Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26127 |
| ensemblid | ENSG00000111790.14 |
| hgncid | 23098 |
| symbol | FGFR1OP2 |
| name | FGFR1 oncogene partner 2 |
| refseq_nuc | NM_015633.3 |
| refseq_prot | NP_056448.1 |
| ensembl_nuc | ENST00000229395.8 |
| ensembl_prot | ENSP00000229395.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 26938470 |
| end | 26966648 |
| strand | + |
| ver | v1.2 |
| region | chr12:26938470-26966648 |
| region5000 | chr12:26933470-26971648 |
| regionname0 | FGFR1OP2_chr12_26938470_26966648 |
| regionname5000 | FGFR1OP2_chr12_26933470_26971648 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 253 | 420 | 79 | 76 | 203 | 18 | 42 | 162 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | MSCTI others(248): Show |
chr12 | 26933470 | 26971648 |
| a0002 | 0/0 | 253 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | MSCTI others(248): Show |
chr12 | 26933470 | 26971648 |
| a0003 | 0/0 | 253 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | MSCTI others(248): Show |
chr12 | 26933470 | 26971648 |
| a0004 | 0/0 | 253 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | MSCTI others(248): Show |
chr12 | 26933470 | 26971648 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 759 | 420 | 79 | 76 | 203 | 18 | 42 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | ATGAG others(754): Show |
chr12 | 26933470 | 26971648 | ||
| a0002c0002 | 0/0 | 759 | 4 | 0 | 0 | 4 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | ATGAG others(754): Show |
chr12 | 26933470 | 26971648 | ||
| a0003c0004 | 0/0 | 759 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | ATGAG others(754): Show |
chr12 | 26933470 | 26971648 | ||
| a0004c0003 | 0/0 | 759 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | ATGAG others(754): Show |
chr12 | 26933470 | 26971648 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2932 | 128 | 26 | 12 | 72 | 5 | 13 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2927): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0002 | 0/1 | 2933 | 88 | 4 | 32 | 37 | 4 | 10 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0003 | 0/0 | 2932 | 59 | 5 | 1 | 47 | 1 | 5 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2927): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0004 | 0/0 | 2933 | 53 | 3 | 12 | 32 | 3 | 3 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0005 | 0/0 | 2934 | 37 | 7 | 9 | 9 | 4 | 8 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2929): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0006 | 1/0 | 2932 | 14 | 5 | 5 | 2 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2927): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0007 | 0/0 | 2932 | 9 | 9 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2927): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0008 | 0/0 | 2933 | 4 | 2 | 2 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0009 | 0/0 | 2932 | 4 | 4 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2927): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0010 | 0/0 | 2933 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0011 | 0/0 | 2933 | 3 | 0 | 2 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0012 | 0/0 | 2932 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2927): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0013 | 0/0 | 2934 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2929): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0014 | 0/0 | 2933 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0015 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2927): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0016 | 0/0 | 2934 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2929): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0017 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2927): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0018 | 0/0 | 2933 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0019 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2927): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0020 | 0/0 | 2933 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0021 | 0/0 | 2933 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0022 | 0/0 | 2932 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2927): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0023 | 0/0 | 2933 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0024 | 0/0 | 2934 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2929): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0025 | 0/0 | 2933 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0026 | 0/0 | 2933 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0027 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2927): Show |
chr12 | 26933470 | 26971648 |
| a0001c0001t0028 | 0/0 | 2942 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2937): Show |
chr12 | 26933470 | 26971648 |
| a0002c0002t0002 | 0/0 | 2933 | 4 | 0 | 0 | 4 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| a0003c0004t0002 | 0/0 | 2933 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| a0004c0003t0008 | 0/0 | 2933 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | AGTTC others(2928): Show |
chr12 | 26933470 | 26971648 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0004 | 0/0 | 8 | 6 | 1 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0007 | 0/0 | 5 | 1 | 1 | 1 | 2 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0016 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0001 | 0/0 | 13 | 0 | 6 | 6 | 1 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0002 | 0/0 | 10 | 0 | 1 | 7 | 0 | 2 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0044 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0015 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0021 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0006g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0006g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0006g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0006g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0006g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0006g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0006g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0007g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0007g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0008g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0008g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0009g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0009g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0010g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0010g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0010g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0011g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0011g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0012g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0013g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0014g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0015g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0016g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0017g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0018g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0019g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0020g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0021g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0022g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0023g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0024g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0025g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0026g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0027g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0001c0001t0028g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0002c0002t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0003c0004t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| a0004c0003t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0069 | EUR | GBR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0015 | EUR | GBR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | GBR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0104 | EUR | FIN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0187 | EUR | FIN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | CHS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0228 | EAS | CHS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00673 | hp2 | a0001 | c0001 | t0023 | g0049 | EAS | CHS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0181 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0280 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0101 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0175 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0048 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0176 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0188 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01109 | hp1 | a0001 | c0001 | t0011 | g0222 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0252 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0195 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0249 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01243 | hp1 | a0001 | c0001 | t0021 | g0001 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0282 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01358 | hp1 | a0001 | c0001 | t0011 | g0002 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0105 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0220 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0191 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0044 | EUR | IBS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0167 | EUR | IBS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0021 | EUR | IBS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0183 | EUR | IBS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0044 | EUR | IBS | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0286 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0287 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0048 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0204 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0046 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0201 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0039 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0178 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0289 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02135 | hp1 | a0003 | c0004 | t0002 | g0096 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | ACB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0288 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CDX | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CDX | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CDX | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0043 | AFR | ACB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0100 | AFR | ACB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0184 | AFR | ACB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0285 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0103 | AFR | ACB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0213 | EAS | KHV | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0054 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0055 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02630 | hp2 | a0001 | c0001 | t0013 | g0171 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0015 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0080 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0277 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0132 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0055 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0278 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02886 | hp2 | a0001 | c0001 | t0014 | g0062 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0283 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0284 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02922 | hp1 | a0001 | c0001 | t0018 | g0086 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0182 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0202 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0134 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0214 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03139 | hp1 | a0001 | c0001 | t0012 | g0043 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03139 | hp2 | a0001 | c0001 | t0025 | g0290 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | MSL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03209 | hp2 | a0001 | c0001 | t0027 | g0137 | AFR | MSL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03225 | hp1 | a0001 | c0001 | t0015 | g0007 | AFR | MSL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0215 | AFR | MSL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0190 | AFR | MSL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0133 | AFR | MSL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0281 | AFR | MSL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0054 | AFR | MSL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03540 | hp2 | a0001 | c0001 | t0017 | g0125 | AFR | GWD | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0247 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | STU | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0208 | SAS | STU | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03704 | hp1 | a0001 | c0001 | t0022 | g0059 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0174 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0179 | SAS | PJL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03831 | hp2 | a0001 | c0001 | t0026 | g0005 | SAS | BEB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0203 | SAS | BEB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | STU | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | STU | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | BEB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0177 | SAS | STU | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0194 | SAS | STU | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0246 | SAS | STU | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | STU | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | STU | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0186 | SAS | STU | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0251 | AFR | YRI | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | YRI | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18962 | hp1 | a0001 | c0001 | t0024 | g0212 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18972 | hp2 | a0001 | c0001 | t0011 | g0129 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0227 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0226 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18985 | hp1 | a0001 | c0001 | t0006 | g0047 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18997 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19030 | hp2 | a0004 | c0003 | t0008 | g0192 | AFR | LWK | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | LWK | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | LWK | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0230 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19060 | hp2 | a0001 | c0001 | t0020 | g0098 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19076 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19076 | hp2 | a0001 | c0001 | t0005 | g0229 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | YRI | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | YRI | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ASW | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ASW | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA20752 | hp2 | a0001 | c0001 | t0028 | g0276 | EUR | TSI | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0189 | EUR | TSI | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0051 | EUR | TSI | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0102 | SAS | GIH | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0077 | SAS | GIH | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0193 | AMR | CLM | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0279 | AFR | ACB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0196 | AFR | ACB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0099 | AFR | ACB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0185 | AFR | MSL | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | USA | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0250 | AFR | USA | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | USA | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | USA | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | LWK | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| NA21309 | hp2 | a0001 | c0001 | t0019 | g0006 | AFR | LWK | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0155 | REF | REF | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0154 | REF | REF | FGFR1OP2_chr12_26933470_26971648 | FGFR1OP2 | chr12 | 26933470 | 26971648 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:26954228 | G | A | 1 | a0004 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.70G>A | p.Asp24Asn | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/7 | 325/2932 | 70/762 | 24/253 | chr12 | 26954228 | |||
| chr12:26956607 | T | C | 1 | a0003 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.200T>C | p.Met67Thr | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/7 | 455/2932 | 200/762 | 67/253 | chr12 | 26956607 | |||
| chr12:26964729 | G | A | 1 | a0002 | 4 | NA18942.hp1 NA18986.hp1 NA18990.hp1 others(1): Show |
missense_variant | MODERATE | c.758G>A | p.Ser253Asn | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 1013/2932 | 758/762 | 253/253 | chr12 | 26964729 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:26938493 | A | AGGCGGTC others(3): Show |
1 | a0001c0001t0028 | 1 | NA20752.hp2 | 5_prime_UTR_variant | MODIFIER | c.-229_-220dupCGGTCG others(4): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/7 | 15653 | INFO_REALIGN_3_PRIME | chr12 | 26938493 | |||||
| chr12:26938522 | G | A | 6 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0014 others(3): Show |
9 | HG01167.hp1 HG01192.hp1 HG02280.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-203G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/7 | 15637 | chr12 | 26938522 | ||||||
| chr12:26938524 | T | G | 6 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0014 others(3): Show |
9 | HG01167.hp1 HG01192.hp1 HG02280.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-201T>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/7 | 15635 | chr12 | 26938524 | ||||||
| chr12:26938611 | G | A | 1 | a0001c0001t0017 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-114G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/7 | 15548 | chr12 | 26938611 | ||||||
| chr12:26964757 | C | T | 1 | a0001c0001t0027 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*24C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 24 | chr12 | 26964757 | ||||||
| chr12:26965555 | T | C | 1 | a0001c0001t0010 | 3 | HG02723.hp1 HG03041.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*822T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 822 | chr12 | 26965555 | ||||||
| chr12:26965680 | C | A | 21 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(18): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
3_prime_UTR_variant | MODIFIER | c.*947C>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 947 | chr12 | 26965680 | ||||||
| chr12:26965700 | C | T | 1 | a0001c0001t0021 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*967C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 967 | chr12 | 26965700 | ||||||
| chr12:26965726 | TC | T | 1 | a0001c0001t0007 | 9 | HG02451.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*995delC | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 995 | INFO_REALIGN_3_PRIME | chr12 | 26965726 | |||||
| chr12:26965775 | G | A | 1 | a0001c0001t0012 | 2 | HG02257.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1042G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 1042 | chr12 | 26965775 | ||||||
| chr12:26965849 | T | A | 1 | a0001c0001t0022 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1116T>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 1116 | chr12 | 26965849 | ||||||
| chr12:26965911 | G | A | 2 | a0001c0001t0013 a0001c0001t0018 |
2 | HG02630.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1178G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 1178 | chr12 | 26965911 | ||||||
| chr12:26965920 | G | A | 1 | a0001c0001t0023 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1187G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 1187 | chr12 | 26965920 | ||||||
| chr12:26965999 | T | G | 1 | a0001c0001t0019 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1266T>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 1266 | chr12 | 26965999 | ||||||
| chr12:26966215 | C | T | 1 | a0001c0001t0020 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1482C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 1482 | chr12 | 26966215 | ||||||
| chr12:26966332 | A | G | 1 | a0001c0001t0026 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1599A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 1599 | chr12 | 26966332 | ||||||
| chr12:26966451 | C | G | 1 | a0001c0001t0025 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1718C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 1718 | chr12 | 26966451 | ||||||
| chr12:26966541 | A | AT | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(11): Show |
168 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1824dupT | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 1825 | INFO_REALIGN_3_PRIME | chr12 | 26966541 | |||||
| chr12:26966541 | A | ATT | 4 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0016 others(1): Show |
40 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1823_*1824dupTT | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 1825 | INFO_REALIGN_3_PRIME | chr12 | 26966541 | |||||
| chr12:26966542 | T | TG | 2 | a0001c0001t0011 a0001c0001t0014 |
4 | HG01109.hp1 HG01358.hp1 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1809_*1810insG | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 1810 | chr12 | 26966542 | ||||||
| chr12:26966543 | T | G | 1 | a0001c0001t0003 | 59 | HG00099.hp2 HG00642.hp1 HG02071.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1810T>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 1810 | chr12 | 26966543 | ||||||
| chr12:26966569 | A | C | 1 | a0001c0001t0009 | 4 | HG02572.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1836A>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 7/7 | 1836 | chr12 | 26966569 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:26938795 | T | G | 1 | a0001c0001t0001g0058 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-15+85T>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26938795 | |||||||
| chr12:26939099 | A | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0291 |
3 | HG00558.hp2 NA18973.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.-15+389A>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26939099 | |||||||
| chr12:26939119 | C | T | 1 | a0001c0001t0025g0290 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+409C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26939119 | |||||||
| chr12:26939193 | A | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(60): Show |
88 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.-15+483A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26939193 | |||||||
| chr12:26939246 | T | C | 1 | a0001c0001t0025g0290 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+536T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26939246 | |||||||
| chr12:26939258 | G | A | 1 | a0001c0001t0022g0059 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-15+548G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26939258 | |||||||
| chr12:26939282 | G | C | 1 | a0001c0001t0001g0238 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-15+572G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26939282 | |||||||
| chr12:26939316 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
4 | NA19011.hp2 NA19056.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+606T>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26939316 | |||||||
| chr12:26939434 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-15+724G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26939434 | |||||||
| chr12:26939484 | A | G | 16 | a0001c0001t0001g0052 a0001c0001t0001g0231 a0001c0001t0001g0232 others(13): Show |
17 | HG00597.hp2 HG02056.hp2 NA18939.hp2 others(14): Show |
intron_variant | MODIFIER | c.-15+774A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26939484 | |||||||
| chr12:26939853 | A | G | 1 | a0001c0001t0011g0222 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-15+1143A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26939853 | |||||||
| chr12:26939864 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-15+1154G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26939864 | |||||||
| chr12:26939938 | G | A | 2 | a0001c0001t0003g0063 a0001c0001t0014g0062 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-15+1228G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26939938 | |||||||
| chr12:26940038 | A | G | 89 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0173 others(86): Show |
110 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.-15+1328A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26940038 | |||||||
| chr12:26940177 | G | A | 34 | a0001c0001t0001g0066 a0001c0001t0002g0083 a0001c0001t0003g0002 others(31): Show |
53 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.-15+1467G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26940177 | |||||||
| chr12:26940283 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-15+1573G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26940283 | |||||||
| chr12:26940373 | A | C | 1 | a0001c0001t0002g0172 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-15+1663A>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26940373 | |||||||
| chr12:26940488 | T | A | 1 | a0001c0001t0001g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-15+1778T>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26940488 | |||||||
| chr12:26940545 | G | T | 1 | a0001c0001t0028g0276 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-15+1835G>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26940545 | |||||||
| chr12:26940603 | A | G | 2 | a0001c0001t0012g0043 a0001c0001t0013g0171 |
3 | HG02257.hp1 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-15+1893A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26940603 | |||||||
| chr12:26940627 | A | C | 1 | a0001c0001t0002g0170 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-15+1917A>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26940627 | |||||||
| chr12:26940652 | G | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(261): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.-15+1942G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26940652 | |||||||
| chr12:26940874 | CTATTTAT others(34): Show |
C | 1 | a0001c0001t0001g0270 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-15+2166_-15+2206d others(43): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26940874 | ||||||
| chr12:26941099 | A | G | 1 | a0001c0001t0005g0220 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-15+2389A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26941099 | |||||||
| chr12:26941100 | T | A | 2 | a0001c0001t0002g0221 a0001c0001t0018g0086 |
2 | HG02895.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-15+2390T>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26941100 | |||||||
| chr12:26941200 | C | G | 1 | a0001c0001t0002g0148 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-15+2490C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26941200 | |||||||
| chr12:26941456 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-15+2746G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26941456 | |||||||
| chr12:26941803 | T | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
7 | NA18940.hp2 NA18961.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+3093T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26941803 | |||||||
| chr12:26941946 | T | C | 11 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0090 others(8): Show |
13 | HG02027.hp2 HG02135.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+3236T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26941946 | |||||||
| chr12:26941966 | C | T | 1 | a0001c0001t0003g0063 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-15+3256C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26941966 | |||||||
| chr12:26941994 | G | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0002g0217 |
3 | HG02257.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-15+3284G>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26941994 | |||||||
| chr12:26942026 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-15+3316G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26942026 | |||||||
| chr12:26942182 | G | A | 1 | a0001c0001t0012g0043 | 2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-15+3472G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26942182 | |||||||
| chr12:26942530 | A | G | 1 | a0001c0001t0002g0042 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-15+3820A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26942530 | |||||||
| chr12:26942649 | A | C | 1 | a0001c0001t0003g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-15+3939A>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26942649 | |||||||
| chr12:26942685 | G | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-15+3975G>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26942685 | |||||||
| chr12:26942778 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-15+4068T>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26942778 | |||||||
| chr12:26942858 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-15+4148A>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26942858 | |||||||
| chr12:26942859 | G | A | 1 | a0001c0001t0002g0244 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-15+4149G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26942859 | |||||||
| chr12:26942960 | TTA | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0002g0217 |
3 | HG02257.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-15+4252_-15+4253d others(4): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26942960 | ||||||
| chr12:26943165 | A | G | 2 | a0001c0001t0006g0214 a0001c0001t0006g0215 |
2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-15+4455A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26943165 | |||||||
| chr12:26943275 | T | TAA | 33 | a0001c0001t0001g0173 a0001c0001t0001g0216 a0001c0001t0001g0245 others(30): Show |
40 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.-15+4567_-15+4568d others(4): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26943275 | ||||||
| chr12:26943300 | C | G | 36 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0002g0032 others(33): Show |
38 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15+4590C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26943300 | |||||||
| chr12:26943403 | T | C | 1 | a0001c0001t0003g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-15+4693T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26943403 | |||||||
| chr12:26943470 | TA | T | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.-15+4767delA | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26943470 | ||||||
| chr12:26943574 | C | A | 23 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0002g0217 others(20): Show |
24 | HG00738.hp1 HG01123.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.-15+4864C>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26943574 | |||||||
| chr12:26943647 | A | C | 1 | a0001c0001t0011g0222 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-15+4937A>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26943647 | |||||||
| chr12:26943654 | A | G | 2 | a0001c0001t0003g0248 a0001c0001t0027g0137 |
2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-15+4944A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26943654 | |||||||
| chr12:26943663 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-15+4953A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26943663 | |||||||
| chr12:26943685 | C | T | 1 | a0001c0001t0005g0102 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-15+4975C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26943685 | |||||||
| chr12:26943694 | G | A | 2 | a0001c0001t0002g0149 a0001c0001t0005g0225 |
2 | HG04115.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-15+4984G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26943694 | |||||||
| chr12:26943697 | C | T | 1 | a0001c0001t0027g0137 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-15+4987C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26943697 | |||||||
| chr12:26943739 | C | G | 1 | a0001c0001t0002g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-15+5029C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26943739 | |||||||
| chr12:26944067 | A | G | 1 | a0001c0001t0003g0082 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-15+5357A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26944067 | |||||||
| chr12:26944198 | A | T | 1 | a0001c0001t0005g0190 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-15+5488A>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26944198 | |||||||
| chr12:26944557 | A | G | 1 | a0001c0001t0002g0135 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-15+5847A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26944557 | |||||||
| chr12:26944571 | G | T | 1 | a0001c0001t0003g0081 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-15+5861G>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26944571 | |||||||
| chr12:26944579 | A | G | 66 | a0001c0001t0001g0051 a0001c0001t0001g0218 a0001c0001t0001g0219 others(63): Show |
81 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-15+5869A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26944579 | |||||||
| chr12:26944765 | G | C | 2 | a0001c0001t0004g0044 a0001c0001t0004g0189 |
3 | HG01515.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-15+6055G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26944765 | |||||||
| chr12:26944794 | T | C | 4 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0064 others(1): Show |
9 | NA18943.hp1 NA18967.hp2 NA18979.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+6084T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26944794 | |||||||
| chr12:26944994 | T | A | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0039 others(23): Show |
28 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-15+6284T>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26944994 | |||||||
| chr12:26945214 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-15+6504C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945214 | |||||||
| chr12:26945269 | T | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
222 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.-15+6559T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945269 | |||||||
| chr12:26945405 | G | C | 1 | a0001c0001t0002g0221 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-15+6695G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945405 | |||||||
| chr12:26945494 | C | A | 6 | a0001c0001t0005g0225 a0001c0001t0005g0226 a0001c0001t0005g0227 others(3): Show |
6 | HG00597.hp2 NA18974.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+6784C>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945494 | |||||||
| chr12:26945541 | G | C | 1 | a0001c0001t0001g0253 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-15+6831G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945541 | |||||||
| chr12:26945598 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-15+6888C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945598 | |||||||
| chr12:26945655 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0035 others(5): Show |
13 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+6945G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945655 | |||||||
| chr12:26945717 | C | T | 3 | a0001c0001t0010g0132 a0001c0001t0010g0133 a0001c0001t0010g0134 |
3 | HG02723.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-15+7007C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945717 | |||||||
| chr12:26945856 | C | T | 3 | a0001c0001t0010g0132 a0001c0001t0010g0133 a0001c0001t0010g0134 |
3 | HG02723.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-15+7146C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945856 | |||||||
| chr12:26945857 | G | A | 33 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0017 others(30): Show |
52 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.-15+7147G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945857 | |||||||
| chr12:26945861 | C | CA | 10 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0088 others(7): Show |
11 | HG01109.hp2 HG01175.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15+7169dupA | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26945861 | ||||||
| chr12:26945861 | CA | C | 30 | a0001c0001t0001g0130 a0001c0001t0001g0216 a0001c0001t0001g0267 others(27): Show |
35 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.-15+7169delA | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26945861 | ||||||
| chr12:26945862 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-15+7152A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945862 | |||||||
| chr12:26945863 | A | G | 27 | a0001c0001t0001g0216 a0001c0001t0005g0015 a0001c0001t0005g0021 others(24): Show |
32 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.-15+7153A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945863 | |||||||
| chr12:26945889 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(84): Show |
139 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-15+7179G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945889 | |||||||
| chr12:26945967 | G | T | 39 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0002g0032 others(36): Show |
41 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.-15+7257G>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945967 | |||||||
| chr12:26945994 | G | A | 2 | a0001c0001t0013g0171 a0001c0001t0018g0086 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-15+7284G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26945994 | |||||||
| chr12:26946001 | GTT | G | 3 | a0001c0001t0007g0009 a0001c0001t0007g0019 a0001c0001t0007g0103 |
9 | HG02451.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+7292_-15+7293d others(4): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26946001 | |||||||
| chr12:26946350 | G | C | 29 | a0001c0001t0001g0173 a0001c0001t0001g0216 a0001c0001t0005g0015 others(26): Show |
35 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.-15+7640G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26946350 | |||||||
| chr12:26946446 | G | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0255 |
2 | HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-14-7699G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26946446 | |||||||
| chr12:26946555 | C | G | 1 | a0001c0001t0027g0137 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-14-7590C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26946555 | |||||||
| chr12:26946604 | G | A | 1 | a0001c0001t0005g0174 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-14-7541G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26946604 | |||||||
| chr12:26946669 | G | C | 1 | a0001c0001t0002g0152 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-14-7476G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26946669 | |||||||
| chr12:26946744 | G | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(126): Show |
195 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.-14-7401G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26946744 | |||||||
| chr12:26946782 | C | A | 36 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0002g0032 others(33): Show |
38 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.-14-7363C>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26946782 | |||||||
| chr12:26946786 | G | A | 36 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0017 others(33): Show |
55 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.-14-7359G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26946786 | |||||||
| chr12:26946850 | C | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0002g0217 |
3 | HG02257.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-14-7295C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26946850 | |||||||
| chr12:26947002 | G | A | 2 | a0001c0001t0005g0175 a0001c0001t0005g0176 |
2 | HG01070.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.-14-7143G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26947002 | |||||||
| chr12:26947010 | C | A | 3 | a0001c0001t0010g0132 a0001c0001t0010g0133 a0001c0001t0010g0134 |
3 | HG02723.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-14-7135C>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26947010 | |||||||
| chr12:26947061 | A | T | 1 | a0001c0001t0018g0086 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-7084A>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26947061 | |||||||
| chr12:26947068 | C | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0002g0217 |
3 | HG02257.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-14-7077C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26947068 | |||||||
| chr12:26947091 | C | T | 28 | a0001c0001t0001g0173 a0001c0001t0001g0216 a0001c0001t0005g0015 others(25): Show |
33 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-14-7054C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26947091 | |||||||
| chr12:26947349 | A | G | 1 | a0001c0001t0002g0151 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-14-6796A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26947349 | |||||||
| chr12:26947390 | G | A | 1 | a0001c0001t0006g0191 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-14-6755G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26947390 | |||||||
| chr12:26947493 | G | A | 1 | a0001c0001t0027g0137 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-14-6652G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26947493 | |||||||
| chr12:26947559 | T | A | 22 | a0001c0001t0004g0045 a0001c0001t0004g0105 a0001c0001t0004g0281 others(19): Show |
23 | HG00738.hp1 HG01123.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.-14-6586T>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26947559 | |||||||
| chr12:26947628 | G | A | 1 | a0001c0001t0002g0153 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-14-6517G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26947628 | |||||||
| chr12:26947677 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-14-6468C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26947677 | |||||||
| chr12:26947922 | G | A | 1 | a0001c0001t0002g0090 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-14-6223G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26947922 | |||||||
| chr12:26947931 | A | G | 40 | a0001c0001t0001g0198 a0001c0001t0003g0002 a0001c0001t0003g0008 others(37): Show |
61 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.-14-6214A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26947931 | |||||||
| chr12:26947959 | A | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-14-6186A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26947959 | |||||||
| chr12:26948111 | C | G | 28 | a0001c0001t0001g0173 a0001c0001t0001g0216 a0001c0001t0005g0015 others(25): Show |
33 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-14-6034C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26948111 | |||||||
| chr12:26948176 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-14-5969T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26948176 | |||||||
| chr12:26948196 | T | C | 1 | a0001c0001t0005g0246 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-14-5949T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26948196 | |||||||
| chr12:26948250 | G | A | 28 | a0001c0001t0001g0173 a0001c0001t0001g0216 a0001c0001t0005g0015 others(25): Show |
33 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-14-5895G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26948250 | |||||||
| chr12:26948347 | G | A | 2 | a0001c0001t0005g0174 a0001c0001t0005g0177 |
2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-14-5798G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26948347 | |||||||
| chr12:26948709 | C | T | 36 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0002g0032 others(33): Show |
38 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.-14-5436C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26948709 | |||||||
| chr12:26948786 | G | C | 1 | a0001c0001t0004g0200 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-14-5359G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26948786 | |||||||
| chr12:26949098 | G | T | 1 | a0001c0001t0002g0126 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-14-5047G>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26949098 | |||||||
| chr12:26949191 | A | C | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0039 others(23): Show |
28 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14-4954A>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26949191 | |||||||
| chr12:26949198 | C | T | 1 | a0001c0001t0002g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-14-4947C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26949198 | |||||||
| chr12:26949221 | C | T | 36 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0002g0032 others(33): Show |
38 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.-14-4924C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26949221 | |||||||
| chr12:26949231 | G | A | 4 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 others(1): Show |
4 | NA18968.hp2 NA18989.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-4914G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26949231 | |||||||
| chr12:26949239 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(119): Show |
186 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.-14-4906G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26949239 | |||||||
| chr12:26949424 | A | T | 2 | a0001c0001t0003g0079 a0001c0001t0003g0080 |
2 | HG02698.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-14-4721A>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26949424 | |||||||
| chr12:26949653 | G | A | 261 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(258): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-14-4492G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26949653 | |||||||
| chr12:26949703 | C | T | 1 | a0001c0001t0025g0290 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14-4442C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26949703 | |||||||
| chr12:26949732 | C | G | 30 | a0001c0001t0001g0060 a0001c0001t0002g0001 a0001c0001t0002g0010 others(27): Show |
50 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.-14-4413C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26949732 | |||||||
| chr12:26949924 | A | G | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(289): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.-14-4221A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26949924 | |||||||
| chr12:26950017 | G | A | 39 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0002g0032 others(36): Show |
41 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.-14-4128G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950017 | |||||||
| chr12:26950213 | G | GT | 19 | a0001c0001t0001g0060 a0001c0001t0002g0001 a0001c0001t0002g0040 others(16): Show |
39 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.-14-3906dupT | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTT | 12 | a0001c0001t0002g0010 a0001c0001t0002g0150 a0001c0001t0002g0153 others(9): Show |
18 | HG00639.hp1 HG00741.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-14-3907_-14-3906d others(4): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTT | 19 | a0001c0001t0001g0036 a0001c0001t0001g0089 a0001c0001t0001g0111 others(16): Show |
23 | HG00140.hp1 HG00735.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-14-3909_-14-3906d others(6): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTT | 49 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0018 others(46): Show |
66 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.-14-3910_-14-3906d others(7): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTT | 50 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(47): Show |
69 | HG00323.hp2 HG00597.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-14-3911_-14-3906d others(8): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT | 35 | a0001c0001t0001g0016 a0001c0001t0001g0108 a0001c0001t0001g0109 others(32): Show |
40 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-14-3912_-14-3906d others(9): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT others(1): Show |
24 | a0001c0001t0001g0006 a0001c0001t0001g0123 a0001c0001t0001g0218 others(21): Show |
36 | HG00099.hp1 HG00544.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-14-3913_-14-3906d others(10): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT others(2): Show |
15 | a0001c0001t0001g0011 a0001c0001t0001g0056 a0001c0001t0001g0087 others(12): Show |
23 | HG00621.hp1 HG01074.hp1 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.-14-3914_-14-3906d others(11): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT others(3): Show |
9 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0085 others(6): Show |
13 | HG00280.hp2 HG00673.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14-3915_-14-3906d others(12): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT others(4): Show |
7 | a0001c0001t0001g0266 a0001c0001t0003g0068 a0001c0001t0003g0131 others(4): Show |
10 | HG02257.hp1 HG03139.hp1 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-3916_-14-3906d others(13): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT others(5): Show |
3 | a0001c0001t0004g0050 a0001c0001t0017g0125 a0001c0001t0024g0212 |
4 | HG03540.hp2 NA18962.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-3917_-14-3906d others(14): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT others(6): Show |
8 | a0001c0001t0003g0029 a0001c0001t0003g0069 a0001c0001t0003g0070 others(5): Show |
9 | HG00099.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-3918_-14-3906d others(15): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT others(7): Show |
14 | a0001c0001t0001g0198 a0001c0001t0003g0008 a0001c0001t0003g0017 others(11): Show |
23 | HG01109.hp1 HG02074.hp2 HG02523.hp1 others(20): Show |
intron_variant | MODIFIER | c.-14-3919_-14-3906d others(16): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT others(8): Show |
13 | a0001c0001t0003g0002 a0001c0001t0003g0031 a0001c0001t0003g0064 others(10): Show |
23 | HG00642.hp1 HG01358.hp1 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-14-3920_-14-3906d others(17): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT others(9): Show |
4 | a0001c0001t0003g0038 a0001c0001t0003g0224 a0001c0001t0010g0134 others(1): Show |
5 | HG03041.hp1 NA18947.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-3921_-14-3906d others(18): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0014g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-14-3922_-14-3906d others(19): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT others(13): Show |
1 | a0001c0001t0003g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-14-3925_-14-3906d others(22): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT others(16): Show |
1 | a0001c0001t0003g0063 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-14-3928_-14-3906d others(25): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT others(19): Show |
1 | a0001c0001t0003g0078 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-14-3931_-14-3906d others(28): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950213 | G | GTTTTTTT others(23): Show |
1 | a0001c0001t0018g0086 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-3906_-14-3905i others(32): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26950213 | ||||||
| chr12:26950274 | G | A | 1 | a0001c0001t0011g0222 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-14-3871G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950274 | |||||||
| chr12:26950376 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-14-3769C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950376 | |||||||
| chr12:26950379 | C | G | 1 | a0001c0001t0005g0220 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-14-3766C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950379 | |||||||
| chr12:26950381 | C | G | 1 | a0001c0001t0027g0137 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-14-3764C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950381 | |||||||
| chr12:26950445 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-14-3700C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950445 | |||||||
| chr12:26950472 | C | T | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0039 others(23): Show |
28 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14-3673C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950472 | |||||||
| chr12:26950516 | G | A | 43 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(40): Show |
57 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.-14-3629G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950516 | |||||||
| chr12:26950591 | G | C | 2 | a0001c0001t0004g0283 a0001c0001t0004g0284 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-14-3554G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950591 | |||||||
| chr12:26950612 | C | G | 4 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0064 others(1): Show |
9 | NA18943.hp1 NA18967.hp2 NA18979.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-3533C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950612 | |||||||
| chr12:26950655 | A | G | 43 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(40): Show |
57 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.-14-3490A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950655 | |||||||
| chr12:26950789 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-14-3356A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950789 | |||||||
| chr12:26950814 | T | C | 36 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0002g0032 others(33): Show |
38 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.-14-3331T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950814 | |||||||
| chr12:26950895 | G | A | 3 | a0001c0001t0003g0063 a0001c0001t0012g0043 a0001c0001t0014g0062 |
4 | HG02257.hp1 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-3250G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950895 | |||||||
| chr12:26950965 | A | G | 1 | a0001c0001t0027g0137 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-14-3180A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950965 | |||||||
| chr12:26950980 | A | G | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0039 others(23): Show |
28 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14-3165A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26950980 | |||||||
| chr12:26951046 | G | T | 3 | a0001c0001t0007g0009 a0001c0001t0007g0019 a0001c0001t0007g0103 |
9 | HG02451.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-14-3099G>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26951046 | |||||||
| chr12:26951148 | AT | A | 60 | a0001c0001t0001g0106 a0001c0001t0001g0231 a0001c0001t0001g0232 others(57): Show |
63 | HG00597.hp2 HG00738.hp1 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.-14-2985delT | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26951148 | ||||||
| chr12:26951191 | C | G | 1 | a0001c0001t0002g0149 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-14-2954C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26951191 | |||||||
| chr12:26951257 | C | T | 2 | a0001c0001t0002g0168 a0001c0001t0002g0274 |
2 | HG01243.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-14-2888C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26951257 | |||||||
| chr12:26951277 | A | T | 2 | a0001c0001t0001g0051 a0001c0001t0002g0051 |
2 | HG00140.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-14-2868A>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26951277 | |||||||
| chr12:26951434 | C | A | 2 | a0001c0001t0006g0278 a0001c0001t0006g0279 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-14-2711C>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26951434 | |||||||
| chr12:26951476 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14-2669C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26951476 | |||||||
| chr12:26951477 | G | A | 2 | a0001c0001t0013g0171 a0001c0001t0018g0086 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-14-2668G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26951477 | |||||||
| chr12:26951801 | T | A | 1 | a0001c0001t0001g0265 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-14-2344T>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26951801 | |||||||
| chr12:26951961 | A | G | 1 | a0001c0001t0005g0188 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-14-2184A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26951961 | |||||||
| chr12:26952015 | A | G | 1 | a0001c0001t0003g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-14-2130A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952015 | |||||||
| chr12:26952049 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-14-2096G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952049 | |||||||
| chr12:26952072 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14-2073A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952072 | |||||||
| chr12:26952087 | C | CT | 7 | a0001c0001t0001g0060 a0001c0001t0002g0162 a0001c0001t0002g0217 others(4): Show |
8 | HG00738.hp2 HG01496.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14-2038dupT | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26952087 | ||||||
| chr12:26952087 | CT | C | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.-14-2038delT | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26952087 | ||||||
| chr12:26952087 | CTT | C | 8 | a0001c0001t0001g0258 a0001c0001t0001g0266 a0001c0001t0002g0135 others(5): Show |
8 | HG02293.hp2 HG02451.hp2 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-2039_-14-2038d others(4): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26952087 | ||||||
| chr12:26952206 | A | G | 1 | a0001c0001t0002g0271 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-14-1939A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952206 | |||||||
| chr12:26952210 | A | G | 4 | a0001c0001t0002g0033 a0001c0001t0002g0090 a0001c0001t0002g0097 others(1): Show |
5 | HG02135.hp2 NA18966.hp1 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-1935A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952210 | |||||||
| chr12:26952254 | T | C | 10 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0002g0147 others(7): Show |
10 | HG00597.hp2 NA18939.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-1891T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952254 | |||||||
| chr12:26952296 | T | TG | 36 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0002g0032 others(33): Show |
38 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.-14-1848dupG | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26952296 | ||||||
| chr12:26952332 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-14-1813C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952332 | |||||||
| chr12:26952378 | G | A | 1 | a0001c0001t0027g0137 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-14-1767G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952378 | |||||||
| chr12:26952477 | T | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(116): Show |
183 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.-14-1668T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952477 | |||||||
| chr12:26952545 | G | C | 2 | a0001c0001t0003g0063 a0001c0001t0014g0062 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-14-1600G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952545 | |||||||
| chr12:26952675 | CT | C | 30 | a0001c0001t0001g0173 a0001c0001t0001g0216 a0001c0001t0003g0248 others(27): Show |
36 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.-14-1455delT | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26952675 | ||||||
| chr12:26952693 | A | G | 3 | a0001c0001t0010g0132 a0001c0001t0010g0133 a0001c0001t0010g0134 |
3 | HG02723.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-14-1452A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952693 | |||||||
| chr12:26952736 | G | A | 3 | a0001c0001t0001g0231 a0001c0001t0002g0147 a0001c0001t0002g0233 |
3 | NA18939.hp2 NA19007.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-14-1409G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952736 | |||||||
| chr12:26952766 | C | A | 1 | a0001c0001t0001g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-14-1379C>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952766 | |||||||
| chr12:26952822 | A | T | 1 | a0001c0001t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14-1323A>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952822 | |||||||
| chr12:26952988 | C | A | 1 | a0001c0001t0005g0247 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-14-1157C>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952988 | |||||||
| chr12:26952991 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-14-1154G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26952991 | |||||||
| chr12:26953026 | G | A | 1 | a0001c0001t0006g0282 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-14-1119G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26953026 | |||||||
| chr12:26953125 | G | A | 46 | a0001c0001t0001g0198 a0001c0001t0003g0002 a0001c0001t0003g0008 others(43): Show |
67 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(64): Show |
intron_variant | MODIFIER | c.-14-1020G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26953125 | |||||||
| chr12:26953167 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14-978G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26953167 | |||||||
| chr12:26953180 | C | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(120): Show |
187 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.-14-965C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26953180 | |||||||
| chr12:26953220 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-14-925C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26953220 | |||||||
| chr12:26953224 | G | A | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(255): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-14-921G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26953224 | |||||||
| chr12:26953268 | C | CA | 23 | a0001c0001t0001g0107 a0001c0001t0001g0218 a0001c0001t0001g0219 others(20): Show |
23 | HG00621.hp2 HG00733.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.-14-856dupA | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26953268 | ||||||
| chr12:26953268 | CA | C | 209 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(206): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-14-856delA | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26953268 | ||||||
| chr12:26953310 | G | GAGGGTA | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(119): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.-14-832_-14-827dup others(6): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26953310 | ||||||
| chr12:26953327 | T | TCAGGAGA others(3): Show |
1 | a0001c0001t0004g0205 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-14-817_-14-808dup others(10): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 26953327 | ||||||
| chr12:26953421 | T | C | 4 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0064 others(1): Show |
9 | NA18943.hp1 NA18967.hp2 NA18979.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-724T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26953421 | |||||||
| chr12:26953516 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-14-629G>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26953516 | |||||||
| chr12:26953542 | C | G | 1 | a0001c0001t0004g0211 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-14-603C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26953542 | |||||||
| chr12:26953547 | A | G | 1 | a0001c0001t0018g0086 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-14-598A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26953547 | |||||||
| chr12:26953607 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-14-538A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26953607 | |||||||
| chr12:26953620 | A | T | 1 | a0001c0001t0002g0152 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-14-525A>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26953620 | |||||||
| chr12:26953875 | G | A | 40 | a0001c0001t0001g0198 a0001c0001t0003g0002 a0001c0001t0003g0008 others(37): Show |
61 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.-14-270G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26953875 | |||||||
| chr12:26954080 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-14-65C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 1/6 | chr12 | 26954080 | |||||||
| chr12:26954335 | G | A | 20 | a0001c0001t0004g0045 a0001c0001t0004g0105 a0001c0001t0004g0281 others(17): Show |
21 | HG01123.hp2 HG01167.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+42G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26954335 | |||||||
| chr12:26954518 | A | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0106 a0001c0001t0001g0108 |
4 | NA19006.hp2 NA19012.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+225A>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26954518 | |||||||
| chr12:26954573 | A | G | 3 | a0001c0001t0010g0132 a0001c0001t0010g0133 a0001c0001t0010g0134 |
3 | HG02723.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.135+280A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26954573 | |||||||
| chr12:26954780 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.135+487C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26954780 | |||||||
| chr12:26954783 | A | G | 2 | a0001c0001t0005g0185 a0001c0001t0005g0277 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.135+490A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26954783 | |||||||
| chr12:26954953 | A | G | 1 | a0001c0001t0013g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.135+660A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26954953 | |||||||
| chr12:26954976 | T | G | 1 | a0001c0001t0003g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.135+683T>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26954976 | |||||||
| chr12:26955061 | T | A | 2 | a0001c0001t0003g0079 a0001c0001t0003g0080 |
2 | HG02698.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.135+768T>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26955061 | |||||||
| chr12:26955070 | A | T | 2 | a0001c0001t0003g0031 a0001c0001t0003g0239 |
3 | HG02071.hp1 HG02129.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.135+777A>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26955070 | |||||||
| chr12:26955123 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.135+830G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26955123 | |||||||
| chr12:26955178 | T | C | 1 | a0001c0001t0008g0252 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.135+885T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26955178 | |||||||
| chr12:26955189 | G | C | 1 | a0001c0001t0002g0164 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.135+896G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26955189 | |||||||
| chr12:26955328 | T | C | 40 | a0001c0001t0001g0198 a0001c0001t0003g0002 a0001c0001t0003g0008 others(37): Show |
61 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.135+1035T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26955328 | |||||||
| chr12:26955519 | A | T | 1 | a0001c0001t0004g0204 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.136-1024A>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26955519 | |||||||
| chr12:26955629 | A | G | 3 | a0001c0001t0010g0132 a0001c0001t0010g0133 a0001c0001t0010g0134 |
3 | HG02723.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.136-914A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26955629 | |||||||
| chr12:26955942 | G | C | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0039 others(23): Show |
28 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.136-601G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26955942 | |||||||
| chr12:26956018 | A | AT | 38 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0002g0032 others(35): Show |
42 | HG00597.hp2 HG01071.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.136-513dupT | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 26956018 | ||||||
| chr12:26956030 | T | A | 3 | a0001c0001t0010g0132 a0001c0001t0010g0133 a0001c0001t0010g0134 |
3 | HG02723.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.136-513T>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26956030 | |||||||
| chr12:26956031 | A | T | 1 | a0001c0001t0012g0043 | 2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.136-512A>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26956031 | |||||||
| chr12:26956165 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.136-378G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26956165 | |||||||
| chr12:26956186 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.136-357T>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26956186 | |||||||
| chr12:26956283 | A | T | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0039 others(23): Show |
28 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.136-260A>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26956283 | |||||||
| chr12:26956318 | A | G | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0039 others(23): Show |
28 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.136-225A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26956318 | |||||||
| chr12:26956479 | C | CAT | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(77): Show |
130 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.136-43_136-42dupAT | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 26956479 | ||||||
| chr12:26956479 | C | CATAT | 35 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0198 others(32): Show |
49 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.136-45_136-42dupAT others(2): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 26956479 | ||||||
| chr12:26956479 | C | CATATAT | 7 | a0001c0001t0004g0201 a0001c0001t0004g0204 a0001c0001t0004g0236 others(4): Show |
7 | HG01928.hp1 HG01943.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-47_136-42dupAT others(4): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 26956479 | ||||||
| chr12:26956479 | CAT | C | 92 | a0001c0001t0001g0085 a0001c0001t0001g0216 a0001c0001t0001g0231 others(89): Show |
100 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.136-43_136-42delAT | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 26956479 | ||||||
| chr12:26956502 | T | A | 1 | a0001c0001t0001g0258 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.136-41T>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 2/6 | chr12 | 26956502 | |||||||
| chr12:26956722 | A | G | 22 | a0001c0001t0004g0045 a0001c0001t0004g0105 a0001c0001t0004g0281 others(19): Show |
23 | HG00738.hp1 HG01123.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.253+62A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26956722 | |||||||
| chr12:26956760 | G | A | 2 | a0001c0001t0009g0054 a0001c0001t0009g0055 |
4 | HG02572.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.253+100G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26956760 | |||||||
| chr12:26956842 | CT | C | 32 | a0001c0001t0001g0173 a0001c0001t0001g0216 a0001c0001t0005g0015 others(29): Show |
38 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.253+183delT | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26956842 | |||||||
| chr12:26956941 | A | G | 2 | a0001c0001t0003g0127 a0001c0001t0011g0129 |
2 | NA18951.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.253+281A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26956941 | |||||||
| chr12:26956945 | G | A | 2 | a0001c0001t0009g0054 a0001c0001t0009g0055 |
4 | HG02572.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.253+285G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26956945 | |||||||
| chr12:26956955 | T | C | 5 | a0001c0001t0004g0023 a0001c0001t0004g0206 a0001c0001t0004g0209 others(2): Show |
7 | NA18970.hp2 NA18981.hp1 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.253+295T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26956955 | |||||||
| chr12:26956971 | A | T | 39 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0017 others(36): Show |
60 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.253+311A>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26956971 | |||||||
| chr12:26957031 | T | C | 1 | a0001c0001t0002g0141 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.253+371T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26957031 | |||||||
| chr12:26957068 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.253+408C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26957068 | |||||||
| chr12:26957090 | A | G | 22 | a0001c0001t0004g0045 a0001c0001t0004g0105 a0001c0001t0004g0281 others(19): Show |
23 | HG00738.hp1 HG01123.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.253+430A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26957090 | |||||||
| chr12:26957094 | C | G | 42 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0017 others(39): Show |
63 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.253+434C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26957094 | |||||||
| chr12:26957150 | C | T | 1 | a0001c0001t0003g0072 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.254-451C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26957150 | |||||||
| chr12:26957202 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.254-399T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26957202 | |||||||
| chr12:26957282 | A | G | 1 | a0001c0001t0002g0138 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.254-319A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26957282 | |||||||
| chr12:26957299 | A | T | 1 | a0001c0001t0005g0180 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.254-302A>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26957299 | |||||||
| chr12:26957475 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0113 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.254-126A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26957475 | |||||||
| chr12:26957496 | G | C | 1 | a0001c0001t0002g0061 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.254-105G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 3/6 | chr12 | 26957496 | |||||||
| chr12:26957752 | T | G | 2 | a0001c0001t0013g0171 a0001c0001t0018g0086 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.396+9T>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26957752 | |||||||
| chr12:26957982 | G | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0002g0217 |
3 | HG02257.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.396+239G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26957982 | |||||||
| chr12:26958017 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.396+274A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26958017 | |||||||
| chr12:26958023 | G | T | 1 | a0001c0001t0002g0143 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.396+280G>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26958023 | |||||||
| chr12:26958106 | A | G | 1 | a0001c0001t0002g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.396+363A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26958106 | |||||||
| chr12:26958131 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.396+388C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26958131 | |||||||
| chr12:26958212 | T | C | 1 | a0001c0001t0005g0228 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.396+469T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26958212 | |||||||
| chr12:26958388 | C | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(255): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.396+645C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26958388 | |||||||
| chr12:26958403 | A | C | 1 | a0001c0001t0003g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.396+660A>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26958403 | |||||||
| chr12:26958545 | A | G | 1 | a0001c0001t0003g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.396+802A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26958545 | |||||||
| chr12:26958609 | A | G | 41 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0017 others(38): Show |
62 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(59): Show |
intron_variant | MODIFIER | c.396+866A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26958609 | |||||||
| chr12:26958859 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.396+1116G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26958859 | |||||||
| chr12:26958907 | A | G | 28 | a0001c0001t0001g0173 a0001c0001t0001g0216 a0001c0001t0005g0015 others(25): Show |
33 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.396+1164A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26958907 | |||||||
| chr12:26958931 | T | G | 1 | a0001c0001t0005g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.396+1188T>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26958931 | |||||||
| chr12:26959027 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.396+1284C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26959027 | |||||||
| chr12:26959033 | C | G | 61 | a0001c0001t0004g0005 a0001c0001t0004g0022 a0001c0001t0004g0023 others(58): Show |
76 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.396+1290C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26959033 | |||||||
| chr12:26959035 | A | G | 1 | a0001c0001t0005g0230 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.396+1292A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26959035 | |||||||
| chr12:26959050 | C | G | 262 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(259): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.396+1307C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26959050 | |||||||
| chr12:26959174 | ATAAAT | A | 3 | a0001c0001t0010g0132 a0001c0001t0010g0133 a0001c0001t0010g0134 |
3 | HG02723.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.397-1331_397-1327d others(7): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 26959174 | ||||||
| chr12:26959686 | A | G | 7 | a0001c0001t0002g0083 a0001c0001t0002g0138 a0001c0001t0002g0140 others(4): Show |
7 | HG01109.hp2 HG01928.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.397-829A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26959686 | |||||||
| chr12:26959848 | A | G | 1 | a0001c0001t0010g0133 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.397-667A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26959848 | |||||||
| chr12:26959914 | A | C | 1 | a0001c0001t0006g0193 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.397-601A>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26959914 | |||||||
| chr12:26959926 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.397-589G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26959926 | |||||||
| chr12:26960170 | C | CCTAAACA others(184): Show |
1 | a0001c0001t0018g0086 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.397-325_397-324ins others(191): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 26960170 | ||||||
| chr12:26960288 | C | T | 1 | a0001c0001t0004g0287 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.397-227C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26960288 | |||||||
| chr12:26960323 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.397-192T>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 4/6 | chr12 | 26960323 | |||||||
| chr12:26960725 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.510+97G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26960725 | |||||||
| chr12:26960734 | T | C | 5 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0073 others(2): Show |
7 | NA18967.hp1 NA18972.hp1 NA19063.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+106T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26960734 | |||||||
| chr12:26960749 | G | T | 1 | a0001c0001t0001g0056 | 2 | HG02015.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.510+121G>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26960749 | |||||||
| chr12:26960771 | A | G | 2 | a0001c0001t0003g0063 a0001c0001t0014g0062 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.510+143A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26960771 | |||||||
| chr12:26960816 | G | A | 2 | a0001c0001t0013g0171 a0001c0001t0018g0086 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.510+188G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26960816 | |||||||
| chr12:26960913 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.510+285A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26960913 | |||||||
| chr12:26961062 | T | C | 40 | a0001c0001t0001g0198 a0001c0001t0003g0002 a0001c0001t0003g0008 others(37): Show |
61 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.510+434T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26961062 | |||||||
| chr12:26961082 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 |
3 | HG01496.hp1 HG03491.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.510+454A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26961082 | |||||||
| chr12:26961246 | G | A | 43 | a0001c0001t0001g0198 a0001c0001t0003g0002 a0001c0001t0003g0008 others(40): Show |
64 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.510+618G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26961246 | |||||||
| chr12:26961391 | C | G | 43 | a0001c0001t0001g0198 a0001c0001t0003g0002 a0001c0001t0003g0008 others(40): Show |
64 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.510+763C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26961391 | |||||||
| chr12:26961599 | G | A | 1 | a0001c0001t0006g0278 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.510+971G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26961599 | |||||||
| chr12:26961673 | G | A | 1 | a0001c0001t0003g0076 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.510+1045G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26961673 | |||||||
| chr12:26961719 | C | T | 1 | a0001c0001t0027g0137 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.510+1091C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26961719 | |||||||
| chr12:26961735 | T | C | 1 | a0001c0001t0004g0206 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.510+1107T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26961735 | |||||||
| chr12:26962092 | C | T | 1 | a0001c0001t0008g0251 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.511-1250C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26962092 | |||||||
| chr12:26962113 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.511-1229G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26962113 | |||||||
| chr12:26962200 | A | G | 40 | a0001c0001t0001g0198 a0001c0001t0003g0002 a0001c0001t0003g0008 others(37): Show |
61 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.511-1142A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26962200 | |||||||
| chr12:26962408 | T | G | 2 | a0001c0001t0001g0198 a0001c0001t0003g0199 |
2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.511-934T>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26962408 | |||||||
| chr12:26962462 | C | T | 238 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(235): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.511-880C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26962462 | |||||||
| chr12:26962522 | C | G | 1 | a0001c0001t0014g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.511-820C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26962522 | |||||||
| chr12:26962522 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.511-820C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26962522 | |||||||
| chr12:26962529 | C | T | 1 | a0001c0001t0003g0074 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.511-813C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26962529 | |||||||
| chr12:26962619 | CTGT | C | 28 | a0001c0001t0001g0173 a0001c0001t0001g0216 a0001c0001t0005g0015 others(25): Show |
33 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.511-718_511-716del others(3): Show |
FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr12 | 26962619 | ||||||
| chr12:26962699 | C | T | 2 | a0001c0001t0004g0202 a0001c0001t0004g0203 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.511-643C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26962699 | |||||||
| chr12:26962717 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.511-625G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26962717 | |||||||
| chr12:26962771 | T | C | 20 | a0001c0001t0001g0216 a0001c0001t0005g0015 a0001c0001t0005g0021 others(17): Show |
25 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.511-571T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26962771 | |||||||
| chr12:26962985 | T | G | 1 | a0001c0001t0005g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.511-357T>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26962985 | |||||||
| chr12:26963014 | C | T | 28 | a0001c0001t0001g0173 a0001c0001t0001g0216 a0001c0001t0005g0015 others(25): Show |
33 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.511-328C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26963014 | |||||||
| chr12:26963044 | C | T | 2 | a0002c0002t0002g0020 a0002c0002t0002g0165 |
4 | NA18942.hp1 NA18986.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-298C>T | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26963044 | |||||||
| chr12:26963315 | T | G | 2 | a0001c0001t0004g0048 a0001c0001t0004g0204 |
3 | HG01074.hp1 HG01952.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.511-27T>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 5/6 | chr12 | 26963315 | |||||||
| chr12:26963812 | C | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0002g0217 |
3 | HG02257.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.624+357C>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 6/6 | chr12 | 26963812 | |||||||
| chr12:26963814 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.624+359T>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 6/6 | chr12 | 26963814 | |||||||
| chr12:26963989 | G | A | 2 | a0001c0001t0003g0063 a0001c0001t0014g0062 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.624+534G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 6/6 | chr12 | 26963989 | |||||||
| chr12:26964366 | A | G | 2 | a0001c0001t0013g0171 a0001c0001t0018g0086 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.625-230A>G | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 6/6 | chr12 | 26964366 | |||||||
| chr12:26964449 | G | C | 37 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0002g0001 others(34): Show |
60 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.625-147G>C | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 6/6 | chr12 | 26964449 | |||||||
| chr12:26964493 | G | A | 1 | a0001c0001t0009g0054 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.625-103G>A | FGFR1OP2 | ENSG00000111790.14 | transcript | ENST00000229395.8 | protein_coding | 6/6 | chr12 | 26964493 |