chr2:112181040 | A | G | 9 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0140 others(6): Show |
9 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.533-699A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181040 | |||||||
| chr2:112181131 | T | C | 1 | a0001c0001t0005g0282 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.533-608T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181131 | |||||||
| chr2:112181138 | C | T | 44 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0037 others(41): Show |
50 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.533-601C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181138 | |||||||
| chr2:112181159 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.533-580G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181159 | |||||||
| chr2:112181288 | A | C | 1 | a0002c0002t0002g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.533-451A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181288 | |||||||
| chr2:112181415 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.533-324G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181415 | |||||||
| chr2:112181465 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.533-274C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181465 | |||||||
| chr2:112181538 | T | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
254 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.533-201T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181538 | |||||||
| chr2:112181626 | C | T | 50 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
60 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.533-113C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181626 | |||||||
| chr2:112181632 | G | A | 24 | a0001c0001t0001g0037 a0001c0001t0001g0238 a0001c0001t0001g0253 others(21): Show |
28 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.533-107G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181632 | |||||||
| chr2:112181680 | A | C | 1 | a0001c0001t0004g0132 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.533-59A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181680 | |||||||
| chr2:112181971 | T | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(65): Show |
79 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.670+95T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | chr2 | 112181971 | |||||||
| chr2:112182034 | G | C | 1 | a0001c0001t0006g0126 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.670+158G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | chr2 | 112182034 | |||||||
| chr2:112182315 | A | G | 1 | a0001c0001t0005g0240 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.670+439A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | chr2 | 112182315 | |||||||
| chr2:112182422 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.671-369A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | chr2 | 112182422 | |||||||
| chr2:112182483 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0267 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.671-308G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | chr2 | 112182483 | |||||||
| chr2:112182566 | ACTC | A | 68 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(65): Show |
79 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.671-219_671-217del others(3): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 112182566 | ||||||
| chr2:112182594 | G | A | 66 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
76 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.671-197G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | chr2 | 112182594 | |||||||
| chr2:112182729 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.671-62G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | chr2 | 112182729 | |||||||
| chr2:112183001 | C | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(64): Show |
78 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.808+73C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183001 | |||||||
| chr2:112183152 | C | T | 1 | a0001c0001t0008g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.808+224C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183152 | |||||||
| chr2:112183215 | A | G | 8 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0140 others(5): Show |
8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.808+287A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183215 | |||||||
| chr2:112183216 | C | T | 1 | a0001c0001t0005g0282 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.808+288C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183216 | |||||||
| chr2:112183409 | A | G | 1 | a0001c0001t0005g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.808+481A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183409 | |||||||
| chr2:112183507 | T | A | 41 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0037 others(38): Show |
47 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.808+579T>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183507 | |||||||
| chr2:112183610 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.808+682C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183610 | |||||||
| chr2:112183696 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0050 |
3 | HG01346.hp2 HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.808+768C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183696 | |||||||
| chr2:112183795 | A | G | 47 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0037 others(44): Show |
53 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.808+867A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183795 | |||||||
| chr2:112183807 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.808+879A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183807 | |||||||
| chr2:112184073 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
258 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.809-1128T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184073 | |||||||
| chr2:112184074 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.809-1127G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184074 | |||||||
| chr2:112184082 | C | G | 1 | a0001c0001t0005g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.809-1119C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184082 | |||||||
| chr2:112184107 | A | G | 6 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0243 others(3): Show |
6 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-1094A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184107 | |||||||
| chr2:112184146 | G | A | 5 | a0001c0001t0001g0154 a0001c0001t0001g0162 a0001c0001t0001g0220 others(2): Show |
5 | HG01167.hp1 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-1055G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184146 | |||||||
| chr2:112184245 | T | C | 6 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0243 others(3): Show |
6 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-956T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184245 | |||||||
| chr2:112184272 | C | T | 6 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0243 others(3): Show |
6 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-929C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184272 | |||||||
| chr2:112184353 | T | C | 11 | a0001c0001t0001g0146 a0001c0001t0003g0031 a0001c0001t0003g0032 others(8): Show |
11 | HG02451.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.809-848T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184353 | |||||||
| chr2:112184363 | G | A | 40 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0037 others(37): Show |
46 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.809-838G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184363 | |||||||
| chr2:112184455 | C | T | 1 | a0002c0002t0002g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.809-746C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184455 | |||||||
| chr2:112184576 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.809-625C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184576 | |||||||
| chr2:112184685 | G | A | 1 | a0010c0013t0001g0221 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.809-516G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184685 | |||||||
| chr2:112184685 | G | GTATATAT others(95): Show |
1 | a0001c0001t0001g0167 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.809-458_809-457ins others(102): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 112184685 | ||||||
| chr2:112184685 | G | GTATATAT others(19): Show |
1 | a0001c0001t0001g0080 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.809-497_809-496ins others(26): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 112184685 | ||||||
| chr2:112184685 | G | GTATATAT others(21): Show |
151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
173 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.809-497_809-496ins others(28): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 112184685 | ||||||
| chr2:112184722 | T | C | 5 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0243 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.809-479T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184722 | |||||||
| chr2:112184734 | G | T | 1 | a0001c0001t0001g0281 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.809-467G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184734 | |||||||
| chr2:112184745 | T | C | 5 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0243 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.809-456T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184745 | |||||||
| chr2:112184807 | CAT | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
170 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.809-382_809-381del others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 112184807 | ||||||
| chr2:112184836 | T | TAC | 6 | a0001c0001t0001g0235 a0001c0001t0005g0033 a0001c0001t0005g0062 others(3): Show |
6 | HG01109.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-355_809-354dup others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 112184836 | ||||||
| chr2:112184846 | C | CAT | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0037 others(32): Show |
41 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.809-344_809-343dup others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 112184846 | ||||||
| chr2:112184869 | A | G | 1 | a0002c0002t0003g0064 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.809-332A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184869 | |||||||
| chr2:112185493 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
280 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.947+154C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112185493 | |||||||
| chr2:112185698 | G | A | 1 | a0001c0001t0005g0136 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.947+359G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112185698 | |||||||
| chr2:112185868 | CT | C | 6 | a0001c0001t0001g0150 a0001c0001t0001g0191 a0001c0001t0001g0268 others(3): Show |
6 | HG00140.hp1 HG01516.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.947+545delT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 112185868 | ||||||
| chr2:112185961 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.947+622T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112185961 | |||||||
| chr2:112186006 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
281 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.947+667G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186006 | |||||||
| chr2:112186136 | C | G | 5 | a0001c0001t0001g0165 a0001c0001t0001g0170 a0001c0001t0001g0177 others(2): Show |
5 | NA18960.hp1 NA18962.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.947+797C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186136 | |||||||
| chr2:112186295 | A | G | 46 | a0001c0001t0001g0147 a0001c0001t0002g0012 a0001c0001t0002g0017 others(43): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.948-839A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186295 | |||||||
| chr2:112186339 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0164 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.948-795C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186339 | |||||||
| chr2:112186340 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.948-794G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186340 | |||||||
| chr2:112186404 | C | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
5 | HG03239.hp1 HG03688.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.948-730C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186404 | |||||||
| chr2:112186414 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0001g0235 |
3 | HG02970.hp1 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.948-720C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186414 | |||||||
| chr2:112186446 | C | G | 1 | a0001c0001t0005g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.948-688C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186446 | |||||||
| chr2:112186468 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0005g0282 |
2 | HG00673.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.948-666C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186468 | |||||||
| chr2:112186519 | A | G | 1 | a0001c0005t0007g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.948-615A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186519 | |||||||
| chr2:112186747 | A | G | 4 | a0001c0001t0001g0071 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
4 | HG00741.hp2 HG01981.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.948-387A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186747 |